Description
					Department Description:

Quality Control (QC) is responsible for incoming inspection of components and raw materials, plus quality testing (e.g. analytical, microbiological) of intermediate, stability and final product samples to demonstrate that all products manufactured meet standards required for cGMP operations. Various techniques (e.g. assay transfers, validation and qualification of new instrumentation) are utilized within the Quality Control Laboratory to ensure cGMP compliance.

Position Summary:

Perform routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation.

DUTIES AND RESPONSIBILITIES

Essential Functions: 

Run and execute PCR and PCR techniques 
Perform microbiological assays for in-process and final product samples.
Perform analytical methods for final bulk material/finished goods.
Test and disposition of raw materials and perform environmental monitoring.
Review of QC data for compliance to procedures and specifications.
Calculate and evaluate results.
Participate in lab maintenance and administration duties.
Initiate lab investigations and deviations.
Lab support including but not limited to glass washing, autoclaving, etc.
Effectively demonstrate an understanding of CGMPs and how it applies to specific responsibilities.
Follow accurate oral and written procedures for testing of in-process and final product samples.
										Skills
					GMP, PCR, Sample testing, Quality control, microbiology, qPCR, cell culture, mammalian cell culture, Qc, Biology, Cgmp
										Top Skills Details
					GMP,PCR,Sample testing,Quality control,microbiology,qPCR,cell culture,mammalian cell culture
										Additional Skills &amp; Qualifications
					BS 3+ years or MS 2-4 years experience in microbiology, biology, or similar life science
Experience with QC bioassays particularly utilizing PCR
Experience with microbiological testing, biological assays, or environmental monitoring
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Permanent position based out of Cambridge, MA.Pay and BenefitsThe pay range for this position is $70000.00 - $83200.00/yr.They will get Restricted stock units, holiday, vacationWorkplace TypeThis is a fully onsite position in Cambridge,MA.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

public

Quality Control Analyst

QC Lab Analyst3rd shift 4-10s (M-Thur)Job DescriptionThis role focuses on performing routine and project-based qPCR testing to support in-process and finished product quality control in a GMP pharmaceutical environment. The Quality Control Analyst conducts time-sensitive qPCR assays, handles raw material and finished product samples, supports method validation and development, and contributes to environmental and contaminant monitoring in a brand-new laboratory operating around the clock.Responsibilities<ul><li>Perform routine qPCR testing on samples with a 7-hour turnaround time, working in parallel with another analyst to ensure timely completion.</li><li>Conduct in-process testing on raw materials, primarily pig-origin tissue slurries, including extraction of RNA from tissue samples.</li><li>Perform finished product testing on final drug product and select specialty products, including some testing for additional sites.</li><li>Run speciation assays to identify and quantify different species within a sample.</li><li>Carry out contaminant monitoring and positive control environmental monitoring while samples are running.</li><li>Perform calibration and routine maintenance of laboratory instruments, including centrifuges, spectrophotometers, and liquid handler robots.</li><li>Prepare reagents, manage inventory, and ensure that all necessary materials are available and properly documented.</li><li>Support validation activities, including validating basic centrifuges, spectrophotometers, liquid handler robots, laboratory software, and lab spaces.</li><li>Assist with software programming related to qPCR and laboratory instruments as part of validation and method support.</li><li>Draft and support laboratory methods, including method development and documentation in accordance with GMP and FDA expectations.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associates or Bachelor’s degree in Microbiology or a related discipline preferred for all levels.</li><li>High School Diploma or G.E.D. required for all levels.</li><li>Minimum of 1 year of working in a regulated laboratory environment.</li><li>Experience with pipettes required.</li><li>PCR experience from school or industry is preferred but not required.</li><li>Open to different experience levels: Associate, Analyst, and Sr</li></ul>Work EnvironmentThe role is on third shift, Monday through Thursday, working 10-hour days starting at 9:00 p.m. Job Type &amp; LocationThis is a Permanent position based out of Madison, WI.Pay and BenefitsThe pay range for this position is $45760.00 - $75000.00/yr.Competitive compensation; excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&amp;D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; 401kWorkplace TypeThis is a fully onsite position in Madison,WI.Application DeadlineThis position is anticipated to close on Aug 6, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Description
					Department Description:

Quality Control (QC) is responsible for incoming inspection of components and raw materials, plus quality testing (e.g. analytical, microbiological) of intermediate, stability and final product samples to demonstrate that all products manufactured meet standards required for cGMP operations. Various techniques (e.g. assay transfers, validation and qualification of new instrumentation) are utilized within the Quality Control Laboratory to ensure cGMP compliance.

Position Summary:

Perform routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation.

DUTIES AND RESPONSIBILITIES

Essential Functions: 

Run and execute PCR and PCR techniques 
Perform microbiological assays for in-process and final product samples.
Perform analytical methods for final bulk material/finished goods.
Test and disposition of raw materials and perform environmental monitoring.
Review of QC data for compliance to procedures and specifications.
Calculate and evaluate results.
Participate in lab maintenance and administration duties.
Initiate lab investigations and deviations.
Lab support including but not limited to glass washing, autoclaving, etc.
Effectively demonstrate an understanding of CGMPs and how it applies to specific responsibilities.
Follow accurate oral and written procedures for testing of in-process and final product samples.
										Skills
					GMP, PCR, Sample testing, Quality control, microbiology, qPCR, cell culture, mammalian cell culture, Qc, Biology, Cgmp
										Top Skills Details
					GMP,PCR,Sample testing,Quality control,microbiology,qPCR,cell culture,mammalian cell culture
										Additional Skills &amp; Qualifications
					BS 3+ years or MS 2-4 years experience in microbiology, biology, or similar life science
Experience with QC bioassays particularly utilizing PCR
Experience with microbiological testing, biological assays, or environmental monitoring
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Permanent position based out of Cambridge, MA.Pay and BenefitsThe pay range for this position is $70000.00 - $83200.00/yr.They will get Restricted stock units, holiday, vacationWorkplace TypeThis is a fully onsite position in Cambridge,MA.Application DeadlineThis position is anticipated to close on Aug 7, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

DescriptionQuality Control (QC) is responsible for incoming inspection of components and raw materials, plus quality testing (e.g. analytical, microbiological) of intermediate, stability and final product samples to demonstrate that all products manufactured meet standards required for cGMP operations. Various techniques (e.g. assay transfers, validation and qualification of new instrumentation) are utilized within the Quality Control Laboratory to ensure cGMP compliance.Position Summary:Perform routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation.DUTIES AND RESPONSIBILITIESEssential Functions: Run and execute PCR and PCR techniques Perform microbiological assays for in-process and final product samples.Perform analytical methods for final bulk material/finished goods.Test and disposition of raw materials and perform environmental monitoring.Review of QC data for compliance to procedures and specifications.Calculate and evaluate results.Participate in lab maintenance and administration duties.Initiate lab investigations and deviations.Lab support including but not limited to glass washing, autoclaving, etc.Effectively demonstrate an understanding of CGMPs and how it applies to specific responsibilities.Follow accurate oral and written procedures for testing of in-process and final product samples.Additional Skills &amp; QualificationsBS 3+ years or MS 2-4 years experience in microbiology, biology, or similar life scienceExperience with QC bioassays particularly utilizing PCRExperience with microbiological testing, biological assays, or environmental monitoringJob Type &amp; LocationThis is a Contract to Hire position based out of Cambridge, MA.Pay and BenefitsThe pay range for this position is $35.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Cambridge,MA.Application DeadlineThis position is anticipated to close on Aug 7, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Analyst-Molecular Bio

Job Title: Quality Control Chemist / QC Lab TechnicianJob DescriptionThis role supports a fast-paced quality laboratory by performing routine and non-routine testing on raw materials and production batches to ensure products meet strict quality standards. The Quality Control Chemist conducts quantitative and qualitative analytical tests, evaluates results against specifications, and supports continuous improvement by researching technical literature and assessing existing processes. The position offers strong growth potential, with opportunities to move into areas such as research and development, project engineering, and leadership roles within a global provider of cleaning, sanitizing, and maintenance products.Responsibilities<ul><li>Perform batch testing, raw material testing, and batch adjustment calculations for all assigned materials.</li><li>Evaluate test results and approve batches that meet established acceptance-testing specifications.</li><li>Conduct laboratory tests including specific gravity, pH, viscosity, HPLC, GC, and other analytical methods in accordance with standard procedures.</li><li>Prepare reagents and samples for analytical testing to ensure accurate and reliable results.</li><li>Record test data accurately and concisely in ERP systems such as SAP, maintaining complete and traceable documentation.</li><li>Perform daily and weekly calibrations and method assurance checks for laboratory instruments to ensure ongoing accuracy.</li><li>Maintain and follow Standard Operating Procedures (SOPs) and ensure compliance with Good Manufacturing Practices (GMP) protocols.</li><li>Assist in maintaining the productivity, organization, and cleanliness of a fast-paced production laboratory.</li><li>Support quality activities during customer and regulatory audits by providing documentation, data, and technical explanations.</li><li>Actively participate and collaborate with Quality team members to resolve issues, improve processes, and support overall quality objectives.</li><li>Maintain a professional working relationship with production associates and other cross-functional partners.</li><li>Research technical literature and evaluate existing processes to identify opportunities for improvement or optimization.</li><li>Set up and operate specialized laboratory instruments by following manufacturers’ instructions with limited supervision.</li><li>Use a variety of laboratory glassware and instruments that require a high degree of technical skill and attention to detail.</li><li>Assume full responsibility for minor laboratory or quality-related projects as assigned.</li></ul>Essential Skills<ul><li>Bachelor’s degree, preferably in Chemistry or Chemical Engineering; degrees in Biology, Food Science, or other technical disciplines are also considered.</li><li>At least 2 years of experience in plant quality control practices and wet chemistry.</li><li>At least 1–2 years of experience with GC or HPLC instrumentation.</li><li>At least 1–2 years of experience performing pH measurements in a laboratory setting.</li><li>Hands-on experience in quality control, analytical chemistry, and wet chemistry techniques.</li><li>Working knowledge of Good Manufacturing Practices (GMP).</li><li>Knowledge of basic statistical principles as applied to quality control and data analysis.</li><li>Training or experience with HPLC, GC, FTIR, or other analytical instruments.</li><li>Knowledge of quality control practices and quality assurance tools.</li><li>Familiarity and experience with ISO-9000 certification requirements and practices.</li><li>Experience in the specialty chemical industry or related industries such as food processing, pharmaceuticals, or health and hygiene products.</li><li>Experience working with detergent chemistry, including raw materials and finished goods relevant to cleaning and sanitizing products.</li><li>Ability to accurately record and manage data in ERP systems such as SAP.</li><li>Ability to follow detailed SOPs and technical instructions with minimal supervision.</li><li>Strong attention to detail, accuracy, and adherence to laboratory safety and quality standards.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience supporting customer and regulatory audits within a laboratory or manufacturing environment.</li><li>Demonstrated ability to work effectively in a fast-paced production laboratory while maintaining high quality standards.</li><li>Strong organizational skills to manage multiple tests, samples, and documentation simultaneously.</li><li>Effective communication skills to collaborate with quality, production, and other cross-functional teams.</li><li>Ability to research technical literature and evaluate existing processes for potential improvements.</li><li>Interest in career growth within quality, R&amp;D, project engineering, or leadership roles in a technical environment.</li></ul>Work EnvironmentThis position is based in a production quality laboratory that supports a global portfolio of cleaning, sanitizing, and maintenance products for hospitality, institutional, and industrial markets. The role involves hands-on work with laboratory glassware and analytical instruments such as HPLC, GC, FTIR, pH meters, and viscosity measurement devices, requiring a high level of technical skill and precision. The environment is fast-paced and highly structured, with strict adherence to Good Manufacturing Practices, Standard Operating Procedures, and ISO-9000 requirements. Team members collaborate closely with production and quality staff, and may assume responsibility for smaller projects while working with limited supervision. Appropriate laboratory attire and personal protective equipment are required to ensure safety when handling chemicals and operating instruments.Job Type &amp; LocationThis is a Contract to Hire position based out of Martinsburg, WV.Pay and BenefitsThe pay range for this position is $25.00 - $26.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Martinsburg,WV.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Chemist

Job Title: Quality Control ChemistJob DescriptionThe Quality Control Chemist performs routine laboratory testing to ensure that raw materials and products meet established quality standards in an FDA-regulated cGMP environment. This role focuses on wet chemistry techniques, FTIR spectroscopy, and physical property measurements while maintaining accurate documentation in an ERP system and adhering to SOPs, Good Documentation Practices, and laboratory safety protocols.Responsibilities<ul><li>Perform routine wet chemistry testing, including titrations and sample preparation, to evaluate product and raw material quality.</li><li>Conduct raw material identity testing using FTIR spectroscopy, including sample preparation and library matching.</li><li>Determine physical properties of samples, including pH, specific gravity, and viscosity, using appropriate laboratory methods and instrumentation.</li><li>Accurately document all test results, calculations, and raw data in the ERP system in accordance with Good Documentation Practices.</li><li>Follow established Standard Operating Procedures (SOPs) for all testing activities and document any unexpected results or out-of-specification findings.</li><li>Prepare laboratory reagents, standards, and test samples in accordance with method requirements.</li><li>Maintain a clean, organized, and safe laboratory area, including proper handling and storage of chemicals and samples.</li><li>Assist in the preparation of the laboratory for testing activities, ensuring instruments and equipment are ready and calibrated as required.</li><li>Communicate clearly with team members and supervisors regarding test results, issues encountered, and any deviations from expected outcomes.</li><li>Support continuous improvement of laboratory practices by adhering to cGMP requirements and contributing to a culture of quality and safety.</li></ul>Essential Skills<ul><li>Bachelor's degree in chemistry, biochemistry, or a closely related scientific discipline.</li><li>6+ months of industry experience in a laboratory environment, preferably in an FDA-regulated cGMP setting.</li><li>Proficiency in wet chemistry techniques, including titrations and sample preparation.</li><li>Experience performing raw material testing and basic laboratory testing in a quality control setting.</li><li>Ability to operate and interpret results from FTIR instruments for identity testing, or strong aptitude and willingness to learn.</li><li>Solid understanding of Good Documentation Practices (GDP) and laboratory safety protocols.</li><li>Ability to follow written Standard Operating Procedures (SOPs) with strong attention to detail.</li><li>Strong organizational skills and accuracy in recording data, calculations, and observations in an ERP or similar system.</li><li>Ability to work effectively in a laboratory environment as part of a small team.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior experience working in an FDA-regulated cGMP environment.</li><li>Hands-on experience operating FTIR instruments for raw material identity testing.</li><li>Familiarity with ERP systems or laboratory information management systems (LIMS) for data entry and tracking.</li><li>Demonstrated commitment to maintaining high quality standards and compliance with laboratory procedures.</li><li>Strong problem-solving skills and the ability to investigate and document unexpected or out-of-specification results.</li><li>Effective communication skills to collaborate with colleagues and report findings clearly.</li></ul>Work EnvironmentThis position operates on a first shift schedule, typically from 6:00 a.m. to 2:30 p.m. The role is based in a laboratory environment within a small team of approximately six people. The chemist works at laboratory benches and with analytical instruments such as FTIR, pH meters, and equipment for measuring specific gravity and viscosity. The environment emphasizes adherence to cGMP, Good Documentation Practices, and strict laboratory safety protocols. Team members maintain a clean, orderly lab space and follow appropriate laboratory attire and personal protective equipment requirements suitable for handling chemicals and conducting routine testing.Job Type &amp; LocationThis is a Contract position based out of Santa Fe Springs, CA.Pay and BenefitsThe pay range for this position is $25.00 - $27.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Santa Fe Springs,CA.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control ChemistJob DescriptionThe Quality Control Chemist will initially be responsible for conducting physical property testing and wet chemistry testing, such as viscosity, pH, and TOC for water testing. The role will expand to encompass all analytical testing, including HPLC, GC, and more. The individual will prioritize daily sample testing and perform various laboratory tests on bulk formula batches and line samples of raw materials and in-process materials. Additionally, they will review compounding and laboratory records for accuracy and completeness, investigate customer complaints and OOS/OOT results, and implement corrective actions as determined by QC supervision.Responsibilities<ul><li>Perform laboratory analysis on incoming raw materials, in-process samples, and finished products according to established procedures, including wet chemistry, GC, and HPLC.</li><li>Prepare samples for chromatographic analysis and prepare standard and reagent solutions.</li><li>Coordinate information flow within the laboratory and to internal customers.</li><li>Access, input, and retrieve information from the LIMS.</li><li>Dispose of raw materials, process samples, and finished products for use or sale.</li><li>Ensure all laboratory documentation meets standards for completeness and accuracy according to Good Documentation Practices (GDP) and GMP.</li><li>Handle laboratory clean-up and housekeeping duties, including waste disposal and glassware washing.</li><li>Document deviations in performance not anticipated or indicated in test procedures.</li><li>Become proficient in performing routine GC and HPLC analysis, including integration and result calculations.</li><li>Assist with OOS/OOT and customer complaint investigations.</li><li>Assist with method development protocols and conduct requisite testing.</li><li>Assist with IQ/OQ/PQ and instrument validation/calibration tasks.</li><li>Assist with method transfer protocols and requisite testing.</li><li>Assist with annual/new supplier validations protocol, sample transfer, and testing process.</li><li>Assist with SOP creation, review, and revision activities.</li><li>Assist with stability protocol and testing processes.</li><li>Assist with supplies/services ordering process.</li><li>Assist with contract manufacturing protocol and workflow.</li><li>Assist with instrument maintenance and troubleshooting.</li></ul>Essential Skills<ul><li>Strong multi-tasking ability and capability to prioritize or re-prioritize based on changing needs.</li><li>Effective communication skills with compounding (manufacturing) leadership.</li><li>Confidence to work independently without constant supervision.</li><li>Willingness to learn and adapt.</li><li>Ability to work in a high throughput environment within a team dynamic.</li><li>Proficiency in performing repetitive testing quickly and accurately.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's Degree minimum required, Chemistry preferred but open to Biochemistry, Biology with a Chemistry Minor, or other related science.</li><li>Strong preference for 1 year of experience in a QC laboratory with exposure to physical testing, volumetric solution sample preparation, GMP/GDP, and LIMS or other lab sample management systems.</li><li>Entry-level candidates with strong demonstrated chemistry skills will be considered.</li><li>General experience working within MS Office, including Word, Excel, Teams, Outlook, etc.</li></ul>Work EnvironmentThe position is for the third shift, Monday to Friday, from 10:00 PM to 7:00 AM. Initial training will be on the first shift, Monday to Friday, for approximately 2-4 weeks. Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $24.00 - $24.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Aug 4, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control ChemistJob DescriptionThe Quality Control Chemist will initially be responsible for conducting physical property testing and wet chemistry testing, such as viscosity, pH, and TOC for water testing. The role will expand to encompass all analytical testing, including HPLC, GC, and more. The individual will prioritize daily sample testing and perform various laboratory tests on bulk formula batches and line samples of raw materials and in-process materials. Additionally, they will review compounding and laboratory records for accuracy and completeness, investigate customer complaints and OOS/OOT results, and implement corrective actions as determined by QC supervision.Responsibilities<ul><li>Perform laboratory analysis on incoming raw materials, in-process samples, and finished products according to established procedures, including wet chemistry, GC, and HPLC.</li><li>Prepare samples for chromatographic analysis and prepare standard and reagent solutions.</li><li>Coordinate information flow within the laboratory and to internal customers.</li><li>Access, input, and retrieve information from the LIMS.</li><li>Dispose of raw materials, process samples, and finished products for use or sale.</li><li>Ensure all laboratory documentation meets standards for completeness and accuracy according to Good Documentation Practices (GDP) and GMP.</li><li>Handle laboratory clean-up and housekeeping duties, including waste disposal and glassware washing.</li><li>Document deviations in performance not anticipated or indicated in test procedures.</li><li>Become proficient in performing routine GC and HPLC analysis, including integration and result calculations.</li><li>Assist with OOS/OOT and customer complaint investigations.</li><li>Assist with method development protocols and conduct requisite testing.</li><li>Assist with IQ/OQ/PQ and instrument validation/calibration tasks.</li><li>Assist with method transfer protocols and requisite testing.</li><li>Assist with annual/new supplier validations protocol, sample transfer, and testing process.</li><li>Assist with SOP creation, review, and revision activities.</li><li>Assist with stability protocol and testing processes.</li><li>Assist with supplies/services ordering process.</li><li>Assist with contract manufacturing protocol and workflow.</li><li>Assist with instrument maintenance and troubleshooting.</li></ul>Essential Skills<ul><li>Strong multi-tasking ability and capability to prioritize or re-prioritize based on changing needs.</li><li>Effective communication skills with compounding (manufacturing) leadership.</li><li>Confidence to work independently without constant supervision.</li><li>Willingness to learn and adapt.</li><li>Ability to work in a high throughput environment within a team dynamic.</li><li>Proficiency in performing repetitive testing quickly and accurately.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's Degree minimum required, Chemistry preferred but open to Biochemistry, Biology with a Chemistry Minor, or other related science.</li><li>Strong preference for 1 year of experience in a QC laboratory with exposure to physical testing, volumetric solution sample preparation, GMP/GDP, and LIMS or other lab sample management systems.</li><li>Entry-level candidates with strong demonstrated chemistry skills will be considered.</li><li>General experience working within MS Office, including Word, Excel, Teams, Outlook, etc.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $24.00 - $24.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Aug 5, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Description-Perform qualitative and quantitative testing of samples as requested using analytical instrumentation such as HPLC, GC, UV/Vis, KF, FTIR, and various wet chemistry techniques.-Ensure that the analytical data generated is accurate, precise, and in compliance with cGMP, FDA, and company requirements.-Document testing, observations, deviations, and Out of Specification (OOS) results clearly and completely. Perform peer review of data as needed.-Coordinate and prepare samples for shipment to external testing laboratories as needed.-Demonstrate the ability to understand and follow GMPs, SOPs, and analytical procedures (compendial and in-house).-Work collaboratively in a team environment to develop and maintain a positive culture within the organization.-Maintain good housekeeping practices in the laboratory and other workspaces.-Observe and comply with company Health and Safety policies.-Contribute to a continuous improvement environment and work with management to implement agreed-upon changes.-Perform other duties as assigned.Additional Skills &amp; Qualifications· Knowledge and hands on experience with some of the following: chromatography, spectroscopy, wet chemistry and dissolution testing.· Ability to manage multiple projects simultaneously· Ability to learn and adapt to demands in a fast paced work environment· Strong written, verbal and interpersonal skills· Ability to work in a hands-on collaborative fashion with many different disciplines both inside and outside of the company· Ability to demonstrate good laboratory technique and a high degree of accuracy in the execution of different analytical techniques.Education and Experience:· B.S. degree in Chemistry, Biology, Biochemistry, or other related discipline or equivalent, directly related job experience is required.· Minimum 2 years of experience in a QC laboratory under a GMP environment is desired.· Experience with chromatographic data acquisition software is a plus.Job Type &amp; LocationThis is a Contract position based out of Mason, OH.Pay and BenefitsThe pay range for this position is $33.65 - $43.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Mason,OH.Application DeadlineThis position is anticipated to close on Aug 4, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Inspector - Job DescriptionThe Quality Control Inspector performs detailed incoming inspection of vendor-supplied components to ensure all materials meet engineering drawing specifications, dimensional tolerances, and quality standards. This highly hands-on role supports a low-volume, high-precision manufacturing environment for advanced semiconductor-related capital equipment and plays a critical part in production readiness and overall product quality.Responsibilities<ul><li>Perform incoming inspection of vendor-supplied components, including precision-machined parts, sheet metal components, system housings, and structural assemblies.</li><li>Review and validate first article inspection (FAI) documentation packages, including material certifications, vendor-provided dimensional reports, and compliance to engineering drawings.</li><li>Conduct follow-up inspections on subsequent material receipts to ensure consistency and ongoing quality compliance.</li><li>Interpret and analyze engineering drawings, specifications, and Geometric Dimensioning and Tolerancing (GD&amp;T) requirements to identify and prioritize critical-to-quality dimensions.</li><li>Perform detailed dimensional inspections using Coordinate Measuring Machines (CMM) and manual tools such as calipers, gauges, and micrometers.</li><li>Verify that all inspected features meet defined tolerances before releasing materials to production.</li><li>Set up and operate CMM equipment for precision measurement, including defining reference datums and alignment points, configuring part orientation and measurement paths, and executing inspection routines.</li><li>Adjust and optimize CMM inspection setups for new or unfamiliar part geometries to ensure accurate and repeatable measurements.</li><li>Identify non-conforming material and initiate corrective workflows in accordance with established quality procedures.</li><li>Create detailed discrepancy records within SAP, including clear descriptions of deviations, supporting inspection data, and photographic documentation when applicable.</li><li>Collaborate closely with Manufacturing Engineering to support disposition decisions such as use-as-is, vendor returns, scrap, or rework actions.</li><li>Work with Supply Chain and Buyers to communicate with vendors regarding non-conformances and corrective actions.</li><li>Serve as a key interface between incoming inspection, Manufacturing Engineering, and Supply Chain to support timely and effective resolution of quality issues.</li><li>Provide feedback to engineering teams on drawing clarity and manufacturability when inspection issues or recurring deviations arise.</li><li>Support a major production ramp by maintaining a consistent inspection workload and ensuring that components are ready for downstream manufacturing.</li><li>Exercise ownership and autonomy in making quality-related decisions that directly influence production readiness and product performance.</li></ul>Essential Skills<ul><li>High school diploma.</li><li>At least 4 years of experience in quality control, quality inspection, or quality assurance roles.</li><li>Strong hands-on experience with Coordinate Measuring Machines (CMM), including setup and operation for precision measurement.</li><li>Proficiency in performing CMM inspection and using CMM software to define datums, alignments, and measurement paths.</li><li>Experience working in ISO-based quality environments.</li><li>Experience in a machine shop or precision manufacturing environment.</li><li>Hands-on dimensional inspection experience using manual measurement tools such as calipers, gauges, micrometers, and related metrology equipment.</li><li>Ability to read and interpret engineering drawings and apply GD&amp;T (Geometric Dimensioning and Tolerancing) principles.</li><li>Familiarity with SAP or similar enterprise systems for recording discrepancies and managing quality data.</li><li>Experience with semiconductor, capital equipment, or closely related high-precision industries.</li><li>Strong attention to detail and accuracy in measurements, documentation, and inspection records.</li><li>Ability to work effectively in a fast-paced, inspection-focused environment while maintaining high quality standar</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Somerset, NJ.Pay and BenefitsThe pay range for this position is $51000.00 - $66000.00/yr.Medical, Dental, and Vision
Employee Stock Purchase Plan (ESPP)
401(k) with Company Match
Holiday, Vacation, and Sick Time
Flexible Spending Accounts (FSA)
Commuter Benefits
Life and Accident Insurance
Disability Insurance
Tuition Reimbursement
Employee Assistance Program (EAP)
Identity Theft Remediation
Emergency Travel AssistanceWorkplace TypeThis is a fully onsite position in Somerset,NJ.Application DeadlineThis position is anticipated to close on Jul 27, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Inspector

The Quality Control Inspector plays a key role in ensuring product quality and compliance by performing inspections and testing on-site for finished goods, in-process materials, and raw materials. This position coordinates external laboratory testing, reviews production and filling records for accuracy and legibility in line with current good manufacturing practices (GMP), performs swabbing for cleaning and sanitization verification, and confirms that all production activities in weighing, compounding, and filling meet established standards. The Quality Control Inspector regularly reports project and quality status updates to site leadership and supports continuous improvement of quality processes.Responsibilities<ul><li>Perform all assigned Quality Control inspection activities, including in-process and final QC inspections, work-in-progress (WIP) inspections, packaging inspections, and raw material inspections in accordance with established procedures.</li><li>Conduct first article inspections and line clearance inspections on packaging lines to ensure equipment and materials are properly set up and ready for production.</li><li>Perform pre-weigh line clearance inspections prior to compounding and batching to verify that the work area is clean, organized, and free of previous product or materials.</li><li>Inspect compounding and filling equipment for proper cleaning and sanitization, ensuring compliance with established cleaning procedures and standards.</li><li>Maintain retained finished goods, bulk, and raw material sample storage, including organizing samples and accurately updating associated logbooks.</li><li>Coordinate and arrange finished product microbiological and other specialized testing with external laboratories, ensuring samples and documentation are complete and accurate.</li><li>Collect product and material samples for testing, manage their storage and distribution, and ensure prompt and accurate shipping of samples to customers and external laboratories.</li><li>Perform scale verification checks during first article release to confirm measurement accuracy prior to production runs.</li><li>Initiate and lead non-conformance reports, support investigative work, and assist in identifying root causes and corrective actions for quality issues.</li><li>Perform laboratory testing on bulk and finished products as required, following established test methods and documenting results accurately.</li><li>Manage storage and cataloging of hardcopy batch records and packaging records, ensuring documentation is complete, organized, and easily retrievable.</li><li>Conduct and document environmental bioburden testing, particle testing, and cleaning validations for compounding and packaging equipment, ensuring compliance with internal and regulatory requirements.</li><li>Provide backup support for incoming inspection of component packaging and raw materials, including testing and documentation as needed.</li><li>Conduct training as needed on quality control procedures, inspection methods, and related topics to support team competency and compliance.</li><li>Support all safety initiatives at the site by following safety procedures, identifying potential hazards, and promoting a safe work environment.</li><li>Assist with administrative tasks such as filing, organizing, and maintaining documentation relevant to Quality Control inspection activities.</li><li>Work under minimal supervision while managing assigned tasks, meeting deadlines, and maintaining high quality standards.</li><li>Collaborate and communicate effectively with production, quality, and other cross-functional teams to resolve issues and support smooth operations.</li></ul>Essential Skills<ul><li>High school diploma or equivalent.</li><li>Basic computer skills, including the ability to use Word and Excel.</li><li>At least 1 year of experience working with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).</li><li>At least 1 year of experience in a manufacturing environment, preferably in a quality-related role.</li><li>Strong attention to detail and good organizational skills to manage samples, records, and inspection activities.</li><li>Good communication and interaction skills to work effectively with cross-functional teams.</li><li>Ability to follow written work instructions and standard operating procedures accurately.</li><li>Ability to work under minimal supervision while maintaining high standards of quality and compliance.</li><li>Flexibility to work overtime and weekends as scheduled to support production and quality needs.</li><li>Problem-solving and decision-making skills to identify issues, evaluate options, and support corrective actions.</li><li>Ability to speak, read, and write English clearly and accurately.</li><li>Ability to properly use standard inspection equipment such as calipers, thickness gauges, and other measurement gauges.</li><li>Demonstrated ability to read, understand, and apply information contained in technical documentation, procedures, and drawings, including basic geometric tolerances.</li><li>Capability to perform job-related tasks associated with using mechanical and/or electrical pallet jacks to move pallets and skids, with appropriate documented training.</li></ul>Additional Skills &amp; Qualifications<ul><li>Technical degree is a plus and can enhance understanding of manufacturing and quality processes.</li><li>ASQ (American Society for Quality) Quality Certification is a plus and demonstrates a strong foundation in quality principles and practices.</li><li>Bilingual skills are a plus and can support effective communication in a diverse workforce.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Dallas, TX.Pay and BenefitsThe pay range for this position is $21.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Dallas,TX.Application DeadlineThis position is anticipated to close on Aug 4, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Inspector/Specialist

QC Lab Analyst3rd shift 4-10s (M-Thur)Job DescriptionThis role focuses on performing routine and project-based qPCR testing to support in-process and finished product quality control in a GMP pharmaceutical environment. The Quality Control Analyst conducts time-sensitive qPCR assays, handles raw material and finished product samples, supports method validation and development, and contributes to environmental and contaminant monitoring in a brand-new laboratory operating around the clock.Responsibilities<ul><li>Perform routine qPCR testing on samples with a 7-hour turnaround time, working in parallel with another analyst to ensure timely completion.</li><li>Conduct in-process testing on raw materials, primarily pig-origin tissue slurries, including extraction of RNA from tissue samples.</li><li>Perform finished product testing on final drug product and select specialty products, including some testing for additional sites.</li><li>Run speciation assays to identify and quantify different species within a sample.</li><li>Carry out contaminant monitoring and positive control environmental monitoring while samples are running.</li><li>Perform calibration and routine maintenance of laboratory instruments, including centrifuges, spectrophotometers, and liquid handler robots.</li><li>Prepare reagents, manage inventory, and ensure that all necessary materials are available and properly documented.</li><li>Support validation activities, including validating basic centrifuges, spectrophotometers, liquid handler robots, laboratory software, and lab spaces.</li><li>Assist with software programming related to qPCR and laboratory instruments as part of validation and method support.</li><li>Draft and support laboratory methods, including method development and documentation in accordance with GMP and FDA expectations.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associates or Bachelor’s degree in Microbiology or a related discipline preferred for all levels.</li><li>High School Diploma or G.E.D. required for all levels.</li><li>Minimum of 1 year of working in a regulated laboratory environment.</li><li>Experience with pipettes required.</li><li>PCR experience from school or industry is preferred but not required.</li><li>Open to different experience levels: Associate, Analyst, and Sr</li></ul>Work EnvironmentThe role is on third shift, Monday through Thursday, working 10-hour days starting at 9:00 p.m. Job Type &amp; LocationThis is a Permanent position based out of Madison, WI.Pay and BenefitsThe pay range for this position is $45760.00 - $75000.00/yr.Competitive compensation; excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&amp;D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; 401kWorkplace TypeThis is a fully onsite position in Madison,WI.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Lab Analyst

Become the gatekeeper of product quality. Use your chemistry or chemical engineeringto perform critical testing, support production, and make real-time quality decisions that impact manufacturing success.Job Title: 1st Shift Quality Control Lab TechnicianJob DescriptionThe Quality Control Lab Technician supports a fast-paced manufacturing environment by performing accurate and timely quality testing on raw materials, bulk batches, and finished products. This role ensures that all materials meet specifications, communicates clearly with production operators on test results and batch adjustments, and initiates investigations into non-conforming materials. The position offers the opportunity to streamline testing processes, contribute to continuous improvement, and grow into higher-responsibility roles over time.Responsibilities<ul><li>Perform timely and accurate chemical, physical, and visual testing on raw materials, bulk batches, and finished goods using standard test procedures.</li><li>Determine appropriate raw material adjustment amounts for bulk batches to ensure products meet required specifications.</li><li>Enter test results for raw materials, bulk batches, and finished goods into the ERP system (SAP) accurately and promptly.</li><li>Perform timely usage decisions (accept or reject) for raw materials, bulk batches, and finished goods in SAP based on test results and specifications.</li><li>Collect, label, and store retain samples of raw materials, bulk batches, and finished products as required for traceability and investigations.</li><li>Take immediate action on internal non-conformances by creating notifications in SAP and performing initial investigations in collaboration with operators.</li><li>Support customer complaint investigations by reviewing batch records, analyzing retain samples, and providing clear documentation of findings.</li><li>Maintain critical laboratory equipment, instruments, and inventory of supplies to support continuous and uninterrupted quality control testing.</li><li>Review the daily production schedule and ensure test equipment, reagents, and materials are prepared to efficiently test all scheduled batches.</li><li>Provide clear documentation and visual quality control labels for materials and products that are acceptable, rejected, or on hold.</li><li>Issue, complete, maintain, and process all relevant quality control paperwork and records in an organized and compliant manner.</li><li>Participate in and support audits, including ISO and other quality system audits, by providing documentation and explaining lab processes.</li><li>Contribute to root cause and corrective action activities by helping identify issues, analyzing data, and updating documentation as needed.</li><li>Attend monthly meetings focused on quality, safety, housekeeping, and waste minimization, and actively contribute ideas for improvement.</li><li>Communicate all critical issues and problems related to quality control test equipment, test delays, or potential quality risks promptly to management.</li><li>Collaborate closely with production operators and other team members to ensure clear, proactive cross-communication and timely issue resolution.</li><li>Act as a team player by volunteering to help where needed, supporting colleagues, and contributing to a positive and collaborative work environment.</li><li>Help streamline the testing process by identifying opportunities to reduce duplication of effort and improve efficiency within the lab.</li><li>Participate in lean manufacturing and continuous improvement activities, applying principles such as Six Sigma where appropriate.</li><li>Handle production-related quality control tasks with urgency and accountability, recognizing the lab’s role as the gatekeeper of production quality.</li></ul>Essential Skills<ul><li>Bachelor of Science degree in Chemical Engineering or Chemistry.</li><li>Minimum of 1+ years of experience in a quality control, laboratory, manufacturing, or operations environment, ideally involving cross-functional communication.</li><li>Experience performing chemical, physical, and visual testing in a lab setting using standard test procedures.</li><li>Proficiency with ERP systems, specifically SAP, for entering test results and making usage decisions.</li><li>Strong communication skills with the ability to communicate promptly, clearly, and proactively with operators, peers, and management.</li><li>High attention to detail and accuracy in testing, documentation, and data entry.</li><li>Experience participating in audits, preferably within an ISO or similar quality management environment.</li><li>Exposure to root cause analysis and corrective action processes, including updating documentation and records.</li><li>Familiarity with Microsoft Excel, Microsoft Teams, and Outlook for data handling, collaboration, and communication.</li><li>Ability to manage multiple tasks and priorities in a fast-paced lab environment while meeting production schedules.</li><li>Demonstrated commitment to safety, including adherence to EHS requirements, safe work practices, and proper use of personal protective equipment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in aerospace, manufacturing, or consumer products industries.</li><li>Experience working in or around adhesives, chemicals, or similar industrial materials.</li><li>Prior involvement in continuous improvement initiatives focused on process efficiency and waste reduction.</li><li>Strong project and time management skills, with the ability to plan testing around production schedules.</li><li>Comfort working as a key quality gatekeeper, making timely decisions that directly impact production flow.</li><li>Motivated, growth-oriented mindset with a desire to take on increasing responsibility and potentially advance into higher-level technical or leadership roles over time.</li><li>Flexibility and openness to learning new processes, equipment, and systems as the lab and facility evolve.</li><li>Willingness to consider long-term growth opportunities, including potential relocation to another facility in the future.</li></ul>Work EnvironmentThis is a first-shift position, typically scheduled from 8:00 a.m. to 4:30 p.m., working in a laboratory setting within a manufacturing facility. The environment involves hands-on work with adhesives and related materials, and the lab and facility may have a strong, noticeable smell associated with these products. Candidates should be comfortable working in this type of sensory environment and will be made aware of these conditions during onsite interviews. The role requires consistent use of appropriate personal protective equipment and adherence to all environmental, health, and safety requirements. The lab supports a production operation in aerospace, manufacturing, and consumer products, so work is often time-sensitive and closely tied to production schedules. The culture emphasizes teamwork, proactive communication, continuous improvement, and professional growth, offering opportunities for long-term development for individuals who are eager to learn and advance.Job Type &amp; LocationThis is a Contract to Hire position based out of Los Angeles, CA.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Los Angeles,CA.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Lab Tech

Job Title: Quality Control Laboratory Technician / Microbiologist Technician Job DescriptionThis role supports the Sample Collection Division as a Quality Control Laboratory Technician with a focus on microbiology. You will perform microbiological testing on raw materials, finished products, and environmental samples, ensuring compliance with quality standards and regulatory requirements. The position offers the opportunity to contribute to pharmaceutical, nutritional, and animal health projects while working closely with a collaborative laboratory and quality team.Responsibilities<ul><li>Perform microbiological testing of raw materials, finished products, and environmental monitoring samples using established laboratory methods and aseptic techniques.</li><li>Ensure strict compliance with standard operating procedures (SOPs), Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), and applicable regulatory requirements.</li><li>Support investigations into microbial deviations by participating in root cause analyses and implementing corrective and preventive actions.</li><li>Monitor, troubleshoot, calibrate, validate, and maintain laboratory equipment to ensure accurate and reliable test results.</li><li>Maintain accurate and complete laboratory records, including laboratory notebooks, data archives, retention samples, and change control documentation.</li><li>Compile, review, and analyze laboratory data to support quality trending programs and continuous improvement initiatives.</li><li>Assist with internal and external quality audits, document control activities, and other Quality Assurance responsibilities.</li><li>Support stability studies and product testing, including preparation of media, samples, and documentation as required.</li><li>Conduct inspection and analysis of samples in accordance with ISO standards, ISO procedures, and GMP guidelines.</li><li>Order and manage laboratory supplies to ensure adequate inventory and support uninterrupted laboratory operations.</li><li>Maintain a clean, safe, and organized laboratory environment, including proper handling and disposal of media, reagents, and samples.</li><li>Follow all safety procedures, laboratory protocols, and company policies to promote a safe and compliant work environment.</li><li>Collaborate with cross-functional teams to support laboratory, biology, and environmental monitoring activities and contribute to overall quality system improvements.</li></ul>Essential Skills<ul><li>At least 1 year of microbiology, laboratory, or quality control experience, preferably in a laboratory setting.</li><li>Bachelor's degree in Microbiology, Biology, Life Sciences, or a related field preferred.</li><li>Hands-on experience with microbiology testing and laboratory techniques, including aseptic technique, environmental monitoring, and microbial testing.</li><li>Knowledge of quality control and quality assurance principles, including GLP, cGMP, SOP compliance, and audit support.</li><li>Strong documentation and record-keeping skills, including maintaining laboratory notebooks, investigations, change control, and data management.</li><li>Experience with root cause investigation and troubleshooting for deviations, equipment issues, and method-related problems.</li><li>Ability to monitor, calibrate, qualify, validate, and perform preventive maintenance on laboratory equipment.</li><li>Working knowledge of quality systems, ISO standards, ISO procedures, and GMP requirements.</li><li>Strong attention to detail and accuracy in testing, documentation, and data analysis.</li><li>Effective written and verbal communication skills and the ability to work collaboratively in a team environment.</li><li>Demonstrated investigative and problem-solving abilities in a regulated or structured laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a regulated laboratory environment, including GLP and cGMP settings, is a plus.</li><li>Background in microbiology laboratories, including handling media, environmental monitoring, and microbial analysis.</li><li>Familiarity with quality assurance activities such as audits, document control, and quality trending programs.</li><li>Exposure to stability studies, product testing, and continuous improvement initiatives.</li><li>Experience working with raw materials inspection, analysis, and adherence to ISO standards and procedures.</li><li>Ability to manage multiple tasks in a fast-paced laboratory environment while maintaining high quality standards.</li><li>Comfort working on projects related to pharmaceuticals, nutritional products, veterinary instruments, diagnostics, and agricultural chemicals.</li><li>Interest in animal health, including products that support livestock, companion animals, and racehorses.</li></ul>Work EnvironmentThe role is based in a laboratory environment within a global animal safety and health-focused facility. The site manufactures and distributes veterinary instruments, diagnostics, pharmaceuticals, nutritional supplements, disinfectants, and agricultural chemicals that protect the health of livestock, companion animals, and racehorses. The laboratory operates under GLP, cGMP, ISO standards, and established SOPs, with a strong emphasis on safety, cleanliness, and organization. You will work with microbiology laboratories, environmental monitoring systems, aseptic techniques, and a variety of analytical equipment that requires regular calibration, qualification, and validation. The organization has recently restructured and operates under new leadership, offering the opportunity to join a growing team engaged in exciting pharmaceutical and nutritional projects across multiple industries. The culture emphasizes collaboration, continuous improvement, and adherence to quality and safety procedures in a professional, team-oriented setting.Job Type &amp; LocationThis is a Contract to Hire position based out of Lexington, KY.Pay and BenefitsThe pay range for this position is $22.06 - $22.06/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Lexington,KY.Application DeadlineThis position is anticipated to close on Jul 29, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Laboratory Technician

<h2>Job Title: Quality Control Laboratory Technician</h2>Leading manufacturer in adhesives, sealants, and polymers is looking for a QC laboratory technician to join their team! Opportunity to gain experience in a manufacturing environment!*BS in Chemistry or related field is required*Essential Skills<ul><li>Minimum of 1+ years of experience in a quality control, laboratory, or related operations environment, with strong cross-functional communication</li><li>Experience performing chemical, physical, and visual testing in a laboratory or production setting.</li><li>Ability to interpret test results and determine appropriate batch or raw material adjustments to meet specifications.</li><li>Strong attention to detail and a high level of accuracy in testing, documentation, and data entry.</li><li>Experience using ERP systems, preferably SAP, for entering test results, making usage decisions, and creating notifications.</li><li>Willingness to follow safety procedures, wear appropriate PPE, and work in an environment with strong odors associated with adhesives.</li></ul>Job DescriptionThe Quality Control Laboratory Technician supports the manufacturing process by performing accurate and timely quality testing on raw materials, bulk batches, and finished products. This role ensures that all materials meet specifications, communicates test results and required batch adjustments to production operators, and initiates investigations for non-conforming materials. The technician plays a critical role as a gatekeeper for production quality, helping streamline testing processes and supporting continuous improvement within the facility.Responsibilities<ul><li>Execute and adhere to all Environmental, Health, and Safety (EHS) requirements, maintain a safe work environment, and follow internal safety rules and procedures, including wearing appropriate personal protective equipment (PPE).</li><li>Participate in general housekeeping of the plant and laboratory areas to maintain a clean, organized, and safe workspace.</li><li>Comply with all company policies, procedures, and quality standards.</li><li>Perform timely and accurate chemical, physical, and visual testing on raw materials, bulk batches, and finished goods using standard test procedures.</li><li>Determine appropriate raw material adjustment amounts for bulk batches to ensure products meet required specifications.</li><li>Enter raw material, bulk batch, and finished goods test results into the ERP system (SAP) accurately and promptly.</li><li>Perform timely usage decisions (accept or reject) for raw materials, bulk batches, and finished goods in SAP.</li><li>Collect and store retain samples of raw materials, bulk batches, and finished products as required for traceability and future reference.</li><li>Take immediate action on internal non-conformances by creating notifications in SAP and conducting initial investigations with operators.</li><li>Support customer complaint investigations by reviewing batch records and examining retain samples to help identify root causes.</li><li>Maintain critical laboratory equipment and inventory of supplies to ensure continuous, uninterrupted quality control support.</li><li>Review the daily production schedule and ensure test equipment, reagents, and materials are prepared to efficiently test all scheduled batches.</li><li>Provide clear documentation and visual quality control labels for materials and products that are acceptable, rejected, or on hold.</li><li>Issue, complete, maintain, and process all relevant paperwork and records related to quality control activities.</li><li>Attend monthly meetings focused on quality, safety, housekeeping, and waste minimization, and contribute to ongoing improvement initiatives.</li><li>Communicate all critical issues and problems related to quality control test equipment and potential testing delays to management in a timely manner.</li><li>Collaborate as a team player, volunteering to help where needed to complete work and enhance skills.</li><li>Work under the guidance and direction of laboratory staff and facility technical leadership while developing greater independence over time.</li><li>Help streamline the testing process by identifying and implementing more efficient ways of working, reducing duplication of effort among team members.</li></ul>Work EnvironmentThis role is based in a laboratory setting within a manufacturing facility that produces adhesive products. The environment involves working closely with production operations and requires strong project and time management skills to support a dynamic production schedule. The lab and facility have a strong adhesive-related smell, and candidates should be comfortable working in an area with noticeable odors; this will be made clear and visible during onsite interviews. The position involves regular use of laboratory test equipment, reagents, and an ERP system (SAP), along with common office technologies such as Excel, Teams, and Outlook. Personal protective equipment (PPE) is required, and adherence to safety procedures is essential. The work culture emphasizes teamwork, proactive communication, housekeeping, safety, quality, and continuous improvement, with opportunities for long-term growth for individuals who are open to expanding their responsibilities and potentially relocating in the future.Job Type &amp; LocationThis is a Contract to Hire position based out of Los Angeles, CA.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Los Angeles,CA.Application DeadlineThis position is anticipated to close on Jul 29, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Lab TechnicianJob DescriptionThe Quality Control Lab Technician will be responsible for ensuring that all production batches and finished products meet the necessary quality control standards. This role involves conducting tests in accordance with internal Standard Operating Procedures (SOPs) and FDA/GMP requirements. The technician will perform routine quality control activities, record observations and measurements, and report results. Additional responsibilities include cleaning, disinfecting, and maintaining glassware and equipment, as well as assisting with the receipt and inspection of raw materials.Responsibilities<ul><li>Test and adjust production batches as required by formula and SOP; communicate and record adjustments.</li><li>Test finished products, stability, and validation samples using required methods.</li><li>Perform instrumental analyses using HPLC, GC, or TOC as needed.</li><li>Complete all paperwork, record keeping, and posting associated with approving and releasing batches.</li><li>Evaluate data for trends and author standard operating procedures and microbiological test methods.</li><li>Approve tankers for loading and unloading; record information and testing results.</li><li>Test products based on customer complaints or returns and retest returned goods for release or rejection as authorized.</li><li>Store samples as required and assist in maintaining retained samples.</li><li>Maintain cleanliness and stock the QC area and lab with necessary materials.</li><li>Assist in environmental monitoring, including obtaining samples and conducting chemical or micro evaluations.</li><li>Operate computer programs for administrative duties to prepare, distribute, and maintain forms, charts, logs, graphs, and other written tools.</li><li>Assist in the company’s compliance with current Good Manufacturing Practices.</li><li>Communicate with other shifts regarding special microbiological testing and pertinent issues.</li><li>Perform other duties as required or assigned, including special analytical projects and validations.</li></ul>Essential Skills<ul><li>Proficiency in chemistry and laboratory work.</li><li>Experience in QC lab work, including wet chemistry and titration.</li><li>Knowledge of inspection, biology, biochemistry, and wet laboratory practices.</li><li>Skill in pH testing and gas chromatography.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor of Science degree in chemistry or a related science field.</li><li>Working knowledge of various testing apparatus, including HPLC and GC.</li><li>Familiarity with basic lab equipment in a manufacturing setting.</li></ul>Work EnvironmentThe role operates on the 3rd shift from 10:30 PM to 6:30 AM, Sunday through Friday morning, with occasional Saturday work based on production needs. The company offers a family-owned, small team atmosphere that promotes close collaboration, extensive training, and one-on-one mentorship. The work environment emphasizes consistent values, meaningful work, great communication, and job security in a thriving industry.Job Type &amp; LocationThis is a Contract to Hire position based out of Sharonville, OH.Pay and BenefitsThe pay range for this position is $23.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Sharonville,OH.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2 style="text-align:center;"> Quality Control Laboratory Technician</h2>Job DescriptionThe Quality Control Laboratory Technician ensures that all finished products meet established quality and safety standards by performing laboratory testing, analyzing raw materials and finished goods, and supporting quality assurance processes in a food processing and ingredients manufacturing environment.Responsibilities<ul><li>Perform quality control testing on raw materials, in-process samples, and finished products to ensure they meet established specifications and regulatory requirements.</li><li>Conduct laboratory analyses using wet chemistry, microbiology, and other analytical techniques to evaluate product quality and safety.</li><li>Measure and monitor viscosity and other physical and chemical properties of products and raw materials.</li><li>Operate, calibrate, and maintain quality control analysis equipment and laboratory instruments according to standard procedures.</li><li>Document test results accurately and promptly using computer systems and data processing tools, ensuring complete and traceable records.</li><li>Assist in quality assurance and GMP-related activities by following established procedures and supporting compliance with FDA and other applicable regulations.</li><li>Identify and report non-conformances, deviations, or unusual test results to the appropriate personnel for investigation and corrective action.</li><li>Follow Good Manufacturing Practices (GMP) and laboratory safety protocols to maintain a clean, safe, and compliant work area.</li><li>Collaborate with production and quality teams to support continuous improvement of processes and product quality.</li><li>Climb ladders to access work platforms and sampling points as needed and handle materials and equipment safely, including lifting up to 50 pounds.</li><li>Participate in training and shift transitions to ensure consistent testing practices and effective communication across shifts.</li></ul>Essential Skills<ul><li>High school diploma or GED with 1–2 years of related work experience in a laboratory, quality control, or similar environment.</li><li>Ability to use quality control analysis equipment and laboratory instruments effectively and safely.</li><li>Fluency in spoken and written English to read procedures, document results, and communicate with team members.</li><li>Strong mathematical skills to perform calculations, interpret numerical data, and evaluate test results.</li><li>Computer and data processing skills to enter, manage, and analyze laboratory and quality data.</li><li>Ability to climb ladders to reach work platforms and sampling locations.</li><li>Ability to lift up to 50 pounds safely as part of routine job duties.</li><li>Knowledge of or experience with food science, chemistry, microbiology, biology, and wet chemistry techniques.</li><li>Understanding of quality control and quality assurance principles in a manufacturing or laboratory setting.</li><li>Familiarity with FDA regulations and Good Manufacturing Practices (GMP) in a food-related environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate or bachelor’s degree in food science, chemistry, biology, or a related scientific discipline is preferred.</li><li>Experience working in a food processing or food ingredients manufacturing environment.</li><li>Hands-on experience with viscosity measurement and raw materials testing.</li><li>Experience in laboratory analysis related to food science, microbiology, chemistry, or biology.</li><li>Attention to detail and strong organizational skills to manage multiple tests and samples.</li><li>Ability to work effectively across different shifts and adapt to changing production and testing priorities.</li><li>Willingness to work occasional overtime, including 12-hour shifts when required with prior notification.</li></ul>Work EnvironmentThis role operates within a quality assurance testing laboratory that supports a food processing and food ingredients manufacturing facility. You will work with laboratory equipment and quality control analysis instruments to test raw materials, in-process samples, and finished products. The position requires working on multiple shifts: initial training takes place on 1st shift (6:00 a.m.–2:00 p.m.), followed by assignment to an open shift on either 2nd shift (2:00 p.m.–10:00 p.m., Monday–Friday) or 3rd shift (10:00 p.m.–6:00 a.m., Sunday–Thursday, with occasional Fridays as needed). Some overtime, including potential 12-hour shifts, may be required with prior notification. The environment emphasizes Good Manufacturing Practices (GMP), regulatory compliance, and safety, with regular movement around the facility, climbing ladders to work platforms, and lifting up to 50 pounds as part of routine tasks.Job Type &amp; LocationThis is a Contract to Hire position based out of Horn Lake, MS.Pay and BenefitsThe pay range for this position is $22.00 - $27.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Horn Lake,MS.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2>Quality Control Lab Technician</h2>INTERESTED CANDIDATES PLEASE REACH OUT TO CARRIE AT CSTUDEBA @ACTALENTSERVICES.COM OR TEXT 937. 903. 3402 TO SET UP A PHONE INTERVIEW!Actalent is seeking a Quality Control Lab Technician to be be responsible for ensuring that all production batches and finished products meet the necessary quality control standards. This role involves conducting tests in accordance with internal Standard Operating Procedures (SOPs) and FDA/GMP requirements. The technician will perform routine quality control activities, record observations and measurements, and report results. Additional responsibilities include cleaning, disinfecting, and maintaining glassware and equipment, as well as assisting with the receipt and inspection of raw materials.Responsibilities<ul><li>Test and adjust production batches as required by formula and SOP; communicate and record adjustments.</li><li>Test finished products, stability, and validation samples using required methods.</li><li>Perform instrumental analyses using HPLC, GC, or TOC as needed.</li><li>Complete all paperwork, record keeping, and posting associated with approving and releasing batches.</li><li>Evaluate data for trends and author standard operating procedures and microbiological test methods.</li><li>Approve tankers for loading and unloading; record information and testing results.</li><li>Test products based on customer complaints or returns and retest returned goods for release or rejection as authorized.</li><li>Store samples as required and assist in maintaining retained samples.</li><li>Maintain cleanliness and stock the QC area and lab with necessary materials.</li><li>Assist in environmental monitoring, including obtaining samples and conducting chemical or micro evaluations.</li><li>Operate computer programs for administrative duties to prepare, distribute, and maintain forms, charts, logs, graphs, and other written tools.</li><li>Assist in the company’s compliance with current Good Manufacturing Practices.</li><li>Communicate with other shifts regarding special microbiological testing and pertinent issues.</li><li>Perform other duties as required or assigned, including special analytical projects and validations.</li></ul>Essential Skills<ul><li>Proficiency in chemistry and laboratory work.</li><li>Experience in QC lab work, including wet chemistry and titration.</li><li>Knowledge of inspection, biology, biochemistry, and wet laboratory practices.</li><li>Skill in pH testing and gas chromatography.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor of Science degree in chemistry or a related science field.</li><li>Working knowledge of various testing apparatus, including HPLC and GC.</li><li>Familiarity with basic lab equipment in a manufacturing setting.</li></ul>Work EnvironmentThe role operates on the 3rd shift from 10:30 PM to 6:30 AM, Sunday through Friday morning, with occasional Saturday work based on production needs. The company offers a family-owned, small team atmosphere that promotes close collaboration, extensive training, and one-on-one mentorship. The work environment emphasizes consistent values, meaningful work, great communication, and job security in a thriving industry.Job Type &amp; LocationThis is a Contract to Hire position based out of Sharonville, OH.Pay and BenefitsThe pay range for this position is $23.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Sharonville,OH.Application DeadlineThis position is anticipated to close on Aug 3, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2 style="text-align:center;"> Quality Control Laboratory Technician</h2>Job DescriptionThe Quality Control Laboratory Technician ensures that all finished products meet established quality and safety standards by performing laboratory testing, analyzing raw materials and finished goods, and supporting quality assurance processes in a food processing and ingredients manufacturing environment.Responsibilities<ul><li>Perform quality control testing on raw materials, in-process samples, and finished products to ensure they meet established specifications and regulatory requirements.</li><li>Conduct laboratory analyses using wet chemistry, microbiology, and other analytical techniques to evaluate product quality and safety.</li><li>Measure and monitor viscosity and other physical and chemical properties of products and raw materials.</li><li>Operate, calibrate, and maintain quality control analysis equipment and laboratory instruments according to standard procedures.</li><li>Document test results accurately and promptly using computer systems and data processing tools, ensuring complete and traceable records.</li><li>Assist in quality assurance and GMP-related activities by following established procedures and supporting compliance with FDA and other applicable regulations.</li><li>Identify and report non-conformances, deviations, or unusual test results to the appropriate personnel for investigation and corrective action.</li><li>Follow Good Manufacturing Practices (GMP) and laboratory safety protocols to maintain a clean, safe, and compliant work area.</li><li>Collaborate with production and quality teams to support continuous improvement of processes and product quality.</li><li>Climb ladders to access work platforms and sampling points as needed and handle materials and equipment safely, including lifting up to 50 pounds.</li><li>Participate in training and shift transitions to ensure consistent testing practices and effective communication across shifts.</li></ul>Essential Skills<ul><li>High school diploma or GED with 1–2 years of related work experience in a laboratory, quality control, or similar environment.</li><li>Ability to use quality control analysis equipment and laboratory instruments effectively and safely.</li><li>Fluency in spoken and written English to read procedures, document results, and communicate with team members.</li><li>Strong mathematical skills to perform calculations, interpret numerical data, and evaluate test results.</li><li>Computer and data processing skills to enter, manage, and analyze laboratory and quality data.</li><li>Ability to climb ladders to reach work platforms and sampling locations.</li><li>Ability to lift up to 50 pounds safely as part of routine job duties.</li><li>Knowledge of or experience with food science, chemistry, microbiology, biology, and wet chemistry techniques.</li><li>Understanding of quality control and quality assurance principles in a manufacturing or laboratory setting.</li><li>Familiarity with FDA regulations and Good Manufacturing Practices (GMP) in a food-related environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate or bachelor’s degree in food science, chemistry, biology, or a related scientific discipline is preferred.</li><li>Experience working in a food processing or food ingredients manufacturing environment.</li><li>Hands-on experience with viscosity measurement and raw materials testing.</li><li>Experience in laboratory analysis related to food science, microbiology, chemistry, or biology.</li><li>Attention to detail and strong organizational skills to manage multiple tests and samples.</li><li>Ability to work effectively across different shifts and adapt to changing production and testing priorities.</li><li>Willingness to work occasional overtime, including 12-hour shifts when required with prior notification.</li></ul>Work EnvironmentThis role operates within a quality assurance testing laboratory that supports a food processing and food ingredients manufacturing facility. You will work with laboratory equipment and quality control analysis instruments to test raw materials, in-process samples, and finished products. The position requires working on multiple shifts: initial training takes place on 1st shift (6:00 a.m.–2:00 p.m.), followed by assignment to an open shift on either 2nd shift (2:00 p.m.–10:00 p.m., Monday–Friday) or 3rd shift (10:00 p.m.–6:00 a.m., Sunday–Thursday, with occasional Fridays as needed). Some overtime, including potential 12-hour shifts, may be required with prior notification. The environment emphasizes Good Manufacturing Practices (GMP), regulatory compliance, and safety, with regular movement around the facility, climbing ladders to work platforms, and lifting up to 50 pounds as part of routine tasks.Job Type &amp; LocationThis is a Contract to Hire position based out of Horn Lake, MS.Pay and BenefitsThe pay range for this position is $22.00 - $27.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Horn Lake,MS.Application DeadlineThis position is anticipated to close on Jul 27, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2>Job Title: Quality Control Laboratory Technician</h2>Leading manufacturer in adhesives, sealants, and polymers is looking for a QC laboratory technician to join their team! Opportunity to gain experience in a manufacturing environment!*BS in Chemistry or related field is required*Essential Skills<ul><li>Minimum of 1+ years of experience in a quality control, laboratory, or related operations environment, with strong cross-functional communication</li><li>Experience performing chemical, physical, and visual testing in a laboratory or production setting.</li><li>Ability to interpret test results and determine appropriate batch or raw material adjustments to meet specifications.</li><li>Strong attention to detail and a high level of accuracy in testing, documentation, and data entry.</li><li>Experience using ERP systems, preferably SAP, for entering test results, making usage decisions, and creating notifications.</li><li>Willingness to follow safety procedures, wear appropriate PPE, and work in an environment with strong odors associated with adhesives.</li></ul>Job DescriptionThe Quality Control Laboratory Technician supports the manufacturing process by performing accurate and timely quality testing on raw materials, bulk batches, and finished products. This role ensures that all materials meet specifications, communicates test results and required batch adjustments to production operators, and initiates investigations for non-conforming materials. The technician plays a critical role as a gatekeeper for production quality, helping streamline testing processes and supporting continuous improvement within the facility.Responsibilities<ul><li>Execute and adhere to all Environmental, Health, and Safety (EHS) requirements, maintain a safe work environment, and follow internal safety rules and procedures, including wearing appropriate personal protective equipment (PPE).</li><li>Participate in general housekeeping of the plant and laboratory areas to maintain a clean, organized, and safe workspace.</li><li>Comply with all company policies, procedures, and quality standards.</li><li>Perform timely and accurate chemical, physical, and visual testing on raw materials, bulk batches, and finished goods using standard test procedures.</li><li>Determine appropriate raw material adjustment amounts for bulk batches to ensure products meet required specifications.</li><li>Enter raw material, bulk batch, and finished goods test results into the ERP system (SAP) accurately and promptly.</li><li>Perform timely usage decisions (accept or reject) for raw materials, bulk batches, and finished goods in SAP.</li><li>Collect and store retain samples of raw materials, bulk batches, and finished products as required for traceability and future reference.</li><li>Take immediate action on internal non-conformances by creating notifications in SAP and conducting initial investigations with operators.</li><li>Support customer complaint investigations by reviewing batch records and examining retain samples to help identify root causes.</li><li>Maintain critical laboratory equipment and inventory of supplies to ensure continuous, uninterrupted quality control support.</li><li>Review the daily production schedule and ensure test equipment, reagents, and materials are prepared to efficiently test all scheduled batches.</li><li>Provide clear documentation and visual quality control labels for materials and products that are acceptable, rejected, or on hold.</li><li>Issue, complete, maintain, and process all relevant paperwork and records related to quality control activities.</li><li>Attend monthly meetings focused on quality, safety, housekeeping, and waste minimization, and contribute to ongoing improvement initiatives.</li><li>Communicate all critical issues and problems related to quality control test equipment and potential testing delays to management in a timely manner.</li><li>Collaborate as a team player, volunteering to help where needed to complete work and enhance skills.</li><li>Work under the guidance and direction of laboratory staff and facility technical leadership while developing greater independence over time.</li><li>Help streamline the testing process by identifying and implementing more efficient ways of working, reducing duplication of effort among team members.</li></ul>Work EnvironmentThis role is based in a laboratory setting within a manufacturing facility that produces adhesive products. The environment involves working closely with production operations and requires strong project and time management skills to support a dynamic production schedule. The lab and facility have a strong adhesive-related smell, and candidates should be comfortable working in an area with noticeable odors; this will be made clear and visible during onsite interviews. The position involves regular use of laboratory test equipment, reagents, and an ERP system (SAP), along with common office technologies such as Excel, Teams, and Outlook. Personal protective equipment (PPE) is required, and adherence to safety procedures is essential. The work culture emphasizes teamwork, proactive communication, housekeeping, safety, quality, and continuous improvement, with opportunities for long-term growth for individuals who are open to expanding their responsibilities and potentially relocating in the future.Job Type &amp; LocationThis is a Contract to Hire position based out of Los Angeles, CA.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Los Angeles,CA.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control Laboratory Technician / Microbiologist TechnicianJob DescriptionThis role supports the Sample Collection Division as a Quality Control Laboratory Technician with a focus on microbiology. You will perform microbiological testing on raw materials, finished products, and environmental samples, ensuring compliance with quality standards and regulatory requirements. The position offers the opportunity to contribute to pharmaceutical, nutritional, and animal health projects while working closely with a collaborative laboratory and quality team.Responsibilities<ul><li>Perform microbiological testing of raw materials, finished products, and environmental monitoring samples using established laboratory methods and aseptic techniques.</li><li>Ensure strict compliance with standard operating procedures (SOPs), Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), and applicable regulatory requirements.</li><li>Support investigations into microbial deviations by participating in root cause analyses and implementing corrective and preventive actions.</li><li>Monitor, troubleshoot, calibrate, validate, and maintain laboratory equipment to ensure accurate and reliable test results.</li><li>Maintain accurate and complete laboratory records, including laboratory notebooks, data archives, retention samples, and change control documentation.</li><li>Compile, review, and analyze laboratory data to support quality trending programs and continuous improvement initiatives.</li><li>Assist with internal and external quality audits, document control activities, and other Quality Assurance responsibilities.</li><li>Support stability studies and product testing, including preparation of media, samples, and documentation as required.</li><li>Conduct inspection and analysis of samples in accordance with ISO standards, ISO procedures, and GMP guidelines.</li><li>Order and manage laboratory supplies to ensure adequate inventory and support uninterrupted laboratory operations.</li><li>Maintain a clean, safe, and organized laboratory environment, including proper handling and disposal of media, reagents, and samples.</li><li>Follow all safety procedures, laboratory protocols, and company policies to promote a safe and compliant work environment.</li><li>Collaborate with cross-functional teams to support laboratory, biology, and environmental monitoring activities and contribute to overall quality system improvements.</li></ul>Essential Skills<ul><li>At least 1 year of microbiology, laboratory, or quality control experience, preferably in a laboratory setting.</li><li>Bachelor's degree in Microbiology, Biology, Life Sciences, or a related field preferred.</li><li>Hands-on experience with microbiology testing and laboratory techniques, including aseptic technique, environmental monitoring, and microbial testing.</li><li>Knowledge of quality control and quality assurance principles, including GLP, cGMP, SOP compliance, and audit support.</li><li>Strong documentation and record-keeping skills, including maintaining laboratory notebooks, investigations, change control, and data management.</li><li>Experience with root cause investigation and troubleshooting for deviations, equipment issues, and method-related problems.</li><li>Ability to monitor, calibrate, qualify, validate, and perform preventive maintenance on laboratory equipment.</li><li>Working knowledge of quality systems, ISO standards, ISO procedures, and GMP requirements.</li><li>Strong attention to detail and accuracy in testing, documentation, and data analysis.</li><li>Effective written and verbal communication skills and the ability to work collaboratively in a team environment.</li><li>Demonstrated investigative and problem-solving abilities in a regulated or structured laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a regulated laboratory environment, including GLP and cGMP settings, is a plus.</li><li>Experience in microbiology laboratories, including handling media, environmental monitoring, and microbial analysis.</li><li>Familiarity with quality assurance activities such as audits, document control, and quality trending programs.</li><li>Exposure to stability studies, product testing, and continuous improvement initiatives.</li><li>Experience working with raw materials inspection, analysis, and adherence to ISO standards and procedures.</li><li>Ability to manage multiple tasks in a fast-paced laboratory environment while maintaining high quality standards.</li><li>Comfort working on projects related to pharmaceuticals, nutritional products, veterinary instruments, diagnostics, and agricultural chemicals.</li><li>Interest in animal health, including products that support livestock, companion animals, and racehorses.</li></ul>Work EnvironmentThe role is based in a laboratory environment within a global animal safety and health-focused facility. The site manufactures and distributes veterinary instruments, diagnostics, pharmaceuticals, nutritional supplements, disinfectants, and agricultural chemicals that protect the health of livestock, companion animals, and racehorses. The laboratory operates under GLP, cGMP, ISO standards, and established SOPs, with a strong emphasis on safety, cleanliness, and organization. You will work with microbiology laboratories, environmental monitoring systems, aseptic techniques, and a variety of analytical equipment that requires regular calibration, qualification, and validation. The organization has recently restructured and operates under new leadership, offering the opportunity to join a growing team engaged in exciting pharmaceutical and nutritional projects across multiple industries. The culture emphasizes collaboration, continuous improvement, and adherence to quality and safety procedures in a professional, team-oriented setting.Job Type &amp; LocationThis is a Contract to Hire position based out of Lexington, KY.Pay and BenefitsThe pay range for this position is $22.06 - $22.06/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Lexington,KY.Application DeadlineThis position is anticipated to close on Jul 26, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control ManagerJob DescriptionThis role oversees the Quality Control program for federal and military construction projects, ensuring all work complies with contract documents, project specifications, and government quality standards. The Quality Control Manager develops, implements, and maintains project-specific Quality Control Plans while coordinating closely with project teams, subcontractors, and government representatives. This position plays a key role in managing quality documentation, leading inspections, and supporting successful project delivery from start-up through closeout.Responsibilities<ul><li>Oversee the Quality Control program for federal and military construction projects from pre-construction through project closeout.</li><li>Develop, implement, and maintain project-specific Quality Control Plans in accordance with contract requirements and federal standards.</li><li>Manage quality documentation including submittal registers, testing logs, inspection reports, deficiency logs, and rework tracking.</li><li>Conduct and lead Preparatory, Initial, and Follow-Up inspections as part of the Three Phases of Control process.</li><li>Coordinate all testing, inspections, and quality documentation with project teams, subcontractors, and government representatives.</li><li>Ensure all work complies with contract documents, project specifications, and applicable government quality standards.</li><li>Utilize RMS, ECMS, NAVFAC, and/or USACE quality management systems to manage and report quality activities.</li><li>Lead Quality Control meetings and provide regular quality-related reporting to project stakeholders.</li><li>Manage project closeout documentation, including as-built records, warranties, and turnover packages.</li><li>Work collaboratively with Project Managers, Superintendents, owners, and government personnel to resolve quality issues and maintain compliance.</li><li>Support a safety-first culture by integrating quality control processes with site safety practices.</li><li>Contribute to continuous improvement of quality control procedures and best practices across multiple projects.</li></ul>Essential Skills<ul><li>2–5 years of Quality Control experience in construction, preferably on federal or military projects.</li><li>Experience supporting NAVFAC, USACE, DoD, or other federal construction projects.</li><li>Hands-on experience maintaining Quality Control Plans, testing logs, submittal registers, and project closeout documentation.</li><li>Experience with RMS and/or ECMS quality control systems.</li><li>Strong written communication and documentation skills, with the ability to produce clear and accurate reports.</li><li>Proven ability to manage multiple quality control activities simultaneously on active construction sites.</li><li>Demonstrated understanding of Construction Quality Control (CQC) management processes for federal and military projects.</li><li>Ability to lead and document the Three Phases of Control, including Preparatory, Initial, and Follow-Up inspections.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Construction Management, Engineering, Architecture, or a related field preferred.</li><li>Degree may offset some years of experience for candidates with strong certifications and federal construction exposure.</li><li>Experience with NAVFAC and USACE quality control processes and systems strongly preferred.</li><li>Military construction experience highly preferred.</li><li>Background as a Veteran, Seabee, or Army Corps/Combat Engineer considered a plus.</li><li>OSHA 30 certification preferred.</li><li>EM-385 40-Hour training preferred.</li><li>Competent Person certifications preferred.</li><li>Hazwoper training preferred.</li><li>Ability to travel to various project locations and work in a project-to-project environment.</li><li>Strong collaboration skills with project teams, subcontractors, and government representatives.</li></ul>Work EnvironmentProject schedules typically follow either a 4/10 schedule (four 10-hour days) or a 5/8 schedule (five 8-hour days), depending on project requirements. Workdays generally start early, with typical start times between 5:30 AM and 7:00 AM based on site access and operational needs. Most initial projects are located throughout Southern California. Assignments within San Diego County, including sites such as Camp Pendleton and Miramar, are considered local and generally do not include per diem or mileage reimbursement. For projects outside San Diego County, employees may be eligible for per diem in accordance with project requirements and applicable GSA guidelines. Potential project locations include China Lake, 29 Palms, Yuma, El Centro, Los Angeles, Travis AFB, and other military installations. The employer is open to candidates based outside California, particularly experienced federal construction professionals who are accustomed to traveling from project to project. The work environment emphasizes a supportive, safety-first culture, with a continuous pipeline of projects and opportunities for long-term growth within a respected federal construction team.Job Type &amp; LocationThis is a Contract to Hire position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $45.00 - $55.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in San Diego,CA.Application DeadlineThis position is anticipated to close on Aug 6, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Manager

<h1>Quality Control Manager</h1>Federal &amp; Military Construction<h2>About Us</h2>We are a respected federal construction contractor specializing in the delivery of complex design-build and construction projects for military, government, and federal agency clients throughout the United States. Our team is known for its commitment to quality, safety, integrity, and mission-focused project execution. With a strong backlog of work and long-standing relationships across federal agencies, we offer employees the opportunity to work on meaningful projects that support the nation's military infrastructure while building rewarding careers in a collaborative, growth-oriented environment.<hr><h2>Position Summary</h2>We are seeking a Quality Control Manager to oversee and manage Quality Control (QC) programs on federal and military construction projects. This individual will be responsible for developing, implementing, and maintaining project-specific Quality Control Plans while ensuring strict compliance with contract requirements, government regulations, and project specifications.The ideal candidate possesses strong construction quality management experience, exceptional documentation skills, and the ability to effectively collaborate with project teams, subcontractors, and government representatives to deliver projects that meet the highest standards of quality and performance.<hr><h2>Key Responsibilities</h2><ul><li>Develop, implement, and maintain project Quality Control Plans.</li><li>Administer and maintain submittal registers, test logs, inspection reports, deficiency logs, and rework-tracking documentation.</li><li>Conduct and lead Preparatory, Initial, and Follow-Up Inspections in accordance with the Three Phases of Control process.</li><li>Coordinate quality testing, inspections, and documentation with project teams, subcontractors, third-party testing agencies, and government representatives.</li><li>Ensure all work complies with contract documents, project specifications, applicable codes, and government quality standards.</li><li>Manage project quality records, closeout documentation, warranties, as-built drawings, and turnover packages.</li><li>Utilize RMS, ECMS, NAVFAC, USACE, and other government quality management systems as required.</li><li>Lead quality control meetings and prepare quality-related reports for project stakeholders.</li><li>Identify, document, and track deficiencies through resolution.</li><li>Collaborate closely with Project Managers, Superintendents, Owners, and Government personnel to maintain project compliance and quality expectations.</li></ul><hr><h2>Qualifications</h2><h3>Required</h3><ul><li>Strong written communication, organization, and documentation skills.</li><li>Experience maintaining Quality Control Plans, testing logs, submittal registers, inspection records, and closeout documentation.</li><li>Ability to interpret construction drawings, specifications, and contract requirements.</li><li>Proven ability to manage multiple priorities in a fast-paced construction environment.</li></ul><h3>Preferred</h3><ul><li>2-5 years of Quality Control experience in construction.</li><li>Experience supporting NAVFAC, USACE, DoD, or other federal construction projects.</li><li>Bachelor's Degree in Construction Management, Engineering, Architecture, or a related field.</li><li>Experience utilizing RMS and/or ECMS platforms.</li><li>Military construction experience.</li><li>OSHA 30 certification.</li><li>QCM or Construction Quality Control (CQC) Management experience on federal projects.</li></ul><h3>Additional Preferred Certifications &amp; Experience</h3><ul><li>EM 385-1-1 40-Hour Training</li><li>Competent Person Certifications</li><li>HAZWOPER Training</li><li>Veteran, Seabee, Army Corps, or Combat Engineer background</li></ul><hr><h2>Work Environment &amp; Travel</h2>Project schedules typically follow either a 4/10 or 5/8 work schedule, with start times generally between 5:30 AM and 7:00 AM depending on project requirements.Initial assignments are expected to be located throughout Southern California, including San Diego County. Per diem or mileage reimbursement may not apply to local assignments. Employees assigned to projects outside San Diego County may be eligible for per diem in accordance with project requirements and applicable GSA guidelines.Job Type &amp; LocationThis is a Contract to Hire position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $45.00 - $55.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in San Diego,CA.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control &amp; Safety ManagerJob DescriptionThe Quality Control &amp; Safety Manager oversees the quality and safety of industrial hoses and fittings received from vendors, ensuring they meet internal standards and comply with all relevant regulatory requirements. This role manages and works alongside a Quality Technician to perform inspections, leads the culture of quality and safety across the facility, and ensures warehouse operations follow established safety practices. The position offers hands-on involvement on the distribution floor and the opportunity to grow into an engineering or mid-management role with broader quality responsibilities across multiple facilities.Responsibilities<ul><li>Oversee and perform quality inspections of industrial hoses and fittings received from vendors to ensure they meet company standards and regulatory requirements.</li><li>Manage and work side-by-side with the Quality Technician to plan, execute, and document inspection activities.</li><li>Develop, promote, and lead a strong culture of quality and safety for all employees within the distribution facility.</li><li>Monitor and enforce warehouse safety practices, ensuring daily operations align with internal policies and external regulations.</li><li>Prepare and maintain smaller-scale safety and compliance reports, including incident reports and related investigations, while coordinating with the parent company on annual safety and OSHA reporting.</li><li>Ensure compliance with applicable regulatory requirements such as REACH, RoHS, CMRT, PFAS, Prop 65, TSCA, and USMCA by maintaining accurate documentation and records.</li><li>Complete and submit compliance forms and documentation for clients, including state regulatory forms and other required quality and safety documentation.</li><li>Support and participate in safety committees and initiatives, contributing to continuous improvement in environmental health and safety (EHS).</li><li>Implement and support quality assurance and quality control processes, including corrective and preventive action (CAPA) and return material authorization (RMA) procedures.</li><li>Investigate quality and safety issues, identify root causes, and develop corrective action plans to prevent recurrence.</li><li>Provide or support safety training for employees, leveraging resources such as safety videos and guidance from the parent organization.</li><li>Collaborate with leadership and peers to adapt to the existing culture, understand current processes, and then recommend improvements in a thoughtful, humble manner.</li><li>Contribute to long-term quality strategy with potential expansion into managing quality operations for additional facilities in other locations.</li></ul>Essential Skills<ul><li>2–3+ years of experience in quality control or quality assurance at a technician level.</li><li>Hands-on experience with quality control of industrial products, including inspection and documentation.</li><li>Experience with safety practices in a warehouse or distribution environment.</li><li>Background in compliance with state regulations and completion of compliance forms for clients.</li><li>Familiarity with OSHA requirements and safety reporting processes.</li><li>Experience participating in or serving on a safety committee.</li><li>Knowledge of regulatory compliance frameworks such as REACH, RoHS, CMRT, PFAS, Prop 65, TSCA, and USMCA.</li><li>Experience with EHS (environmental health and safety) practices.</li><li>Experience with quality assurance and QC processes, including CAPA (corrective and preventive action) and RMA procedures.</li><li>Ability to conduct incident reporting and investigations and document findings clearly and accurately.</li><li>Strong attention to detail and commitment to maintaining high quality and safety standards.</li><li>Ability to work collaboratively on the distribution floor with technicians and operations staff.</li><li>Demonstrated humility and willingness to understand existing processes and culture before driving change.</li></ul>Additional Skills &amp; Qualifications<ul><li>ASQ certification is preferred and demonstrates a strong foundation in quality principles.</li><li>Experience with ASQ methodologies or related quality certifications.</li><li>Exposure to or interest in career growth toward an engineering or mid-management role.</li><li>Interest in expanding responsibilities to manage quality for multiple facilities in different locations.</li><li>Comfort working in a private equity–owned environment with support from a parent organization on high-level safety programs.</li><li>Strong communication skills to effectively convey quality and safety expectations to employees at all levels.</li></ul>Work EnvironmentThis role is based in a distribution facility with a hands-on, floor-focused work style. The Quality Control &amp; Safety Manager spends a significant amount of time on the warehouse floor working side-by-side with the Quality Technician and operational staff. The environment is small and tight-knit, with many employees having long tenure and a culture that values humility, collaboration, and continuous improvement. The parent organization provides support for high-level safety programs, including annual safety reports and safety video training. The position offers opportunities for professional growth into broader quality responsibilities and potential leadership roles across multiple facilities.#LI-MH3Job Type &amp; LocationThis is a Permanent position based out of Portland, OR.Pay and BenefitsThe pay range for this position is $70000.00 - $80000.00/yr.Quarterly Profit-Sharing bonus
Multiple Medical, Dental, Vision insurance options

Basic Life insurance, Short-term Disability and Long-term Disability 100% paid by employer
401(k) with employer match
Paid Time Off
Paid Holidays
Employee Assistance ProgramWorkplace TypeThis is a fully onsite position in Portland,OR.Application DeadlineThis position is anticipated to close on Jul 28, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control ManagerJob DescriptionThis role oversees the Quality Control program for federal and military construction projects, ensuring all work complies with contract documents, project specifications, and government quality standards. The Quality Control Manager develops, implements, and maintains project-specific Quality Control Plans while coordinating closely with project teams, subcontractors, and government representatives. This position plays a key role in managing quality documentation, leading inspections, and supporting successful project delivery from start-up through closeout.Responsibilities<ul><li>Oversee the Quality Control program for federal and military construction projects from pre-construction through project closeout.</li><li>Develop, implement, and maintain project-specific Quality Control Plans in accordance with contract requirements and federal standards.</li><li>Manage quality documentation including submittal registers, testing logs, inspection reports, deficiency logs, and rework tracking.</li><li>Conduct and lead Preparatory, Initial, and Follow-Up inspections as part of the Three Phases of Control process.</li><li>Coordinate all testing, inspections, and quality documentation with project teams, subcontractors, and government representatives.</li><li>Ensure all work complies with contract documents, project specifications, and applicable government quality standards.</li><li>Utilize RMS, ECMS, NAVFAC, and/or USACE quality management systems to manage and report quality activities.</li><li>Lead Quality Control meetings and provide regular quality-related reporting to project stakeholders.</li><li>Manage project closeout documentation, including as-built records, warranties, and turnover packages.</li><li>Work collaboratively with Project Managers, Superintendents, owners, and government personnel to resolve quality issues and maintain compliance.</li><li>Support a safety-first culture by integrating quality control processes with site safety practices.</li><li>Contribute to continuous improvement of quality control procedures and best practices across multiple projects.</li></ul>Essential Skills<ul><li>2–5 years of Quality Control experience in construction, preferably on federal or military projects.</li><li>Experience supporting NAVFAC, USACE, DoD, or other federal construction projects.</li><li>Hands-on experience maintaining Quality Control Plans, testing logs, submittal registers, and project closeout documentation.</li><li>Experience with RMS and/or ECMS quality control systems.</li><li>Strong written communication and documentation skills, with the ability to produce clear and accurate reports.</li><li>Proven ability to manage multiple quality control activities simultaneously on active construction sites.</li><li>Demonstrated understanding of Construction Quality Control (CQC) management processes for federal and military projects.</li><li>Ability to lead and document the Three Phases of Control, including Preparatory, Initial, and Follow-Up inspections.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Construction Management, Engineering, Architecture, or a related field preferred.</li><li>Degree may offset some years of experience for candidates with strong certifications and federal construction exposure.</li><li>Experience with NAVFAC and USACE quality control processes and systems strongly preferred.</li><li>Military construction experience highly preferred.</li><li>Background as a Veteran, Seabee, or Army Corps/Combat Engineer considered a plus.</li><li>OSHA 30 certification preferred.</li><li>EM-385 40-Hour training preferred.</li><li>Competent Person certifications preferred.</li><li>Hazwoper training preferred.</li><li>Ability to travel to various project locations and work in a project-to-project environment.</li><li>Strong collaboration skills with project teams, subcontractors, and government representatives.</li></ul>Work EnvironmentProject schedules typically follow either a 4/10 schedule (four 10-hour days) or a 5/8 schedule (five 8-hour days), depending on project requirements. Workdays generally start early, with typical start times between 5:30 AM and 7:00 AM based on site access and operational needs. Most initial projects are located throughout Southern California. Assignments within San Diego County, including sites such as Camp Pendleton and Miramar, are considered local and generally do not include per diem or mileage reimbursement. For projects outside San Diego County, employees may be eligible for per diem in accordance with project requirements and applicable GSA guidelines. Potential project locations include China Lake, 29 Palms, Yuma, El Centro, Los Angeles, Travis AFB, and other military installations. The employer is open to candidates based outside California, particularly experienced federal construction professionals who are accustomed to traveling from project to project. The work environment emphasizes a supportive, safety-first culture, with a continuous pipeline of projects and opportunities for long-term growth within a respected federal construction team.Job Type &amp; LocationThis is a Contract to Hire position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $45.00 - $55.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in San Diego,CA.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control ManagerJob DescriptionThis role oversees the Quality Control program for federal and military construction projects, ensuring all work complies with contract documents, project specifications, and government quality standards. The Quality Control Manager develops, implements, and maintains project-specific Quality Control Plans while coordinating closely with project teams, subcontractors, and government representatives. This position plays a key role in managing quality documentation, leading inspections, and supporting successful project delivery from start-up through closeout.Responsibilities<ul><li>Oversee the Quality Control program for federal and military construction projects from pre-construction through project closeout.</li><li>Develop, implement, and maintain project-specific Quality Control Plans in accordance with contract requirements and federal standards.</li><li>Manage quality documentation including submittal registers, testing logs, inspection reports, deficiency logs, and rework tracking.</li><li>Conduct and lead Preparatory, Initial, and Follow-Up inspections as part of the Three Phases of Control process.</li><li>Coordinate all testing, inspections, and quality documentation with project teams, subcontractors, and government representatives.</li><li>Ensure all work complies with contract documents, project specifications, and applicable government quality standards.</li><li>Utilize RMS, ECMS, NAVFAC, and/or USACE quality management systems to manage and report quality activities.</li><li>Lead Quality Control meetings and provide regular quality-related reporting to project stakeholders.</li><li>Manage project closeout documentation, including as-built records, warranties, and turnover packages.</li><li>Work collaboratively with Project Managers, Superintendents, owners, and government personnel to resolve quality issues and maintain compliance.</li><li>Support a safety-first culture by integrating quality control processes with site safety practices.</li><li>Contribute to continuous improvement of quality control procedures and best practices across multiple projects.</li></ul>Essential Skills<ul><li>2–5 years of Quality Control experience in construction, preferably on federal or military projects.</li><li>Experience supporting NAVFAC, USACE, DoD, or other federal construction projects.</li><li>Hands-on experience maintaining Quality Control Plans, testing logs, submittal registers, and project closeout documentation.</li><li>Experience with RMS and/or ECMS quality control systems.</li><li>Strong written communication and documentation skills, with the ability to produce clear and accurate reports.</li><li>Proven ability to manage multiple quality control activities simultaneously on active construction sites.</li><li>Demonstrated understanding of Construction Quality Control (CQC) management processes for federal and military projects.</li><li>Ability to lead and document the Three Phases of Control, including Preparatory, Initial, and Follow-Up inspections.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Construction Management, Engineering, Architecture, or a related field preferred.</li><li>Degree may offset some years of experience for candidates with strong certifications and federal construction exposure.</li><li>Experience with NAVFAC and USACE quality control processes and systems strongly preferred.</li><li>Military construction experience highly preferred.</li><li>Veteran, Seabee, or Army Corps/Combat Engineer considered a plus.</li><li>OSHA 30 certification preferred.</li><li>EM-385 40-Hour training preferred.</li><li>Competent Person certifications preferred.</li><li>Hazwoper training preferred.</li><li>Ability to travel to various project locations and work in a project-to-project environment.</li><li>Strong collaboration skills with project teams, subcontractors, and government representatives.</li></ul>Work EnvironmentProject schedules typically follow either a 4/10 schedule (four 10-hour days) or a 5/8 schedule (five 8-hour days), depending on project requirements. Workdays generally start early, with typical start times between 5:30 AM and 7:00 AM based on site access and operational needs. Most initial projects are located throughout Southern California. Assignments within San Diego County, including sites such as Camp Pendleton and Miramar, are considered local and generally do not include per diem or mileage reimbursement. For projects outside San Diego County, employees may be eligible for per diem in accordance with project requirements and applicable GSA guidelines. Potential project locations include China Lake, 29 Palms, Yuma, El Centro, Los Angeles, Travis AFB, and other military installations. The employer is open to candidates based outside California, particularly experienced federal construction professionals who are accustomed to traveling from project to project. The work environment emphasizes a supportive, safety-first culture, with a continuous pipeline of projects and opportunities for long-term growth within a respected federal construction team.Job Type &amp; LocationThis is a Contract to Hire position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $45.00 - $55.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in San Diego,CA.Application DeadlineThis position is anticipated to close on Aug 6, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control ManagerJob DescriptionThis role leads the quality control program for federal and military construction projects, ensuring all work meets contract requirements, project specifications, and government quality standards. The Quality Control Manager develops, implements, and maintains project-specific Quality Control Plans, oversees inspections and testing, and manages all quality documentation throughout the project lifecycle. This position works closely with project teams, subcontractors, and government representatives to drive a safety-first, compliance-focused culture while supporting successful project delivery and closeout.Responsibilities<ul><li>Oversee and manage the Quality Control program for federal and military construction projects from project start through closeout.</li><li>Develop, implement, and maintain project-specific Quality Control Plans in alignment with contract documents and government requirements.</li><li>Manage and maintain submittal registers, testing logs, inspection reports, deficiency logs, and rework tracking to ensure accurate and timely documentation.</li><li>Conduct and lead Preparatory, Initial, and Follow-Up inspections as part of the Three Phases of Control process.</li><li>Coordinate all testing, inspections, and quality-related documentation with project teams, subcontractors, and government representatives.</li><li>Ensure all work complies with contract documents, project specifications, and applicable government quality standards and procedures.</li><li>Utilize RMS, ECMS, NAVFAC, and/or USACE quality management systems to document and track quality control activities.</li><li>Lead regular quality control meetings and provide clear, timely quality-related reporting to project stakeholders.</li><li>Manage project closeout documentation, including as-built records, warranties, and turnover packages, to ensure complete and accurate project delivery.</li><li>Work collaboratively with Project Managers, Superintendents, owners, and government personnel to resolve quality issues and maintain high standards.</li><li>Support a safety-first culture by integrating quality control processes with site safety practices and expectations.</li><li>Participate in planning and coordination meetings to identify quality requirements and potential risks early in the project.</li><li>Monitor ongoing work to identify deficiencies, track corrective actions, and verify completion of rework in accordance with quality standards.</li></ul>Essential Skills<ul><li>2–5 years of Quality Control experience preferred, ideally on federal or military construction projects.</li><li>Demonstrated experience in Construction Quality Control (CQC) Management on federal and/or military construction projects.</li><li>Experience supporting NAVFAC, USACE, DoD, or other federal construction projects highly preferred.</li><li>Proven ability to develop, implement, and maintain Quality Control Plans for construction projects.</li><li>Strong experience managing quality documentation, including QC Plans, submittal registers, testing logs, deficiency logs, and project closeout documentation.</li><li>Experience with RMS and/or ECMS quality management systems strongly preferred.</li><li>Familiarity with NAVFAC and USACE quality control processes and requirements.</li><li>Military construction experience highly preferred.</li><li>Strong written communication and documentation skills required, with the ability to produce clear, accurate reports and records.</li><li>Ability to lead and conduct Preparatory, Initial, and Follow-Up inspections within the Three Phases of Control process.</li><li>Ability to coordinate effectively with project teams, subcontractors, and government representatives in a fast-paced construction environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Construction Management, Engineering, Architecture, or a related field preferred.</li><li>A relevant degree may offset some years of experience for candidates with strong certifications and federal construction exposure.</li><li>Experience with NAVFAC, USACE, or other federal agency quality management systems is a plus.</li><li>Veteran, Seabee, or Army Corps/Combat Engineer is considered a plus.</li><li>OSHA 30 certification preferred but not required.</li><li>EM-385 40-Hour training preferred but not required.</li><li>Competent Person certifications preferred but not required.</li><li>Hazwoper training preferred but not required.</li><li>Ability to travel to various project sites as needed, including extended stays on out-of-area projects.</li><li>Comfort working in a structured, compliance-driven environment with detailed quality and documentation standards.</li></ul>Work EnvironmentProject schedules typically follow either a 4/10 schedule (four 10-hour days) or a 5/8 schedule (five 8-hour days), depending on project requirements. Workdays generally start early, with typical start times between 5:30 a.m. and 7:00 a.m., driven by site access and operational needs. Most initial projects are located throughout Southern California, with local assignments commonly within San Diego County, including installations such as Camp Pendleton and Miramar. These local assignments generally do not receive per diem or mileage reimbursement. For projects outside San Diego County, employees may be eligible for per diem in accordance with project requirements and applicable GSA guidelines. Potential project locations may include China Lake, 29 Palms, Yuma, El Centro, Los Angeles, Travis Air Force Base, and other military installations. The organization is open to candidates based outside California, particularly those with federal construction experience who are accustomed to traveling from project to project. The work environment is field-focused and construction-site based, emphasizing a supportive, safety-first culture with a continuous pipeline of federal projects and long-term growth opportunities for high-performing team members.Job Type &amp; LocationThis is a Contract to Hire position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $45.00 - $55.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in San Diego,CA.Application DeadlineThis position is anticipated to close on Aug 7, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control ManagerJob DescriptionThis role leads the full quality control program for a major $127 million renovation project in Fairfax, VA, spanning demolition, restructuring, and new vertical construction over an expected duration of more than three years. The Quality Control Manager ensures that all construction activities meet contractual, regulatory, and safety requirements while coordinating closely with project leadership, field teams, and stakeholders to deliver a high-quality, compliant, and well-documented project.Responsibilities<ul><li>Implement and manage the entire project quality control (QC) program for a large-scale renovation and vertical construction project.</li><li>Oversee quality control activities during demolition, restructuring, and new construction phases to ensure compliance with project specifications and applicable standards.</li><li>Attend all post-award conferences, Contractor Quality Control (CQC) plan meetings, coordination meetings, and mutual understanding meetings to represent and lead QC efforts.</li><li>Plan, schedule, and conduct regular CQC meetings with project teams and subcontractors to review quality requirements, address issues, and drive continuous improvement.</li><li>Perform and document the three phases of the quality control process (preparatory, initial, and follow-up inspections) for all definable features of work.</li><li>Review, evaluate, and approve submittals to ensure they comply with contract documents, specifications, and applicable codes before work proceeds.</li><li>Ensure all required testing is properly scheduled, performed, documented, and tracked, including coordinating with testing agencies and laboratories as needed.</li><li>Monitor field work to verify adherence to approved submittals, drawings, specifications, and quality standards, and initiate corrective actions when necessary.</li><li>Interpret and review blueprints, drawings, and technical documents to identify quality requirements and potential issues before and during construction.</li><li>Prepare, maintain, and organize QC documentation, including inspection reports, test results, non-conformance reports, and corrective action records.</li><li>Coordinate with project management, superintendents, and inspectors to resolve quality-related issues and maintain alignment with project objectives.</li><li>Support compliance with OSHA and other safety requirements by integrating safety considerations into QC processes and field inspections.</li><li>Collaborate on local, state, and federal project requirements to ensure that all regulatory and contractual quality standards are met.</li><li>Provide guidance and oversight to inspectors and field personnel on quality expectations, procedures, and best practices.</li><li>Contribute to a culture of ownership and accountability by promoting high standards of workmanship and proactive problem solving across the project team.</li></ul>Essential Skills<ul><li>Proven experience in vertical construction quality control, including work on demolition, restructuring, and new construction projects.</li><li>Demonstrated ability to implement and manage a comprehensive QC program on large construction projects.</li><li>Hands-on experience with Contractor Quality Control (CQC) processes, including planning and conducting CQC meetings.</li><li>Ability to perform the three phases of quality control (preparatory, initial, and follow-up) and document each phase thoroughly.</li><li>Strong skills in reviewing and approving submittals for compliance with contract documents and specifications.</li><li>Experience ensuring that all required testing is scheduled, performed, and documented in accordance with project requirements.</li><li>Knowledge of OSHA compliance requirements and the ability to support safe work practices through QC activities.</li><li>Familiarity with USACE (U.S. Army Corps of Engineers) quality control standards and procedures.</li><li>Experience working as an inspector or quality control manager on local, state, or federal construction projects.</li><li>Ability to read and interpret blueprints, drawings, and technical documents and to identify and communicate quality-related issues.</li><li>Certified Quality Control Manager (QCM) or equivalent QC certification.</li><li>Strong organizational and documentation skills to manage QC records, reports, and testing documentation.</li><li>Effective communication skills to collaborate with project managers, superintendents, inspectors, and field personnel.</li><li>Ability to maintain consistency and longevity in vertical construction roles, demonstrating stable and reliable project involvement.</li></ul>Additional Skills &amp; Qualifications<ul><li>Professional Engineer (PE) license with a relevant degree is highly valued and may be considered in lieu of certain inspector experience.</li><li>Experience as an inspector with a track record of long-term involvement in vertical construction projects.</li><li>Experience in construction quality control on local, state, or federal projects, particularly those involving complex renovations and new vertical construction.</li><li>Exposure to or familiarity with ESOP (Employee Stock Ownership Plan) environments or ownership-minded cultures.</li><li>Strong problem-solving abilities and a proactive approach to identifying and resolving quality issues before they impact schedule or cost.</li><li>Ability to mentor and support field teams in understanding and meeting quality expectations.</li></ul>Work EnvironmentThis role is based on a construction site in Fairfax, VA, working on a large, multi-year renovation and vertical construction project. The Quality Control Manager works on-site five days a week during the day shift, closely interacting with project managers, project executives, superintendents, inspectors, and field crews. The environment involves active demolition, restructuring, and new construction activities, requiring regular field presence, coordination with testing agencies, and hands-on oversight of work in progress. The project team uses innovative and cutting-edge technology to plan, monitor, and document construction activities. The culture emphasizes learning from experienced project leaders who lead by example, a strong sense of ownership among team members, and the opportunity to participate in an employee ownership structure, fostering a collaborative and accountable work atmosphere.Job Type &amp; LocationThis is a Contract to Hire position based out of Annandale, VA.Pay and BenefitsThe pay range for this position is $85000.00 - $130000.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Annandale,VA.Application DeadlineThis position is anticipated to close on Aug 4, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h1>Quality Control Manager</h1>Federal &amp; Military Construction<h2>About Us</h2>We are a respected federal construction contractor specializing in the delivery of complex design-build and construction projects for military, government, and federal agency clients throughout the United States. Our team is known for its commitment to quality, safety, integrity, and mission-focused project execution. With a strong backlog of work and long-standing relationships across federal agencies, we offer employees the opportunity to work on meaningful projects that support the nation's military infrastructure while building rewarding careers in a collaborative, growth-oriented environment.<hr><h2>Position Summary</h2>We are seeking a Quality Control Manager to oversee and manage Quality Control (QC) programs on federal and military construction projects. This individual will be responsible for developing, implementing, and maintaining project-specific Quality Control Plans while ensuring strict compliance with contract requirements, government regulations, and project specifications.The ideal candidate possesses strong construction quality management experience, exceptional documentation skills, and the ability to effectively collaborate with project teams, subcontractors, and government representatives to deliver projects that meet the highest standards of quality and performance.<hr><h2>Key Responsibilities</h2><ul><li>Develop, implement, and maintain project Quality Control Plans.</li><li>Administer and maintain submittal registers, test logs, inspection reports, deficiency logs, and rework-tracking documentation.</li><li>Conduct and lead Preparatory, Initial, and Follow-Up Inspections in accordance with the Three Phases of Control process.</li><li>Coordinate quality testing, inspections, and documentation with project teams, subcontractors, third-party testing agencies, and government representatives.</li><li>Ensure all work complies with contract documents, project specifications, applicable codes, and government quality standards.</li><li>Manage project quality records, closeout documentation, warranties, as-built drawings, and turnover packages.</li><li>Utilize RMS, ECMS, NAVFAC, USACE, and other government quality management systems as required.</li><li>Lead quality control meetings and prepare quality-related reports for project stakeholders.</li><li>Identify, document, and track deficiencies through resolution.</li><li>Collaborate closely with Project Managers, Superintendents, Owners, and Government personnel to maintain project compliance and quality expectations.</li></ul><hr><h2>Qualifications</h2><h3>Required</h3><ul><li>Strong written communication, organization, and documentation skills.</li><li>Experience maintaining Quality Control Plans, testing logs, submittal registers, inspection records, and closeout documentation.</li><li>Ability to interpret construction drawings, specifications, and contract requirements.</li><li>Proven ability to manage multiple priorities in a fast-paced construction environment.</li></ul><h3>Preferred</h3><ul><li>2-5 years of Quality Control experience in construction.</li><li>Experience supporting NAVFAC, USACE, DoD, or other federal construction projects.</li><li>Bachelor's Degree in Construction Management, Engineering, Architecture, or a related field.</li><li>Experience utilizing RMS and/or ECMS platforms.</li><li>Military construction experience.</li><li>OSHA 30 certification.</li><li>QCM or Construction Quality Control (CQC) Management experience on federal projects.</li></ul><h3>Additional Preferred Certifications &amp; Experience</h3><ul><li>EM 385-1-1 40-Hour Training</li><li>Competent Person Certifications</li><li>HAZWOPER Training</li><li>Veteran, Seabee, Army Corps, or Combat Engineer background</li></ul><hr><h2>Work Environment &amp; Travel</h2>Project schedules typically follow either a 4/10 or 5/8 work schedule, with start times generally between 5:30 AM and 7:00 AM depending on project requirements.Initial assignments are expected to be located throughout Southern California, including San Diego County. Per diem or mileage reimbursement may not apply to local assignments. Employees assigned to projects outside San Diego County may be eligible for per diem in accordance with project requirements and applicable GSA guidelines.Job Type &amp; LocationThis is a Contract to Hire position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $45.00 - $55.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in San Diego,CA.Application DeadlineThis position is anticipated to close on Jul 28, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control Manager – Great Lakes (Site Safety, Quality &amp; Construction Manager)Job DescriptionThe Site Safety, Quality &amp; Construction Manager is a full‑time, on‑site role overseeing construction operations, safety compliance, and quality control on a federal healthcare roofing project in North Chicago, IL. This position serves simultaneously as the Site Safety and Health Officer (SSHO), Competent Person, and Superintendent/Construction Quality Control (CQC) Manager, ensuring strict adherence to OSHA 29 CFR 1926, USACE EM 385‑1‑1, and applicable VA and NAVFAC requirements. The role focuses on managing daily field activities, supervising subcontractors, administering the Accident Prevention Plan (APP), conducting inspections, and delivering safe, compliant, and high‑quality work in an occupied medical facility.Responsibilities<ul><li>Oversee day‑to‑day construction operations for the roofing project at a federal healthcare facility, ensuring work is completed safely, efficiently, and to specified quality standards.</li><li>Serve as the Site Safety and Health Officer (SSHO), Competent Person, and Superintendent/CQC Manager with authority over site safety, quality control, and construction activities.</li><li>Ensure full compliance with OSHA 29 CFR 1926, USACE EM 385‑1‑1, and applicable VA and NAVFAC safety and quality requirements throughout all phases of the project.</li><li>Administer and enforce the Accident Prevention Plan (APP), including site‑specific safety procedures, hazard identification, and corrective actions.</li><li>Plan, coordinate, and supervise daily field activities, including scheduling work, sequencing tasks, and aligning resources to meet project milestones.</li><li>Direct and oversee subcontractors, ensuring they follow safety protocols, quality standards, and contract requirements.</li><li>Implement and manage the three‑phase quality control process (Preparatory, Initial, Follow‑Up) for all definable features of work.</li><li>Conduct preparatory meetings to review plans, specifications, safety requirements, and quality standards before work begins.</li><li>Perform initial inspections at the start of each definable feature of work to verify compliance with approved plans, specifications, and safety requirements.</li><li>Carry out follow‑up inspections to confirm that work continues to meet quality standards and that any deficiencies are corrected promptly.</li><li>Manage all inspections, testing, and documentation required under the CQC system, including maintaining accurate records and reports.</li><li>Oversee project closeout quality requirements, ensuring all punch‑list items, testing, and documentation are completed and submitted in accordance with contract standards.</li><li>Coordinate and communicate with project stakeholders to address safety, quality, and construction issues in a timely and professional manner.</li><li>Ensure construction activities are planned and executed in a manner that minimizes disruption to ongoing operations within the occupied medical facility.</li><li>Promote a strong safety culture on site through ongoing safety training, toolbox talks, and reinforcement of best practices.</li><li>Monitor compliance with safety training requirements and verify that all personnel maintain appropriate safety credentials (such as OSHA 30).</li><li>Identify, document, and resolve non‑conformances related to safety and quality, implementing corrective and preventive actions.</li><li>Support the use of NAVFAC eCMS or similar systems for quality documentation and reporting, where applicable.</li></ul>Essential Skills<ul><li>Proven experience in construction safety and quality control on federal construction projects, preferably in healthcare or similarly complex environments.</li><li>Strong background in construction site management, including coordination of daily field activities and supervision of subcontractors.</li><li>Demonstrated expertise in safety compliance with OSHA 29 CFR 1926 and USACE EM 385‑1‑1 standards.</li><li>Experience serving as Site Safety and Health Officer (SSHO) or equivalent safety leadership role on construction projects.</li><li>Hands‑on experience implementing and managing a Construction Quality Control (CQC) system, including the three‑phase control process (Preparatory, Initial, Follow‑Up).</li><li>Ability to administer and enforce an Accident Prevention Plan (APP) and site‑specific safety procedures.</li><li>Strong understanding of federal construction safety and compliance requirements, including VA and NAVFAC standards.</li><li>Proficiency in conducting safety training, toolbox talks, and ongoing safety communication for field personnel.</li><li>Ability to manage inspections, testing, and documentation in a structured and organized manner.</li><li>Effective communication and leadership skills to direct subcontractors and coordinate with project stakeholders.</li><li>Capability to operate as the Competent Person on site, identifying hazards and implementing corrective measures.</li><li>Experience with construction quality control in commercial and healthcare environments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with NAVFAC eCMS or similar electronic construction management and quality documentation systems is preferred.</li><li>OSHA 30‑hour construction safety training or equivalent advanced safety credential is strongly desired.</li><li>background in federal construction projects involving NAVFAC and Department of Veterans Affairs facilities is an advantage.</li><li>Knowledge of health and safety best practices specific to work in occupied medical facilities.</li><li>Familiarity with roofing construction and replacement projects in commercial or institutional settings.</li><li>Strong organizational skills and attention to detail for managing documentation, reporting, and closeout requirements.</li><li>Ability to foster a culture of safety, quality, and compliance across diverse teams and subcontractors.</li></ul>Work EnvironmentThis role is based full‑time on site at a federal healthcare facility in North Chicago, IL, supporting a project to replace the roof on the main hospital building. The work takes place in and around an occupied medical center, requiring careful coordination to minimize disruption to patient care and clinical operations. The environment involves active construction areas, rooftop work, and interaction with hospital staff and other stakeholders, with strict adherence to safety protocols and infection control considerations. The position operates within a federal construction framework, following NAVFAC and Department of Veterans Affairs standards and utilizing technologies such as NAVFAC eCMS for documentation where applicable. Work hours follow typical construction schedules, with the need to be present during core site activities and inspections. Appropriate construction site attire and personal protective equipment are required at all times, reflecting the safety‑focused culture and regulatory demands of the facility.Job Type &amp; LocationThis is a Contract position based out of North Chicago, IL.Pay and BenefitsThe pay range for this position is $40.87 - $48.07/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in North Chicago,IL.Application DeadlineThis position is anticipated to close on Jul 27, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Manager - Great Lakes

Job Title: Quality Control Specialist – Sample Management and Technical WriterJob DescriptionThis Quality Control Specialist role focuses on sample management and technical writing within a large molecule manufacturing plant. The specialist works hands-on in the Quality Control unit, coordinating QC samples for routine and qualification testing, supporting qualification studies through detailed report writing, and providing backup testing as needed. The role collaborates closely with QC Microbiology, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Biologics Process Development teams to ensure timely analysis, inspection readiness, and robust data integrity across all QC activities.Responsibilities<ul><li>Work in Quality Control operations, performing hands-on activities including handling QC samples for routine and qualification testing, technical documentation, and backup testing of QC samples.</li><li>Coordinate QC sample management, including receipt, verification, labeling, storage, and distribution of samples to relevant testing laboratories and functions.</li><li>Compile, organize, and trend test results to support qualification reports and other technical documentation required for large molecule manufacturing.</li><li>Review test records and associated documentation to ensure they are accurate, complete, and compliant with internal procedures and regulatory expectations.</li><li>Support and perform testing of QC samples as needed to meet project timelines and manufacturing schedules.</li><li>Collaborate with the Biologics Process Development team to plan and execute testing activities that support drug substance development and manufacturing.</li><li>Ensure that laboratory incidents, out-of-specification (OOS) results, out-of-trend (OOT) results, deviations, and client complaints related to QC testing are thoroughly investigated and documented.</li><li>Identify root causes for QC-related issues and implement effective corrective and preventive actions (CAPA) within agreed timelines.</li><li>Maintain and periodically review all QC documentation, including SOPs, IOPs, EOPs, STPs, and other controlled documents, in alignment with the documentation control system.</li><li>Ensure timely completion of QC activities according to project plans, and update work plans to accommodate changes in project scope, priorities, or timelines.</li><li>Adhere to ALCOA principles of data integrity and promote compliance with these standards among team members.</li><li>Participate in functional working teams to perform self-assessments of compliance with SOPs, Good Manufacturing Practice (GMP), and data integrity standards.</li><li>Support preparation, execution, and timely closure of audit action plans, escalating concerns and risks as appropriate.</li><li>Support investigations and closure of client and regulatory audit observations related to Quality Control activities.</li><li>Ensure laboratory safety protocols are followed at all times, including aseptic techniques, cleanroom practices, and gowning procedures, and resolve technical issues in the QC lab effectively.</li><li>Support preparation and maintenance of QC documentation used in regulatory filings, including prior approval submissions, renewals, updates, and supplements.</li><li>Monitor QC analytical trends, complaints, failures, deviations, and changes to identify opportunities for process, system, and product improvements.</li><li>Plan and manage QC analytical lab resources to support smooth day-to-day operations and meet business needs.</li><li>Contribute to a culture of quality, compliance, safety, and continuous improvement within the QC organization.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline.</li><li>5–8 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically supporting large molecule products.</li><li>Hands-on experience in Quality Control operations, including sample management, routine and qualification testing, and technical documentation.</li><li>Strong understanding of USDA and USFDA regulations, as well as ICH, EU, and Health Canada regulatory frameworks relevant to biologics manufacturing.</li><li>Knowledge of USP and other pharmacopeial standards applicable to biologics and large molecule products.</li><li>Working knowledge of biologic analytical techniques and validation of analytical methods.</li><li>Experience with GMP environments, including adherence to Good Manufacturing Practice and data integrity standards such as ALCOA.</li><li>Proficiency in deviation management, OOS/OOT investigations, CAPA development, and change control processes.</li><li>Experience in technical writing for qualification reports, SOPs, and other regulated documents.</li><li>Demonstrated ability to support regulatory inspections and third-party audits from a QC perspective.</li><li>Experience working within established quality systems, including qualifications, validations, and product lifecycle quality management.</li><li>Proven ability to lead or coordinate cross-functional teams and build strong working relationships across departments.</li><li>Track record of driving continuous improvement initiatives to enhance efficiency, reduce deviations, and improve product quality.</li><li>Strong organizational skills with the ability to manage multiple projects and timelines in a fast-paced environment.</li><li>Excellent attention to detail, documentation accuracy, and commitment to data integrity.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in bioanalytical and bioassay methods for monoclonal antibodies and other biologic molecules.</li><li>Experience in biopharmaceutical, pharmaceutical, or biotechnology manufacturing, particularly in large molecule and bioprocess environments.</li><li>Familiarity with aseptic techniques, cleanroom operations, and gowning procedures in a regulated manufacturing or laboratory setting.</li><li>Experience with document control systems and structured management of SOPs, IOPs, EOPs, STPs, and other controlled documents.</li><li>Exposure to production and bioprocess operations and an understanding of how QC supports end-to-end manufacturing.</li><li>Experience supporting or authoring documentation for regulatory submissions, including prior approval supplements, renewals, and updates.</li><li>Ability to analyze QC trends and metrics to identify systemic issues and propose process or system enhancements.</li><li>Strong problem-solving skills with the ability to resolve technical issues in the laboratory and support troubleshooting of analytical methods.</li><li>Experience working in or with global organizations and comfort operating within complex, matrixed environments.</li><li>Interest in contributing to an innovation-focused culture that emphasizes scientific excellence, client service, and operational efficiency.</li></ul>Work EnvironmentThe role is based in a large molecule manufacturing environment that includes both the manufacturing floor and Quality Control laboratories. You work closely with biologics process development and production teams in a GMP-regulated setting, supporting biopharmaceutical and biotechnology operations. The QC lab operates under strict safety protocols, including aseptic techniques, cleanroom practices, and gowning procedures, with a strong emphasis on data integrity and compliance. The organization maintains a culture driven by passionate scientists focused on solving complex scientific problems, improving R&amp;D productivity, accelerating time to market, and reducing innovation costs. Safety is central to operations, with shared responsibility and accountability for following safety guidelines, procedures, and SOPs. The environment offers exposure to advanced biologic analytical techniques, qualification and validation activities, and regulatory inspections, providing opportunities for professional growth in a dynamic and innovation-oriented setting.Job Type &amp; LocationThis is a Contract position based out of Baltimore, MD.Pay and BenefitsThe pay range for this position is $36.00 - $36.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Baltimore,MD.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Specialist

<h2>Actively Screening for a Quality Control Specialist to join Medical Laboratory in Norcross, GA!</h2>Job DescriptionThe Quality Control Specialist reviews documentation and quality records to ensure that products and processes meet defined specifications and regulatory requirements. This role focuses on documentation review, quality systems compliance, and product assessments in an industrial or warehouse setting, as well as in a laboratory environment. The specialist supports quality management initiatives, participates in quality and compliance projects, and contributes to continuous improvement efforts across testing and quality assurance processes.Responsibilities<ul><li>Review documentation, including records, procedures, and forms, to ensure quality endpoints and compliance requirements are consistently achieved.</li><li>Actively lead and contribute data relevant to Quality Systems Compliance during periodic Management Review meetings.</li><li>Assist Quality Management in coordinating and actively participating in quality or compliance-related projects.</li><li>Conduct product tests and assessments in an industrial or warehouse setting to verify that specifications are met and that products, materials, or supplies function as intended.</li><li>Perform in-process and final product or result inspections and clearances on the production floor to ensure consistency and adherence to standards.</li><li>Identify product defects or potential issues and determine appropriate actions to resolve these issues.</li><li>Analyze the results of laboratory or usability tests to identify defects and ensure they do not persist in future production or testing cycles.</li><li>Maintain detailed records of product defects and manufacturing issues to help identify and eliminate recurring problems and to provide a clear paper trail for accountability and error reporting.</li><li>Notify supervisors or plant leadership of issues or defect reports to support informed decisions about manufacturing processes and practices.</li><li>Support process improvements throughout testing and quality assurance processes to enhance product quality and reliability.</li><li>Suggest improvements to address potential systemic problems discovered during quality control activities, ensuring products are produced consistently and defects or errors do not persist.</li><li>Participate in structured training by reviewing each testing bench in the laboratory environment to gain a general understanding of workflows.</li><li>Use a training booklet to document learnings, add notes, and capture key information communicated during training.</li><li>Shadow Technologists to understand the testing processes and context for the documentation being reviewed, ensuring accurate and informed quality control review.</li><li>Learn and use relevant computer applications to perform documentation review and quality control tasks effectively.</li><li>Complete competency assessments after the training period to demonstrate understanding of quality control review responsibilities.</li></ul>Essential Skills<ul><li>Experience reviewing documentation, including records, procedures, and forms, for quality and compliance.</li><li>Familiarity with laboratory environments and processes related to quality control and quality assurance.</li><li>At least 1 year of experience within quality control, quality assurance, laboratory operations, document control, chemistry, biology, or related fields.</li><li>Ability to conduct product tests and assessments in industrial or warehouse settings to verify specifications and functionality.</li><li>Strong skills in identifying product defects or potential issues and determining appropriate corrective actions.</li><li>Experience analyzing results from lab or usability tests to identify defects and prevent recurrence.</li><li>Proficiency in maintaining detailed records of product defects and manufacturing issues for traceability and accountability.</li><li>Knowledge of standard operating procedures (SOPs) and Good Manufacturing Practices (GMP).</li><li>Strong data entry skills and attention to detail in documentation and recordkeeping.</li><li>Ability to support and participate in Quality Systems Compliance activities and Management Review meetings.</li><li>Effective communication skills to report issues and collaborate with supervisors and cross-functional teams.</li><li>Associate's degree in a scientific discipline or related field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s or Associate’s degree within a scientific discipline such as chemistry, biology, or a related field.</li><li>Preferred one or more years of Quality Assurance or Quality Control experience in a regulated environment.</li><li>Experience working in a clean and regulated environment.</li><li>Familiarity with quality or compliance-related projects and continuous improvement initiatives.</li><li>Comfort working with multiple departments and areas within a large laboratory setting.</li><li>Ability to learn and use computer applications specific to quality control and documentation review.</li><li>Willingness to participate in structured training programs, including bench-by-bench exposure and competency assessments.</li><li>Strong organizational skills and the ability to manage multiple tasks and documentation streams.</li></ul>Work EnvironmentThis role operates primarily in a laboratory environment focused on quality control review, with no direct testing performed by the specialist. The position also supports product assessments in industrial or warehouse settings and on the production floor. The environment is clean, regulated, and technology-driven, with a large laboratory that includes many departments and opportunities for cross-functional exposure and growth. Training takes place Monday through Friday from 11:00 a.m. to 7:30 p.m., and the regular work schedule runs Wednesday through Saturday from 10:00 p.m. to 8:30 a.m. New employees receive structured training, including exposure to one testing bench at a time, use of a training booklet for notes and reference, shadowing of Technologists to understand testing workflows, and learning relevant computer applications. A competency assessment occurs after approximately three weeks. The company culture is friendly and supportive, offering a clean, regulated setting with a long-term career path, opportunities for permanent conversion, and room for professional development within a large laboratory environment.Job Type &amp; LocationThis is a Contract position based out of NORCROSS, GA.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in NORCROSS,GA.Application DeadlineThis position is anticipated to close on Aug 4, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2>Actively Screening for a Quality Control Specialist to join Medical Laboratory in Norcross, GA!</h2>Job DescriptionThe Quality Control Specialist reviews documentation and quality records to ensure that products and processes meet defined specifications and regulatory requirements. This role focuses on documentation review, quality systems compliance, and product assessments in an industrial or warehouse setting, as well as in a laboratory environment. The specialist supports quality management initiatives, participates in quality and compliance projects, and contributes to continuous improvement efforts across testing and quality assurance processes.Responsibilities<ul><li>Review documentation, including records, procedures, and forms, to ensure quality endpoints and compliance requirements are consistently achieved.</li><li>Actively lead and contribute data relevant to Quality Systems Compliance during periodic Management Review meetings.</li><li>Assist Quality Management in coordinating and actively participating in quality or compliance-related projects.</li><li>Conduct product tests and assessments in an industrial or warehouse setting to verify that specifications are met and that products, materials, or supplies function as intended.</li><li>Perform in-process and final product or result inspections and clearances on the production floor to ensure consistency and adherence to standards.</li><li>Identify product defects or potential issues and determine appropriate actions to resolve these issues.</li><li>Analyze the results of laboratory or usability tests to identify defects and ensure they do not persist in future production or testing cycles.</li><li>Maintain detailed records of product defects and manufacturing issues to help identify and eliminate recurring problems and to provide a clear paper trail for accountability and error reporting.</li><li>Notify supervisors or plant leadership of issues or defect reports to support informed decisions about manufacturing processes and practices.</li><li>Support process improvements throughout testing and quality assurance processes to enhance product quality and reliability.</li><li>Suggest improvements to address potential systemic problems discovered during quality control activities, ensuring products are produced consistently and defects or errors do not persist.</li><li>Participate in structured training by reviewing each testing bench in the laboratory environment to gain a general understanding of workflows.</li><li>Use a training booklet to document learnings, add notes, and capture key information communicated during training.</li><li>Shadow Technologists to understand the testing processes and context for the documentation being reviewed, ensuring accurate and informed quality control review.</li><li>Learn and use relevant computer applications to perform documentation review and quality control tasks effectively.</li><li>Complete competency assessments after the training period to demonstrate understanding of quality control review responsibilities.</li></ul>Essential Skills<ul><li>Experience reviewing documentation, including records, procedures, and forms, for quality and compliance.</li><li>Familiarity with laboratory environments and processes related to quality control and quality assurance.</li><li>At least 1 year of experience within quality control, quality assurance, laboratory operations, document control, chemistry, biology, or related fields.</li><li>Ability to conduct product tests and assessments in industrial or warehouse settings to verify specifications and functionality.</li><li>Strong skills in identifying product defects or potential issues and determining appropriate corrective actions.</li><li>Experience analyzing results from lab or usability tests to identify defects and prevent recurrence.</li><li>Proficiency in maintaining detailed records of product defects and manufacturing issues for traceability and accountability.</li><li>Knowledge of standard operating procedures (SOPs) and Good Manufacturing Practices (GMP).</li><li>Strong data entry skills and attention to detail in documentation and recordkeeping.</li><li>Ability to support and participate in Quality Systems Compliance activities and Management Review meetings.</li><li>Effective communication skills to report issues and collaborate with supervisors and cross-functional teams.</li><li>Associate's degree in a scientific discipline or related field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s or Associate’s degree within a scientific discipline such as chemistry, biology, or a related field.</li><li>Preferred one or more years of Quality Assurance or Quality Control experience in a regulated environment.</li><li>Experience working in a clean and regulated environment.</li><li>Familiarity with quality or compliance-related projects and continuous improvement initiatives.</li><li>Comfort working with multiple departments and areas within a large laboratory setting.</li><li>Ability to learn and use computer applications specific to quality control and documentation review.</li><li>Willingness to participate in structured training programs, including bench-by-bench exposure and competency assessments.</li><li>Strong organizational skills and the ability to manage multiple tasks and documentation streams.</li></ul>Work EnvironmentThis role operates primarily in a laboratory environment focused on quality control review, with no direct testing performed by the specialist. The position also supports product assessments in industrial or warehouse settings and on the production floor. The environment is clean, regulated, and technology-driven, with a large laboratory that includes many departments and opportunities for cross-functional exposure and growth. Training takes place Monday through Friday from 11:00 a.m. to 7:30 p.m., and the regular work schedule runs Wednesday through Saturday from 10:00 p.m. to 8:30 a.m. New employees receive structured training, including exposure to one testing bench at a time, use of a training booklet for notes and reference, shadowing of Technologists to understand testing workflows, and learning relevant computer applications. A competency assessment occurs after approximately three weeks. The company culture is friendly and supportive, offering a clean, regulated setting with a long-term career path, opportunities for permanent conversion, and room for professional development within a large laboratory environment.Job Type &amp; LocationThis is a Contract position based out of NORCROSS, GA.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in NORCROSS,GA.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control TechnicianJob DescriptionWe are seeking a dedicated Quality Control Technician to ensure the quality of in-process and finished products for powder coatings. The role involves running various tests, including spray panels, gloss checks, and color testing, as well as conducting root cause analysis and making recommendations for product corrections. You will confirm product quality for final release and have the authority to halt production when nonconformance is detected. All test results will be entered into the SAP system.Responsibilities<ul><li>Perform quality control tests for in-process and finished products.</li><li>Conduct spray panel tests, gloss checks, and color tests.</li><li>Perform root cause analysis and recommend corrections for out-of-spec products.</li><li>Confirm the quality of finished products for final release.</li><li>Exercise stop authority when nonconformance is detected.</li><li>Enter test results into the SAP system.</li></ul>Essential Skills<ul><li>1 year of previous quality control experience.</li><li>Experience in paints, coatings, inks, or similar industries is preferred.</li><li>High school diploma or equivalent.</li><li>Proficiency in Microsoft Office.</li><li>Ability to make decisions and take ownership of quality control processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>1+ years of experience in powder coating with a background in quality testing is nice to have.</li><li>Bachelor's degree is preferred.</li><li>Experience from the food or pharmaceutical industry is considered.</li><li>Familiarity with SAP is a plus.</li></ul>Work EnvironmentThe position is based in the Quality Control office, with frequent visits to the production area to collect samples. The role operates on a 12-hour rotating shift (6:00 am – 6:00 pm) with a training period on the first shift (6:00 am – 2:30 pm) lasting 4-12 weeks. A casual dress code is observed, with a lab coat provided. The work environment requires comfort in a powder environment, and proficiency in English is necessary. An onsite interview is required.Job Type &amp; LocationThis is a Contract to Hire position based out of Geneva, IL.Pay and BenefitsThe pay range for this position is $23.64 - $24.64/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Geneva,IL.Application DeadlineThis position is anticipated to close on Jul 23, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Technician

Job Title: Quality Control TechnicianJob DescriptionThe Quality Control Technician prepares metal samples for detailed analysis, performs functional testing, and supports laboratory quality control activities to ensure consistent copper product quality. This role works closely with Quality, Production, and R&amp;D teams, follows established analytical procedures, and maintains accurate documentation while handling hazardous materials safely in a hands-on, lab-based environment.Responsibilities<ul><li>Prepare metal samples for scanning electron microscopy (SEM) and optical analysis, including cross-sectioning, potting, sanding, paste transfer, polishing, and other surface preparation techniques.</li><li>Perform functional testing such as International Annealed Copper Standard (IACS) measurements and thermal conductivity testing as needed.</li><li>Follow written analytical procedures and standard operating procedures to ensure accurate and repeatable test results.</li><li>Validate established test methods and assist in troubleshooting testing procedures to ensure consistent copper product quality.</li><li>Collect, enter, review, and validate test data in WinLIMS or similar data management systems.</li><li>Perform calculations based on test results and submit data and reports for review and approval.</li><li>Communicate sample status, test progress, and final results clearly and promptly to Quality, Production, and R&amp;D teams.</li><li>Maintain accurate and complete laboratory documentation, including SOPs, test methods, protocols, deviations, batch records, and Certificates of Analysis (COAs).</li><li>Handle hazardous materials safely, including proper labeling, storage, and disposal, in compliance with site safety and chemical hygiene protocols.</li><li>Adhere to all laboratory safety guidelines and contribute to a safe working environment.</li><li>Troubleshoot basic process and testing issues and escalate complex problems appropriately.</li><li>Work hands-on with metal components and assemblies that will be integrated into printed circuit board (PCB) products.</li><li>Manage time effectively to handle multiple tests, sample preparations, and documentation tasks within required timelines.</li><li>Support continuous improvement of laboratory processes, documentation practices, and quality control procedures.</li></ul>Essential Skills<ul><li>Experience in materials testing, experience working with metals, quality control experience, or laboratory experience (including academic lab experience).</li><li>Basic computer skills, including the ability to use Microsoft Excel, Word, and PowerPoint.</li><li>Ability to log and track process and test data accurately in electronic systems.</li><li>Ability to work effectively in a team environment and collaborate with cross-functional groups.</li><li>Ability to follow detailed instructions and written analytical procedures consistently.</li><li>Strong verbal and written communication skills to convey test status and results clearly.</li><li>Hands-on aptitude and comfort working with tools and equipment for sample preparation.</li><li>Good time management skills to prioritize tasks and meet testing deadlines.</li><li>Strong attention to detail with a focus on process control, documentation accuracy, and maintaining high quality standards.</li><li>Physical ability to stand, reach, and use fine tools for extended periods.</li><li>Ability to occasionally lift small weights and handle metal assemblies safely.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with statistical analysis software such as Minitab is a plus.</li><li>Experience using laboratory information management systems (LIMS), such as WinLIMS, is beneficial.</li><li>Exposure to working with metal materials that are used in printed circuit board (PCB) applications is advantageous.</li><li>Experience preparing samples for SEM or optical microscopy is an asset.</li><li>Prior experience in a manufacturing, quality control, or R&amp;D laboratory environment is preferred.</li></ul>Work EnvironmentThis role is based in a laboratory and production-support environment that focuses on metal materials used in components for printed circuit boards. The position is hands-on and physically active, involving frequent standing, reaching, and the use of fine tools for sanding, paste transfer, polishing, cross-sectioning, and other sample preparation tasks. The technician works with hazardous materials and chemicals and follows strict site safety and chemical hygiene protocols, including proper handling, storage, and disposal procedures. Work is performed using laboratory equipment for SEM and optical analysis, functional test instruments for IACS and thermal conductivity, and computer systems with software such as Microsoft Excel, Word, PowerPoint, WinLIMS, and potentially statistical tools like Minitab. The environment emphasizes teamwork and collaboration with Quality, Production, and R&amp;D teams, as well as careful adherence to documentation standards, process control, and quality requirements.Job Type &amp; LocationThis is a Contract position based out of Fremont, CA.Pay and BenefitsThe pay range for this position is $33.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Fremont,CA.Application DeadlineThis position is anticipated to close on Jul 24, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2 style="text-align:center;">Job Title: Quality Control Technician</h2>Job DescriptionThe Quality Control Technician supports the manufacturing and assembly of advanced fuel cell components by performing inspections, testing, and documentation to ensure products meet internal quality standards and regulatory requirements. This role works closely with manufacturing, engineering, and quality teams to drive continuous improvement and maintain high reliability in production. The technician contributes directly to product quality and performance while helping build innovative clean-energy technology within a growing advanced manufacturing team.Responsibilities<ul><li>Perform incoming, in-process, and final inspections of components and assemblies to ensure they meet specified requirements.</li><li>Conduct visual, dimensional, and functional inspections using hand tools and measurement equipment such as calipers, micrometers, and gauges.</li><li>Record inspection results accurately and maintain complete quality documentation and inspection reports in accordance with company procedures.</li><li>Identify non-conforming materials and products and support root cause investigations and corrective actions to prevent recurrence.</li><li>Support quality audits and compliance activities as required by internal quality systems and external standards.</li><li>Assist with maintaining quality records and databases to ensure traceability and compliance with quality systems.</li><li>Communicate inspection results, quality issues, and potential risks clearly to manufacturing and engineering teams.</li><li>Follow all safety, quality, and manufacturing procedures and guidelines while performing daily tasks.</li><li>Collaborate with cross-functional teams to support continuous improvement initiatives in production and quality processes.</li></ul>Essential Skills<ul><li>1–3+ years of experience in a quality control, inspection, or manufacturing technician role.</li><li>Proven ability to perform quality inspections on components and assemblies in a manufacturing environment.</li><li>Ability to read and interpret engineering drawings, work instructions, and specifications.</li><li>Hands-on experience with electrical, mechanical, or electro-mechanical assemblies.</li><li>Experience using basic inspection and measurement tools, including calipers, micrometers, and gauges.</li><li>Strong attention to detail and a high level of accuracy in documentation and recordkeeping.</li><li>Basic computer skills, including use of Microsoft Office and quality databases or ERP systems.</li><li>Ability to work effectively in a manufacturing or laboratory environment while following established procedures.</li><li>Strong communication skills to convey inspection results and quality issues to cross-functional teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working with advanced manufacturing or clean-energy technologies.</li><li>Familiarity with quality systems, audits, and compliance activities.</li><li>Interest in contributing to continuous improvement and high-reliability production.</li><li>Ability to collaborate with manufacturing, engineering, and quality teams in a fast-paced environment.</li></ul>Work EnvironmentThis role is based in a manufacturing and laboratory environment where the Quality Control Technician works closely with production and engineering teams around advanced fuel cell components. The position follows a Monday through Friday schedule, typically from 8:00 a.m. to 4:30 p.m. The environment involves working around electrical, mechanical, and electro-mechanical assemblies, using hand tools and measurement equipment such as calipers, micrometers, and gauges. Work is performed in accordance with established safety, quality, and manufacturing procedures, with regular use of computers for documentation, quality databases, and ERP systems. The setting supports innovative clean-energy technology development and offers the opportunity to be part of a growing advanced manufacturing team.Job Type &amp; LocationThis is a Permanent position based out of Mount Pleasant, PA.Pay and BenefitsThe pay range for this position is $47840.00 - $47840.00/yr.100% employee-paid health insurance coverage
Dental insurance
Vision insuranceWorkplace TypeThis is a fully onsite position in Mount Pleasant,PA.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control TechnicianJob DescriptionThis role focuses on evaluating color quality for textiles in a laboratory environment. The Quality Control Technician assesses production samples, establishes color tolerances, and makes approval or rejection decisions based on predefined color standards for pre-approved products. The technician works closely with the quality control lab team and uses both visual assessment and benchtop spectrophotometer measurements to ensure that all products meet strict color quality requirements.Responsibilities<ul><li>Receive and gather production samples for color evaluation in a timely and organized manner.</li><li>Perform visual assessments of textile samples to determine whether they meet pre-approved color standards and tolerances.</li><li>Establish and apply appropriate color tolerances when evaluating production lots.</li><li>Make clear pass or fail decisions on production lots based on color quality and adherence to standards.</li><li>Articulate and communicate color decisions, including the reasons for approvals or rejections, to relevant stakeholders.</li><li>Maintain accurate records of all evaluations and decisions, ensuring traceability and compliance with quality procedures.</li><li>Input comments, results, and evaluation details into Excel spreadsheets and other data entry systems.</li><li>Work alongside the quality control laboratory team using a benchtop spectrophotometer to confirm that quality control requirements are achieved.</li><li>Collaborate and communicate effectively with other lab technicians and quality control inspectors to support consistent color quality.</li><li>Support continuous improvement of color evaluation processes by providing feedback and observations from daily lab work.</li></ul>Essential Skills<ul><li>Strong color acuity and the ability to distinguish subtle differences in color.</li><li>Ability to pass the Farnsworth-Munsell 100 Hue Test with a superior rating (score less than 16).</li><li>Comfort working in a laboratory environment with textiles and color evaluation equipment.</li><li>Basic proficiency in Microsoft Excel, including entering and updating data accurately.</li><li>Superior written and verbal communication skills for documenting and explaining color decisions.</li><li>Experience or familiarity with quality control and inspection processes.</li><li>Attention to detail and accuracy when performing visual assessments and recording results.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in a quality control laboratory environment.</li><li>Familiarity with benchtop spectrophotometers or other color measurement instruments.</li><li>Experience or coursework in chemistry, textiles, or related laboratory sciences.</li><li>Experience with Excel data entry, including maintaining organized and accurate records.</li><li>Strong interpersonal skills and the ability to work collaboratively with lab technicians and inspectors.</li><li>Interest in color science, textiles, or niche industries related to color and materials.</li></ul>Work Environment<ul><li>This position is based in a laboratory environment focused on color evaluation for textiles. </li><li>The role operates on a first-shift schedule, typically from 7:00 a.m. to 3:30 p.m. </li><li>The technician works closely with other lab technicians and quality control inspectors, using tools such as a benchtop spectrophotometer and Excel-based data entry systems. </li><li>The work environment is described as very friendly and kind, with a strong sense of community and collaboration. </li><li>The organization operates within a highly specialized niche in the color and textiles industry and offers opportunities for professional growth and movement into other roles within the company. </li><li>Attire is consistent with standard laboratory settings, supporting safety, professionalism, and comfort during daily lab activities.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Carlstadt, NJ.Pay and BenefitsThe pay range for this position is $20.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Carlstadt,NJ.Application DeadlineThis position is anticipated to close on Jul 27, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control Technician Job DescriptionThe Quality Control Technician will actively monitor the production process to ensure compliance with food safety, food quality, and food defense requirements during processing, packing, and packaging. This position reports to the Quality Assurance Supervisor.Responsibilities<ul><li>Perform regular checks to ensure monitoring guidelines are followed during product processing.</li><li>Inspect finished products against predetermined standards and determine acceptance or rejection.</li><li>Perform biophysical testing on products, including viscosity, pH, water activity, moisture, and other quality measurements.</li><li>Monitor temperatures of refrigerated rooms, freezers, and sensitive ingredients.</li><li>Calibrate thermometers, scales, and other measuring equipment.</li><li>Monitor and verify proper operation of metal detectors.</li><li>Review production documentation for accuracy and completeness.</li><li>Monitor compliance with pre-operational requirements and Good Manufacturing Practices (GMPs).</li><li>Collect and maintain retention samples during production runs.</li><li>Participate in the frozen retention sample program.</li><li>Compile and distribute daily quality control paperwork.</li><li>Assist the QC Supervisor with GMP audits.</li><li>Maintain organization and cleanliness of QC work areas.</li><li>Support evaluation of raw materials and sample preparation activities.</li><li>Maintain effective communication with cross-functional plant teams.</li><li>Provide backup support for the QA Analyst as needed.</li><li>Perform additional duties as assigned by the QA Supervisor.</li></ul>Essential Skills<ul><li>Experience in food safety, quality control, and inspection.</li><li>Proficiency with Microsoft Office and data entry.</li><li>Strong written and communication skills.</li><li>Laboratory experience including pH and water testing, and viscosity testing.</li><li>SQF and Quality Control knowledge.</li></ul>Additional Skills &amp; Qualifications<ul><li>Minimum 1 year of experience in food manufacturing, baking experience preferred.</li><li>At least 6 months of quality assurance experience preferred.</li><li>ServSafe, HACCP, Baking Science, or similar certifications preferred.</li><li>High school diploma required; Associate degree or higher preferred.</li><li>Strong basic math and problem-solving abilities.</li><li>Ability to stand for extended periods.</li><li>Ability to lift up to 50 pounds.</li><li>Availability to work up to 7 days per week as needed.</li><li>Flexibility to work various shifts.</li></ul>Work EnvironmentThe role is based in a food manufacturing plant that exudes a variety of aromas, resembling a delicious bakery.Job Type &amp; LocationThis is a Contract to Hire position based out of Halethorpe, MD.Pay and BenefitsThe pay range for this position is $18.00 - $20.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Halethorpe,MD.Application DeadlineThis position is anticipated to close on Jul 29, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control Technician Job DescriptionThe Quality Control Technician actively monitors the production process to ensure products consistently meet food safety, food quality, and food defense requirements during processing, packing, and packaging. Reporting to the Quality Assurance Supervisor, this role performs hands-on testing, inspection, and documentation to verify that all products and processes comply with established standards and regulatory expectations.Responsibilities<ul><li>Perform regular checks throughout product processing to ensure all monitoring guidelines and procedures are followed.</li><li>Inspect finished products against predetermined quality standards and determine acceptance or rejection based on results.</li><li>Conduct biophysical testing on products, including viscosity, pH, water activity, moisture, and other quality measurements.</li><li>Monitor and record temperatures of refrigerated rooms, freezers, and temperature-sensitive ingredients.</li><li>Calibrate thermometers, scales, and other measuring and testing equipment to maintain accuracy.</li><li>Monitor and verify the proper operation and performance of metal detectors on production lines.</li><li>Review production documentation for accuracy, completeness, and compliance with quality requirements.</li><li>Monitor compliance with pre-operational requirements and Good Manufacturing Practices (GMPs) on the production floor.</li><li>Collect, label, and maintain retention samples during production runs in accordance with company procedures.</li><li>Participate in the frozen retention sample program, ensuring proper storage, handling, and documentation.</li><li>Compile, organize, and distribute daily quality control paperwork and reports.</li><li>Assist the Quality Control Supervisor with GMP audits and related documentation.</li><li>Maintain organization, cleanliness, and orderliness of quality control work areas and equipment.</li><li>Support the evaluation of raw materials and assist with sample preparation activities for testing and analysis.</li><li>Maintain effective communication with cross-functional plant teams to address quality issues and support continuous improvement.</li><li>Provide backup support for the QA Analyst as needed, including data entry and reporting tasks.</li><li>Perform additional duties as assigned by the QA Supervisor to support the overall quality and food safety program.</li></ul>Essential Skills<ul><li>Minimum 1 year of experience in food manufacturing; baking experience preferred.</li><li>At least 6 months of quality assurance or quality control experience preferred.</li><li>High school diploma required.</li><li>Strong basic math skills for measurements, calculations, and data interpretation.</li><li>Solid problem-solving abilities to identify, analyze, and resolve quality issues.</li><li>Ability to use Microsoft Office applications for data entry, documentation, and reporting.</li><li>Strong written and verbal communication skills for clear documentation and collaboration.</li><li>Experience or familiarity with food safety, quality control, and inspection practices.</li><li>Ability to perform laboratory-style testing, including pH, water testing, and viscosity testing.</li><li>Ability to stand for extended periods during shifts.</li><li>Ability to lift up to 50 pounds safely and repeatedly as needed.</li><li>Availability to work up to 7 days per week as business needs require.</li><li>Flexibility to work various shifts, including different hours and schedules.</li><li>Attention to detail and accuracy in inspection, testing, and documentation.</li><li>Comfort working in a fast-paced food manufacturing environment with strict quality standards.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree or higher in a related field preferred.</li><li>ServSafe, HACCP, Baking Science, SQF, or similar food safety and quality certifications preferred.</li><li>Experience with SQF or other recognized food safety and quality management systems.</li><li>Previous experience in a bakery or baked goods production environment.</li><li>Experience with data entry and documentation in a quality control or laboratory setting.</li><li>Familiarity with Good Manufacturing Practices (GMPs) and pre-operational inspections.</li><li>Ability to calibrate and troubleshoot measuring equipment such as thermometers, scales, and metal detectors.</li><li>Strong organizational skills to manage samples, paperwork, and multiple tasks simultaneously.</li></ul>Work EnvironmentThis role is based in a food manufacturing plant that produces baked goods for nationwide distribution. The facility operates in a fast-paced production environment with frequent exposure to the aromas and smells of a bakery. Team members work around industrial baking and packaging equipment, refrigerated rooms, freezers, and temperature-sensitive ingredients. The position requires standing for long periods, lifting up to 50 pounds, and working in varying temperatures. Shifts may vary, and availability up to 7 days per week may be required based on production demands. The environment emphasizes food safety, quality, and adherence to Good Manufacturing Practices, with regular use of laboratory testing equipment, measuring instruments, and computer systems for data entry and reporting.Job Type &amp; LocationThis is a Contract to Hire position based out of Halethorpe, MD.Pay and BenefitsThe pay range for this position is $18.00 - $20.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Halethorpe,MD.Application DeadlineThis position is anticipated to close on Jul 27, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2 style="text-align:center;">Biomedical Production Technician (Cleanroom)</h2>Job DescriptionThe Biomedical Production Technician works in a clean room manufacturing environment to help create biological medical devices derived from porcine liver. This role involves hands-on work with tissue samples, chemical solutions, and sterile processing in a regulated biotech setting. The technician spends most of the day on their feet and regularly lifts bins and livers weighing between 5 and 15 pounds. The position alternates between build weeks focused on production activities and non-build weeks focused on assembly, documentation, and facility upkeep, offering a consistent full-time schedule with opportunities for overtime and growth into higher-level technician roles.Responsibilities<ul><li>Work in a clean room manufacturing environment to support the production of biological medical devices derived from porcine liver.</li><li>Receive porcine livers and verify materials according to established procedures.</li><li>Trim porcine livers and prepare tissue samples for further processing.</li><li>Scoop, measure, and mix chemical solutions used in liver processing, following precise instructions and safety guidelines.</li><li>Perform decellularization of porcine livers in accordance with standard operating procedures (SOPs) and GMP requirements.</li><li>Create, cut, and prepare specific tissue pieces for use in medical devices, ensuring accuracy and consistency.</li><li>Sterilize and maintain the cleanliness of the clean room, including equipment and work surfaces, to meet sterile processing standards.</li><li>Follow SOPs and work instructions rigorously to ensure compliance with GMP and regulatory requirements.</li><li>During non-build weeks, perform assembly tasks related to device production and component preparation.</li><li>Sweep floors, clean work areas, and perform general housekeeping duties in the clean room and surrounding spaces as needed.</li><li>Update manufacturing records (MFR paperwork) and maintain accurate documentation of production activities.</li><li>Support administrative tasks such as order receiving and shipping-related activities as needed.</li><li>Collaborate with the R&amp;D team and other technicians to support production and development activities.</li><li>Work directly with porcine livers during production cycles and assist R&amp;D with porcine kidneys during downtime.</li><li>Maintain strong attention to detail in all aspects of work, including tissue handling, chemical mixing, documentation, and cleaning.</li><li>Adhere to safety protocols, aseptic techniques, and sterile processing practices to protect product quality and personal safety.</li><li>Contribute to a small, collaborative team environment and work independently when required to meet production timelines.</li></ul>Essential Skills<ul><li>Minimum of 6+ months of experience working within a clean room setting.</li><li>Associate degree in a medical or science-related field.</li><li>Experience following SOPs in a GMP-regulated environment.</li><li>Demonstrated strong attention to detail, verified through references or prior work experience.</li><li>Hands-on experience with cleanroom practices and sterile processing.</li><li>Ability to work with tissue samples, including trimming and handling biological materials.</li><li>Knowledge of aseptic technique and sterilization procedures.</li><li>Ability to safely mix and handle chemicals used in biological processing.</li><li>Comfort working on feet for the majority of the day and lifting 5–15 pound bins and tissue materials.</li><li>Capability to maintain accurate manufacturing documentation and follow regulated processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in a scientific field, such as biology, is preferred.</li></ul>Work EnvironmentThis role is based in a new biotech manufacturing facility in Plymouth, MN, where the clean room is being further built out and optimized. The technician joins a small team of three technicians who partner closely with the R&amp;D group, creating a collaborative environment with opportunities to learn and contribute across production and development activities. Work involves direct handling of porcine livers during production cycles and assisting with porcine kidneys during downtime, in a regulated, clean room setting that requires adherence to sterile processing and aseptic techniques. The production timeline runs from Monday through the following Tuesday, when finished product is shipped out. Production (build) weeks are typically 40+ hours, with mandatory overtime bringing total hours to approximately 42–44 hours. Non-build weeks are around 36 hours. Non-build week hours are generally 8:00 a.m. to 4:30 p.m., Monday through Friday. During build weeks, hours vary: Mondays run from 8:00 a.m. to 4:30 p.m.; Tuesdays through Thursdays start between 6:00 a.m. and 6:30 a.m. and end around 4:30–5:00 p.m.; Fridays start at 7:00 a.m. and typically finish around 1:00–2:00 p.m. The environment is regulated and structured, offering a consistent full-time schedule, some overtime, and the ability to work both independently and as part of a small, focused team in a clean room setting.Job Type &amp; LocationThis is a Contract to Hire position based out of plymouth, MN.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in plymouth,MN.Application DeadlineThis position is anticipated to close on Aug 5, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Technician – 2nd ShiftJob DescriptionThis Quality Control Technician role provides hands-on quality control support to the Quality Assurance and Regulatory Compliance functions within a chemical manufacturing facility that produces industrial cleaning supplies for a wide range of industries. Working primarily in a laboratory setting with regular time on the production floor, you perform routine testing on raw materials and finished products, support investigations into quality issues, and help ensure that all batches and packaging meet established specifications. This is a contract-to-hire, 2nd shift position offering broad exposure to lab techniques, production operations, root cause analysis, and direct interaction with production, R&amp;D, and customers.Responsibilities<ul><li>Perform basic laboratory tests on raw materials, in-process batches, and fill line samples, including pH, specific gravity, viscosity, and titrations.</li><li>Calculate and document batch adjustments as needed based on test results.</li><li>Inspect packaging lines to verify conformance to specifications for fill weight, cap torque, labels and label placement, lot coding, and related parameters.</li><li>Document all test and inspection results accurately on both paper and electronic forms.</li><li>Review and maintain production records and files to ensure completeness, accuracy, and traceability.</li><li>Inspect finished goods and received components to determine release status and compliance with quality standards.</li><li>Participate in investigations of quality complaints and nonconformances, including reviewing documentation, retesting product samples, and inspecting components.</li><li>Maintain strong attention to detail and professional integrity in all testing, documentation, and communication activities.</li><li>Communicate effectively with production staff and management to relay test results, quality concerns, and recommended actions.</li><li>Adapt to varying daily workloads, spending some days primarily in the lab and other days focused on inspections and activities in the plant, depending on production needs.</li><li>Contribute to root cause analysis efforts to resolve customer complaints and feedback by working backward from reported issues to identify and address underlying causes.</li><li>Apply short-term memory skills to manage multiple tests, inspections, and documentation tasks, ensuring that critical information is retained and recorded accurately.</li></ul>Essential Skills<ul><li>Ability to perform basic laboratory tests such as pH measurement, specific gravity, viscosity, and titrations.</li><li>Capability to calculate batch adjustments based on laboratory data and established specifications.</li><li>Experience or aptitude in quality control, quality assurance, or laboratory work in a manufacturing or industrial environment.</li><li>Strong attention to detail and commitment to maintaining professional integrity in all aspects of work.</li><li>Ability to read, edit, proofread, and interpret technical documents such as Safety Data Sheets (SDS), Standard Operating Procedures (SOP), and product labeling.</li><li>Proficiency in grammar and spelling to ensure clear and accurate documentation.</li><li>Effective communication skills to interact with production staff, management, R&amp;D, and customers.</li><li>Comfort working in both laboratory and industrial plant environments and interacting with a variety of people.</li><li>Good short-term memory to manage multiple tasks and retain important information not always documented immediately.</li><li>Computer proficiency using Windows, Word, Excel, and Outlook.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Jul 27, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control TechnicianJob DescriptionThe Quality Control Technician performs hands-on quality control testing on the production floor in a food manufacturing environment. This role conducts routine inspections and audits on multiple production lines, verifies product quality through a variety of tests, and documents all results accurately in both paper and electronic formats. The technician collaborates closely with production staff to identify issues, correct errors, and help ensure that all products meet established food safety and quality standards.Responsibilities<ul><li>Perform quality control testing on the production floor, including metal detection checks, leak tests, percentage tests, and other routine inspections.</li><li>Conduct hourly line audits on each production line, including first-piece inspections, in-process checks, and final inspections or quality control tests.</li><li>Carry out basic laboratory testing such as moisture, salt, and fat analysis using automated testing equipment.</li><li>Perform calculations to determine percentages of materials and total ounces for products and ingredients.</li><li>Accurately document daily test results, production numbers, and quality checks in both paper logs and computer systems.</li><li>Work closely with production personnel each day to perform quality control checks and assist in correcting errors or nonconformances that may occur.</li><li>Apply food quality and quality assurance principles, including HACCP and GMP practices, during all inspections and testing activities.</li><li>Support line audits and quality reviews to verify compliance with internal standards and customer requirements.</li><li>Participate in cross-training across all aspects of the quality department, performing both lab-based testing and on-floor quality checks as needed.</li><li>Maintain a clean, organized, and compliant work area in accordance with food manufacturing and quality guidelines.</li></ul>Essential Skills<ul><li>Minimum of 1 year of food quality control experience, including exposure to HACCP processes.</li><li>Understanding of quality control processes in a manufacturing environment.</li><li>Understanding of food quality processes and standards.</li><li>Ability to perform basic math calculations using a calculator, including percentage calculations (for example, calculating 60% of 12 ounces).</li><li>Familiarity with quality assurance concepts such as GMP, line audits, and QC testing.</li><li>Ability to document data accurately in both paper and computer-based systems.</li><li>Strong attention to detail and commitment to maintaining high quality and food safety standards.</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma, HSED, or GED.</li><li>Experience working with HACCP and GMP in a food manufacturing environment.</li><li>Comfort working with automated testing equipment for moisture, salt, and fat analysis.</li><li>Ability to collaborate effectively with production personnel and other departments.</li><li>Willingness to be cross-trained in all aspects of the quality department and to perform a variety of quality-related tasks as needed.</li><li>Interest in professional growth within a growing business that offers opportunities for advancement.</li></ul>Work EnvironmentThe role is based in a smaller food manufacturing facility that produces large volumes of product for major retail customers and is expanding to serve additional large clients. The company operates a growing operation with a new pasteurization facility that supports increased production and creates opportunities for advancement. The schedule is primarily Monday through Friday, with occasional weekend work during the busy season. The Quality Control Technician works in both production and laboratory settings and will be cross-trained across the quality department, meaning some days may involve no lab work and other days may be entirely lab-focused. The environment emphasizes stable hours, year-over-year business growth, and the potential for upward promotion. The facility uses automated testing equipment and standard food manufacturing technologies, and offers good benefits including health, dental, and vision coverage.Job Type &amp; LocationThis is a Permanent position based out of WAUKESHA, WI.Pay and BenefitsThe pay range for this position is $41600.00 - $45760.00/yr.$1500 sign on bonus (paid incrementally)Workplace TypeThis is a fully onsite position in WAUKESHA,WI.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control TechnicianJob DescriptionThe Quality Control Technician supports consistent product quality and safety on the production floor of a food manufacturing facility. This role performs routine and specialized quality checks, conducts line audits, completes basic laboratory tests, and accurately documents all results. The technician collaborates closely with production teams to identify and correct issues in real time, helping to maintain compliance with food quality standards and customer specifications.Responsibilities<ul><li>Perform quality control testing on the production floor, including metal detection checks, leak tests, percentage tests, and other in-process inspections.</li><li>Conduct hourly line audits on each production line, including first-piece, in-process, and final inspections and quality control tests.</li><li>Perform calculations to determine percentages of materials and total ounces to verify product specifications and formulations.</li><li>Complete basic automated testing for key product attributes such as moisture, salt, and fat content.</li><li>Accurately document daily production and testing data in both paper and computer systems, ensuring records are complete, legible, and organized.</li><li>Work closely with production personnel on a daily basis to perform quality control checks and help identify, communicate, and correct errors or deviations from standards.</li><li>Follow established quality control and food quality processes, including Good Manufacturing Practices (GMP) and HACCP procedures, to maintain product safety and consistency.</li><li>Support cross-training efforts by learning and performing a variety of tasks within the quality department, including both lab-based and floor-based quality activities as needed.</li></ul>Essential Skills<ul><li>Understanding of quality control processes in a manufacturing environment.</li><li>Understanding of food quality processes and standards, including practical application in a production setting.</li><li>Knowledge of Good Manufacturing Practices (GMP) as they relate to food production and quality control.</li><li>Ability to perform basic math calculations using a calculator, including percentage calculations (for example, determining that 60% of 12 ounces equals 7.2 ounces).</li><li>At least 1 year of food quality control experience, including experience with HACCP.</li><li>High school diploma, HSED, or GED.</li><li>Ability to perform routine quality checks such as line audits, percentage checks, and basic QC tests accurately and consistently.</li><li>Ability to use computer systems for data entry and documentation of testing and production information.</li><li>Attention to detail and accuracy in both testing and documentation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with quality assurance or quality control in a food manufacturing environment.</li><li>Familiarity with line audit procedures and documenting quality findings.</li><li>Comfort working with automated testing equipment for moisture, salt, and fat analysis.</li><li>Strong communication skills to collaborate effectively with production personnel and other team members.</li><li>Willingness to be cross-trained in all aspects of the quality department and to perform a variety of quality tasks as needed.</li><li>Interest in professional growth and advancement within a growing business that offers opportunities for promotion.</li></ul>Work EnvironmentThis role is based in a smaller food manufacturing company that produces high volumes of product for major retail customers and is actively growing by adding new large accounts. The work is performed in a production and lab environment where the technician spends time both on the production floor and in the quality lab, depending on daily needs. The schedule is Monday through Friday, with occasional weekend work during the busy season. The position offers a stable business environment with consistent hours, yearly pay raises, and opportunities for advancement as the company expands, including new facilities that support growth in production and quality operations. The employer provides a comprehensive benefits package, including health, dental, and vision coverage. The technician is cross-trained across the quality department, so some days may involve no lab work while other days may be entirely lab-based, and the role requires flexibility and openness to performing any assigned quality-related tasks.Job Type &amp; LocationThis is a Permanent position based out of WAUKESHA, WI.Pay and BenefitsThe pay range for this position is $41600.00 - $45760.00/yr.$1,500 sign on bonus that is paid incrementallyWorkplace TypeThis is a fully onsite position in WAUKESHA,WI.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Control Technician II Job DescriptionThe Quality Control Technician II plays a key role in ensuring product quality and food safety by performing all Quality Control Technician I duties and additional verification, calibration, and product quality assessments. This position supports quality assurance programs, contributes to continuous improvement of processes, and helps maintain compliance with Good Manufacturing Practices and established procedures in a food production environment.Responsibilities<ul><li>Perform all Quality Control Technician I responsibilities, including routine quality checks and documentation.</li><li>Conduct product temperature checks throughout production to ensure compliance with specifications.</li><li>Perform ATP equipment hygiene checks to verify sanitation effectiveness.</li><li>Inspect production equipment for cleanliness and sanitation readiness prior to use.</li><li>Carry out Good Manufacturing Practice (GMP) inspections on the production floor.</li><li>Verify sanitizer concentration levels to confirm proper cleaning and disinfection.</li><li>Measure pH and salt concentrations to ensure products meet defined quality standards.</li><li>Perform pre-operational inspections on equipment prior to production start-up.</li><li>Verify water temperatures to ensure they meet process and safety requirements.</li><li>Accurately document all test results and promptly report deviations to quality assurance leadership.</li><li>Conduct thermometer calibrations to maintain accurate temperature measurement instruments.</li><li>Perform seal integrity checks using vacuum testing equipment to confirm proper package sealing.</li><li>Collect sensory and retain samples for ongoing quality monitoring and traceability.</li><li>Conduct sensory evaluations of finished products to assess quality attributes such as appearance, texture, and flavor.</li><li>Verify label accuracy and compliance, including product information, coding, and regulatory requirements.</li><li>Communicate food safety and product quality concerns to supervisors and production teams in a clear and timely manner.</li><li>Support quality assurance and quality control activities related to temperature checks, weight checks, CAPA (Corrective and Preventive Actions), SOP (Standard Operating Procedures) adherence, and pH concentration monitoring.</li><li>Assist with environmental swabbing and label inspections as part of broader quality control programs.</li><li>Participate in pre-operational inspections and environmental verification activities to help maintain a safe and compliant processing environment.</li></ul>Essential Skills<ul><li>Hands-on quality control experience in a food production or meat industry environment.</li><li>Ability to perform temperature checks, weight checks, and pH readings accurately and consistently.</li><li>Strong attention to detail when conducting inspections, measurements, and documentation.</li><li>Working knowledge of Good Manufacturing Practices (GMP) and standard operating procedures in a food processing setting.</li><li>Capability to conduct pre-operational inspections on equipment and production areas.</li><li>Experience with environmental swabbing and label inspections in ready-to-eat or similar production areas.</li><li>Basic computer skills for data entry, documentation, and use of quality management systems.</li><li>Ability to follow established quality assurance and food safety protocols, including CAPA and SOP requirements.</li><li>Effective communication skills to relay food safety and quality issues to supervisors and production staff.</li><li>Willingness and ability to work evening and overnight shifts as required by production schedules.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in the meat industry is strongly preferred.</li><li>Familiarity with quality assurance processes, including CAPA and SOP development or adherence.</li><li>Comfort using measurement and testing equipment such as thermometers, vacuum testing devices, and pH meters.</li><li>Bachelor’s degree in Food Science or a related field is helpful and considered an asset.</li><li>Ability to train on earlier shifts (such as afternoon start times) before transitioning to a third shift schedule.</li><li>Strong organizational skills and the ability to manage multiple checks and inspections during a production run.</li><li>Analytical mindset for interpreting test results and contributing to root cause investigations and corrective actions.</li><li>Reliability and consistency in following documented procedures and maintaining accurate records.</li></ul>Work EnvironmentThis role is based in a food production facility with a focus on meat processing and ready-to-eat products. You work closely with production, sanitation, and quality assurance teams while performing inspections, measurements, and environmental verifications on the floor. The position follows a Sunday–Thursday schedule, primarily on third shift from 8:00 PM to 4:30 AM, with training initially conducted on earlier shifts such as 2:00 PM or 4:00 PM before transitioning to the night schedule. The environment involves working in processing areas, coolers, and freezers, handling testing equipment for temperature, pH, weight, and seal integrity checks. Standard facility attire and appropriate food safety and sanitation gear are required. The role offers an opportunity for long-term growth following an initial six-month contract period, with exposure to quality systems, audits, and continuous improvement initiatives in a structured and safety-focused setting.Job Type &amp; LocationThis is a Contract to Hire position based out of Carson, CA.Pay and BenefitsThe pay range for this position is $23.70 - $24.57/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Carson,CA.Application DeadlineThis position is anticipated to close on Jul 27, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Control Technician II

Job Title: Quality Engineer Job DescriptionThe Quality Engineer supports customers by managing quality concerns, implementing corrective actions, and driving continuous improvement across manufacturing operations. This role uses Advanced Product Quality Planning (APQP) processes and root cause analysis to identify issues, develop sustainable solutions, and ensure products consistently meet quality, cost, and customer expectations.Responsibilities<ul><li>Support customers by addressing quality concerns, coordinating responses, and ensuring timely and effective resolution.</li><li>Utilize APQP processes to plan, monitor, and improve product and process quality throughout the manufacturing lifecycle.</li><li>Lead and participate in corrective action audits and cross-functional problem-solving teams to support continuous improvement and meet performance criteria.</li><li>Understand, communicate, and train operational personnel on customer-specific requirements to ensure compliance and consistency.</li><li>Perform process capability and measurement studies using appropriate statistical techniques to evaluate and improve process performance.</li><li>Document manufacturing processes and implement continuous improvement actions to support quality, cost efficiency, and customer satisfaction.</li><li>Learn and interpret customer-specific quality system requirements and ensure they are integrated into internal processes and procedures.</li><li>Act as a liaison with external parties, including customers, on matters related to program and quality requirements.</li><li>Read and interpret Geometric Dimensioning and Tolerancing (GD&amp;T) and direct dimensional layouts, and coordinate testing and timing as needed.</li><li>Participate in quality investigations to determine root causes, define corrective and preventive actions, and verify their effectiveness.</li><li>Support and contribute to the development and maintenance of the quality management system and related documentation.</li><li>Conduct or support audits related to quality systems, processes, and products to ensure ongoing compliance and performance.</li></ul>Essential Skills<ul><li>2+ years of experience in manufacturing quality engineering.</li><li>Hands-on experience with APQP processes in a manufacturing environment.</li><li>Proficiency in root cause analysis and root cause failure analysis for quality issues.</li><li>Experience with PPAP (Production Part Approval Process) documentation and requirements.</li><li>Experience with PFMEA (Process Failure Mode and Effects Analysis).</li><li>Knowledge of quality engineering principles and practices in a production setting.</li><li>Experience working within a quality management system and quality management processes.</li><li>Ability to perform process capability and measurement studies using statistical techniques.</li><li>Ability to read and interpret GD&amp;T and dimensional layouts.</li><li>Strong skills in conducting and supporting audits related to quality.</li><li>Associate’s or Bachelor’s degree.</li></ul>Additional Skills &amp; Qualifications<ul><li>Automotive manufacturing experience (preferred).</li><li>Experience with injection molding processes (preferred).</li><li>Experience with plating operations (preferred).</li><li>Experience with assembly operations (preferred).</li><li>Demonstrated ability to train and coach operational personnel on customer-specific requirements.</li><li>Strong communication skills to effectively liaise with customers and internal teams.</li><li>Self-starter with high initiative, especially in environments with limited on-site technical support.</li><li>Ability to work effectively in a fast-paced environment and contribute to building and strengthening the engineering team.</li><li>Interest in continuous improvement and willingness to support and lead problem-solving initiatives.</li></ul>Work EnvironmentThe work environment includes injection molding and plating lines, where some areas can be hot and dirty due to the nature of the processes. The role is based at a site with limited technical support on-site, so the Quality Engineer must work independently and proactively. The environment is fast-paced, with opportunities to help build and develop the engineering team. The organization offers 6 paid holidays and 1 week of paid time off, reflecting a commitment to work-life balance and employee well-being.Job Type &amp; LocationThis is a Contract to Hire position based out of Nicholasville, KY.Pay and BenefitsThe pay range for this position is $35.00 - $47.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Nicholasville,KY.Application DeadlineThis position is anticipated to close on Jul 28, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Engineer

Job Title: Quality Engineer Job DescriptionThis Quality Engineer role serves as the primary quality representative for a newly established U.S. manufacturing facility, leading the development and implementation of plant-wide quality standards and procedures. The position focuses on driving robust quality systems, resolving customer issues, and partnering closely with production and engineering teams to improve product quality, reduce scrap, and enhance process capability. This role offers a clear pathway for career growth, with the opportunity to advance into a quality management or director-level position within a few years based on performance and contribution.Responsibilities<ul><li>Serve as the primary quality representative for the manufacturing facility and champion plant-wide quality standards and procedures.</li><li>Act as the main point of contact for customer quality concerns, ensuring timely investigation, communication, and resolution of issues.</li><li>Lead root cause analysis and corrective action activities related to customer complaints, internal nonconformances, and supplier quality issues.</li><li>Establish, monitor, and report key quality metrics, and drive continuous improvement initiatives based on data and trends.</li><li>Develop, maintain, and improve quality documentation, including control plans, inspection procedures, work instructions, and standard operating procedures.</li><li>Partner with production and engineering teams to improve product quality, reduce scrap, and increase process capability.</li><li>Support PFMEA, Process Flow Diagram, Control Plan development, and new process development activities.</li><li>Conduct process and quality system audits to ensure compliance with customer requirements and applicable quality standards.</li><li>Manage calibration programs, gauge control activities, and measurement system analysis (MSA) to ensure accuracy and reliability of measurement systems.</li><li>Collaborate with suppliers and global quality teams to ensure consistent quality standards and practices across operations.</li><li>Use tools such as Root Cause Analysis, 5 Why, Fishbone (Ishikawa), SPC, and MSA to solve problems and strengthen processes.</li><li>Prepare and support quality planning documentation, including PPAP submissions and related customer-required documentation.</li><li>Interpret engineering drawings and apply GD&amp;T principles to ensure product and process conformance.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering, Manufacturing Engineering, Industrial Engineering, Mechanical Engineering, or a related technical field.</li><li>1–3 years of experience in a manufacturing quality engineering role.</li><li>Basic understanding of quality management systems such as ISO 9001 and/or IATF.</li><li>Familiarity with Root Cause Analysis, 5 Why, Fishbone (Ishikawa), Control Plans, PFMEA, SPC, and MSA.</li><li>Experience supporting quality documentation and quality planning activities, including Control Plans and PPAP documentation.</li><li>Ability to interpret engineering drawings, with exposure to GD&amp;T concepts.</li><li>Proficiency with Microsoft Office, particularly Excel, for data analysis and reporting.</li><li>Strong analytical skills with the ability to interpret quality data and drive fact-based decisions.</li><li>Strong organizational skills with the ability to manage multiple tasks and priorities.</li><li>Effective written and verbal communication skills for interacting with customers, suppliers, and cross-functional teams.</li><li>Ability to work both independently and collaboratively in a team environment.</li><li>Experience in automotive, industrial, or high-volume manufacturing environments.</li><li>Experience with Lean Manufacturing and continuous improvement initiatives.</li><li>Experience using Statistical Process Control (SPC) to monitor and improve manufacturing processes.</li><li>Demonstrated experience conducting root cause analysis and implementing corrective actions.</li><li>Experience using quality data analysis software such as Minitab.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior experience supporting PPAP documentation and customer-facing quality planning activities is preferred.</li><li>Hands-on experience interpreting complex engineering drawings and applying GD&amp;T is preferred.</li><li>Exposure to high-volume or automotive-related manufacturing processes is highly beneficial.</li><li>Demonstrated ability to drive continuous improvement projects using Lean tools and methods.</li><li>Interest in growing into a leadership role, with potential advancement into quality manager or director responsibilities within 3–4 years based on performance.</li><li>Comfort working in a fast-paced, evolving manufacturing environment where quality systems are being built and refined.</li></ul>Work EnvironmentThis role is fully onsite in a manufacturing facility, with standard hours of approximately 7:00 a.m. to 4:30 p.m. and an expected workweek of around 45 hours. You will work closely with production, engineering, and global quality teams in a hands-on environment focused on high-volume manufacturing and continuous improvement. The facility operates with structured quality systems and uses tools such as SPC, MSA, PFMEA, and quality data analysis software like Minitab, alongside common productivity tools such as Microsoft Excel. The environment emphasizes collaboration, problem-solving, and data-driven decision-making, offering clear opportunities for professional growth and advancement in quality leadership.Job Type &amp; LocationThis is a Contract to Hire position based out of Fort Wayne, IN.Pay and BenefitsThe pay range for this position is $28.85 - $33.65/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Fort Wayne,IN.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThis Quality Engineer role focuses on driving continuous improvement in product quality and manufacturing processes within an aerospace environment. You will lead detailed analysis of customer returned parts, implement corrective and preventive actions, and supervise a final inspection team to ensure products meet stringent industry standards. The position also plays a key role in material review activities and validation of customer returns to enhance overall quality performance.Responsibilities<ul><li>Perform detailed analysis of customer returned parts and use the findings to drive corrective and preventive action (CAPA) improvements.</li><li>Prevent internal recurring failures and reduce risks by conducting thorough root cause analysis to identify and address existing issues.</li><li>Validate customer return material authorizations (RMAs) and define further actions to improve manufacturing processes and product quality.</li><li>Supervise a team of six in the final inspection department, providing day-to-day guidance, coaching, and training as needed.</li><li>Represent the quality assurance function on the material review board (MRB) for internal rejections and ensure appropriate disposition of nonconforming materials.</li><li>Prepare, review, and approve first article inspections (FAI) in accordance with AS9102 requirements for aerospace products.</li><li>Support and participate in internal and external audits, ensuring compliance with applicable quality standards and customer requirements.</li><li>Collaborate closely with cross-functional teams, including manufacturing and engineering, to implement effective corrective actions and process improvements.</li><li>Monitor quality metrics and trends, and recommend actions to enhance overall product reliability and customer satisfaction.</li></ul>Essential Skills<ul><li>Proven experience as a Quality Engineer in an aerospace or similarly regulated manufacturing environment.</li><li>Strong knowledge of AS9102 requirements and practical experience with first article inspections (FAI).</li><li>Demonstrated ability to perform root cause analysis and implement effective corrective and preventive actions (CAPA).</li><li>Hands-on experience with customer returned material analysis and validation of RMAs.</li><li>Experience participating in or supporting material review board (MRB) activities for internal rejections.</li><li>in auditing or supporting quality audits within a manufacturing or aerospace setting.</li><li>Ability to supervise and guide a final inspection team, including coaching and on-the-job training.</li><li>Strong analytical and problem-solving skills with a structured, data-driven approach.</li><li>Clear and effective communication skills for working with cross-functional teams and presenting findings.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working over a connector manufacturing line or similar product line.</li><li>Familiarity with aerospace quality systems and industry-specific documentation requirements.</li><li>Exposure to continuous improvement methodologies within a manufacturing environment.</li><li>Ability to document and report on quality issues, corrective actions, and inspection results in a clear and organized manner.</li></ul>Work EnvironmentThis role operates within an aerospace manufacturing and inspection environment, with a strong focus on quality assurance and compliance. You will work closely with final inspection, manufacturing, engineering, and material review teams, frequently engaging with customer return analysis and first article inspections under AS9102 standards. The position involves hands-on work with components on a connector line, participation in MRB activities, and involvement in audits and process improvement initiatives. The environment emphasizes structured processes, detailed documentation, and collaboration across departments to maintain high product quality and reliability.Job Type &amp; LocationThis is a Contract to Hire position based out of Glendale, CA.Pay and BenefitsThe pay range for this position is $36.06 - $36.06/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Glendale,CA.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Supplier Quality EngineerJob DescriptionThe Supplier Quality Engineer provides ongoing support to the business by driving supplier development and improvement activities aligned with corporate quality metrics. This role works closely with Materials/Purchasing, Sourcing, Branch Operations, and Quality Assurance teams to ensure suppliers meet stringent quality standards across multiple industries. The position focuses on auditing and developing suppliers, resolving customer concerns, and supporting new product introductions while maintaining robust quality systems and processes.Responsibilities<ul><li>Conduct comprehensive audits and evaluations for new and existing suppliers to ensure compliance with quality requirements.</li><li>Review and assess self-assessments submitted by potential suppliers and determine their suitability.</li><li>Visit supplier facilities to evaluate their quality systems, processes, and capabilities.</li><li>Complete formal supplier audits, document findings, and communicate results to relevant stakeholders.</li><li>Issue supplier corrective actions based on audit findings and performance issues, and follow up to ensure timely and effective closure.</li><li>Participate in customer audits of suppliers, representing the organization’s quality interests and ensuring supplier readiness.</li><li>Issue monthly supplier performance scorecards and communicate results to suppliers and internal teams.</li><li>Monitor supplier performance, identify trends, and determine areas for improvement in supply quality and delivery performance.</li><li>Perform on-site audits for poor-performing or critical suppliers and develop targeted improvement plans.</li><li>Develop and implement action plans to improve the quality performance of identified suppliers.</li><li>Review and approve Production Part Approval Process (PPAP) submissions when suppliers initiate changes.</li><li>Provide aging reports for quality rejections by branch, supplier, reason code, and associated costs.</li><li>Assist the Quality Assurance team in processing and resolving customer concerns in a timely and effective manner.</li><li>Provide technical support to the organization in new product introduction, ensuring quality requirements are defined and met.</li><li>Support operational excellence initiatives and contribute to continuous improvement in quality processes.</li><li>Apply appropriate quality assurance and improvement methodologies, including structured problem-solving tools.</li><li>Continuously upgrade personal skills and knowledge to improve effectiveness and stay current with industry practices.</li><li>Provide training and guidance to less experienced or less skilled personnel on quality tools, processes, and standards.</li><li>Work closely with key customers to understand issues at the plant level and develop effective solutions.</li><li>Engage directly with major customers in automotive and heavy truck sectors to address quality concerns and drive corrective actions.</li><li>Lead or support corrective action activities that may function as mini Six Sigma projects to address recurring issues.</li><li>Spend significant time on the shop floor and in the laboratory, investigating and resolving quality problems and issues.</li><li>Perform hands-on work in the lab using gauges, inspection tools, and testing equipment to validate product quality.</li><li>Visit domestic suppliers regularly, with travel typically ranging from approximately 10% to 20% depending on project needs.</li><li>Apply Advanced Product Quality Planning (APQP) frameworks and related tools such as PPAP, PFMEA, control plans, and GD&amp;T in supplier and product development activities.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience in quality engineering, supplier quality, or a closely related quality-focused role.</li><li>Bachelor’s degree in an engineering discipline.</li><li>Strong knowledge of ISO 9001:2015 quality standards and familiarity with IATF requirements.</li><li>Certification in auditing and demonstrated experience conducting quality system and process audits.</li><li>Proficiency in APQP and PPAP, including the ability to review, approve, and provide training on these processes to suppliers.</li><li>Hands-on experience with corrective action and continuous improvement processes, including 8D, 5 Why, and fishbone (Ishikawa) analysis.</li><li>Familiarity with various manufacturing processes and their impact on product quality.</li><li>Knowledge of material testing and evaluation procedures to assess product conformance.</li><li>Experience with gauging and inspection methods, including the use of precision measurement tools.</li><li>Ability to interpret and apply PFMEA, control plans, and GD&amp;T within supplier and product quality contexts.</li><li>Strong analytical and problem-solving skills with a structured approach to root cause analysis.</li><li>Effective communication skills to interact with suppliers, internal teams, and customers at multiple levels.</li><li>Ability to work hands-on in laboratory and shop-floor environments to investigate and resolve issues.</li><li>Willingness and ability to travel domestically approximately 10% to 20% of the time, depending on project demands.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to the automotive and/or heavy truck industry, including familiarity with sector-specific quality expectations.</li><li>Experience working with customers in industries such as aerospace, automotive, heavy equipment, electronics, and defense.</li><li>Experience with gage calibration and quality-related software tools.</li><li>Hands-on experience using Optical Comparators, Hardness Testers, and plug gages in a lab environment.</li><li>Exposure to lean methodologies and Six Sigma principles, including participation in improvement projects.</li><li>Experience with quality management systems and supplier process or product audits.</li><li>Ability to train suppliers and internal staff on APQP, PPAP, and other quality tools.</li><li>Strong customer-facing skills and experience working directly with key accounts to resolve plant-level issues.</li><li>Demonstrated ability to manage multiple projects and priorities while maintaining attention to detail.</li><li>Motivation to grow supplier quality expertise and work across a variety of industries and product types.</li></ul>Work EnvironmentThe role operates within a small office environment attached to a very clean and well-equipped quality laboratory. The lab includes instruments such as micrometers, calibrated gages, optical comparators, hardness testers, plug gages, and computer-based measurement and reporting systems. The broader facility includes a large warehouse focused on distribution rather than manufacturing, with products such as electrical components and stamped and molded parts. Local sites support operations in nearby locations, and the position involves regular interaction with branch operations and quality teams. Most of the workday is spent on the floor and in the lab, resolving issues and supporting supplier and customer needs, with additional time allocated to supplier visits and audits. Domestic travel typically ranges from about 10% to 20% depending on active projects. The environment supports hands-on problem solving, collaboration with cross-functional teams, and exposure to a wide range of industries and customer applications.Job Type &amp; LocationThis is a Contract to Hire position based out of Solon, OH.Pay and BenefitsThe pay range for this position is $43.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Solon,OH.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Engineer (Contract)Job DescriptionThis short-term Quality Engineer contract role (approximately six months) focuses on providing critical Quality Assurance support by clearing a backlog of investigations and contributing to key QA activities in a regulated environment. You will lead and support investigations related to nonconformances, CAPAs, and complaints, while also assisting with document control, batch release, and document reviews to ensure a full and varied workload throughout the contract. The position requires strong experience in medical devices or similarly regulated industries, excellent root cause analysis capabilities, and clear, precise technical writing skills.Responsibilities<ul><li>Lead and support investigations for nonconformances (NC), CAPAs, and complaints to address a backlog of quality issues in a timely and compliant manner.</li><li>Perform thorough root cause analysis using structured problem-solving methods to identify underlying causes of quality issues and recommend effective corrective and preventive actions.</li><li>Document investigations clearly and accurately, producing high-quality technical reports that meet regulatory and internal quality standards.</li><li>Support additional Quality Assurance activities such as document control, ensuring controlled documents are current, accurate, and properly maintained within the QMS.</li><li>Participate in batch release activities by reviewing relevant documentation for completeness, accuracy, and compliance with applicable standards and procedures.</li><li>Conduct detailed document reviews of procedures, technical documentation, and records to verify compliance with internal quality requirements and regulatory expectations.</li><li>Collaborate closely with the Quality Assurance team and cross-functional partners, including R&amp;D, service, and operations, to gather information and ensure alignment on investigation findings and actions.</li><li>Review and interpret quality system procedures, technical documents, and regulatory requirements to support robust and compliant investigation practices.</li><li>Utilize the QMS system (Qdocs) to manage investigations, documentation, and quality records in an organized and traceable manner.</li><li>Contribute to continuous improvement initiatives within the quality system by identifying trends, recommending process improvements, and supporting implementation of enhanced QA practices.</li></ul>Essential Skills<ul><li>At least 5 years of experience working as a Quality Engineer or QA professional, with a strong focus on investigations.</li><li>Proven experience conducting investigations involving nonconformances (NC), CAPAs, and complaints in a regulated environment.</li><li>Strong understanding of general root cause analysis methodologies and their application to quality issues.</li><li>Excellent technical writing skills, with the ability to produce clear, concise, and well-structured investigation reports and quality documentation.</li><li>Experience working within a Quality Management System (QMS), including use of electronic systems such as Qdocs or similar platforms.</li><li>Background in medical devices is preferred, or substantial experience in a regulated industry such as pharmaceuticals, biotechnology, or other FDA-regulated sectors.</li><li>Knowledge of FDA regulations and expectations related to quality systems, investigations, and CAPA processes.</li><li>Familiarity with ISO standards relevant to quality and medical devices (such as ISO-based QMS frameworks).</li><li>Experience with quality control practices and principles in a regulated environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a medical device environment, including understanding of device lifecycle, risk management, and post-market quality activities.</li><li>Exposure to ISO-based quality standards and their application in daily QA activities.</li><li>Comfort working with cross-functional teams including R&amp;D, service, and operations to gather data and implement corrective and preventive actions.</li><li>Ability to quickly learn and adapt to site-specific QMS tools, including Qdocs, and local procedures.</li><li>Strong attention to detail and organizational skills to manage multiple investigations and documentation tasks simultaneously.</li><li>Effective communication skills, both written and verbal, to present findings and collaborate with stakeholders at different levels.</li><li>Demonstrated ability to work independently while also contributing as a proactive member of a small quality team.</li></ul>Work EnvironmentYou will work as part of a small, collaborative quality team of approximately three other professionals in a hybrid work setting. During the initial phase of the contract, you will spend the majority of your time onsite to receive hands-on training, become familiar with the quality system, and integrate with cross-functional partners. After this training period, a hybrid arrangement with approximately two days in the office each week may be suitable, depending on project needs and performance. The environment is structured and regulated, with a strong emphasis on compliance, documentation accuracy, and adherence to FDA and ISO-based quality standards. You will use a Quality Management System (Qdocs) and other standard office and quality tools to manage investigations, documentation, and batch release activities, working closely with R&amp;D, service, operations, and other stakeholders to support a robust and efficient quality system.Job Type &amp; LocationThis is a Contract position based out of Golden, CO.Pay and BenefitsThe pay range for this position is $40.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Golden,CO.Application DeadlineThis position is anticipated to close on Jul 29, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThis Quality Engineer role focuses on leading customer-facing quality activities, driving problem resolution, and supporting new product launches in an automotive manufacturing environment. You will serve as the primary contact for customers on quality issues, manage quality systems and documentation in line with IATF and automotive standards, and lead continuous improvement initiatives using structured problem-solving tools and lean manufacturing principles. The position offers significant room for growth, including the opportunity to develop into a Quality Manager role, while working with highly automated processes producing interior automotive components such as carpet and felt.Responsibilities<ul><li>Serve as the main point of contact for customers on quality issues and ensure timely, professional communication and resolution.</li><li>Lead corrective action activities (CARs) and drive rapid resolution of quality problems, ensuring sustainable corrective and preventive actions.</li><li>Manage customer complaints, product returns, and non-conforming products from initial identification through closure and documentation.</li><li>Lead Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP) activities for new product launches.</li><li>Ensure all PPAP documentation is accurately prepared, maintained, and submitted on time in accordance with customer and automotive requirements.</li><li>Coordinate Run@Rate activities and launch readiness reviews to verify production capability and readiness for volume manufacturing.</li><li>Maintain compliance with IATF requirements and support the ongoing effectiveness of the quality management system.</li><li>Oversee Statistical Process Control (SPC), process capability studies, Measurement Systems Analysis (MSA), calibration systems, and inspection standards to ensure robust process control.</li><li>Own and maintain key quality documents including PFMEAs, Control Plans, Process Flows, Standard Work, and Work Instructions, ensuring they are current and effective.</li><li>Lead root cause investigations using tools such as 5 Why, Fishbone diagrams, Six Sigma methodologies, and Value Stream Mapping to identify and eliminate sources of defects.</li><li>Implement corrective and preventive actions that improve product quality, reduce defects, and enhance process capability.</li><li>Manage quality requirements for new product launches from prototype through full production, ensuring compliance with customer and internal specifications.</li><li>Coordinate dimensional validation, pre-launch inspections, PPAP sample submission, and other launch-related quality activities.</li><li>Train production teams on new processes, quality requirements, and standards to ensure consistent execution and understanding on the shop floor.</li><li>Lead and support the Quality team by promoting a culture of safety, 5S, professionalism, and continuous improvement.</li><li>Collaborate closely with Engineering, Manufacturing, Maintenance, Suppliers, and other cross-functional teams to address quality concerns and improve processes.</li><li>Provide regular updates to management on launch risks, quality concerns, key metrics, and progress on improvement actions.</li><li>Support supplier quality activities, including communication of requirements, issue resolution, and continuous improvement with suppliers.</li><li>Use data analysis to monitor quality performance, identify trends, and prioritize improvement initiatives.</li><li>Demonstrate leadership without formal authority by influencing cross-functional teams and driving alignment on quality priorities.</li></ul>Essential Skills<ul><li>Bachelor's degree in engineering.</li><li>Minimum of three years of experience working with quality systems, procedures, and practices for an automotive supplier in a manufacturing environment.</li><li>Hands-on experience with quality engineering activities, including quality system documentation and quality systems management.</li><li>Thorough understanding of IATF requirements and automotive standards, including APQP procedures and requirements.</li><li>Proven problem-solving ability, with demonstrated experience using structured root cause analysis tools.</li><li>Launch experience supporting new product introductions in an automotive manufacturing environment.</li><li>Customer interface experience, including managing customer complaints, PPAP submissions, and quality escalations.</li><li>Strong manufacturing process knowledge, particularly in an automotive production setting.</li><li>Data analysis skills, including the ability to interpret SPC, capability studies, and other quality metrics.</li><li>Experience with lean manufacturing principles and practices.</li><li>Ability to provide leadership without formal authority, influencing cross-functional teams toward quality objectives.</li><li>Knowledge of ISO-based quality management systems and ISO standards.</li><li>Strong communication skills, both written and verbal, for effective interaction with customers, internal teams, and suppliers.</li><li>Experience in the automotive industry, preferably with exposure to interior automotive components.</li><li>Familiarity with SAP or similar enterprise systems for managing quality-related data and processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Black Belt certification or equivalent Six Sigma training is highly desirable.</li><li>Experience with ISO-based quality systems and audits.</li><li>Experience in automotive interior manufacturing, such as headliners, door liners, soundproofing materials, carpet, or felt components.</li><li>Supplier quality experience, including working directly with suppliers on quality issues and improvement initiatives.</li><li>Self-starter mindset with the ability to work independently and proactively identify and address quality risks.</li><li>Experience working with highly automated manufacturing processes.</li><li>Interest in and potential for growth into a Quality Manager position.</li><li>Experience supporting or collaborating with another Quality Engineer within a lean quality team structure.</li></ul>Work EnvironmentThis role is based in a manufacturing environment that produces interior automotive components, including carpet and felt for vehicle interiors, as well as related products such as headliners, door liners, and soundproofing materials. The facility features a high level of automation and offers significant opportunities to work with advanced manufacturing technologies and equipment. You will collaborate closely with Engineering, Manufacturing, Maintenance, and Supplier teams on the production floor and in office settings, supporting both day-to-day operations and new product launches. The quality team is lean, with one other Quality Engineer on the team, providing broad exposure and responsibility across quality systems, customer interactions, and continuous improvement initiatives. The organization has previously undergone workforce reductions, so adaptability and a hands-on approach are important. A culture of safety, 5S, professionalism, and continuous improvement is emphasized throughout the work environment.Job Type &amp; LocationThis is a Contract to Hire position based out of Jeffersonville, IN.Pay and BenefitsThe pay range for this position is $43.27 - $45.67/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Jeffersonville,IN.Application DeadlineThis position is anticipated to close on Jul 27, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Engineer Job DescriptionThe Quality Engineer supports the mission of delivering high‑performance medical wire and components by driving quality excellence across CAPA processes, GD&amp;T inspection, and vendor product quality assurance. This role works closely with cross‑functional teams to ensure compliance with regulatory standards and customer expectations, while maintaining robust quality systems and documentation.Responsibilities<ul><li>Lead and support investigations for non-conformances and customer issues, performing thorough root cause analysis using tools such as 5 Whys, fishbone diagrams, and FMEA.</li><li>Develop and implement effective Corrective and Preventive Action (CAPA) plans that address identified root causes and prevent recurrence.</li><li>Monitor CAPA effectiveness, track progress, and ensure timely closure of all actions.</li><li>Maintain complete and accurate CAPA documentation in accordance with ISO standards, FDA Quality System Regulations (QSR), and internal quality system requirements.</li><li>Interpret engineering drawings and specifications that include Geometric Dimensioning and Tolerancing (GD&amp;T) annotations.</li><li>Perform detailed dimensional inspections using coordinate measuring machines (CMM), calipers, micrometers, and other precision metrology tools.</li><li>Document inspection results clearly and ensure full traceability of measurements and inspection records.</li><li>Collaborate with design and manufacturing teams to resolve GD&amp;T-related issues and ensure that product designs meet functional and quality requirements.</li><li>Support validation and verification activities for new and modified products, ensuring that quality and regulatory requirements are met.</li><li>Conduct incoming inspections and quality audits of vendor-supplied products to verify conformance to specifications and standards.</li><li>Review and approve supplier quality documentation, including Production Part Approval Process (PPAP) submissions, First Article Inspections (FAI), and Certificates of Analysis (COA).</li><li>Communicate quality issues to vendors in a clear and timely manner and support them in developing and implementing effective corrective actions.</li><li>Monitor supplier performance metrics and initiate supplier improvement plans when necessary.</li><li>Ensure that all products and supplier processes comply with applicable regulatory, customer, and internal company-specific quality standards.</li><li>Contribute to continuous improvement initiatives within the quality function by leveraging quality engineering tools and best practices.</li></ul>Essential Skills<ul><li>5+ years of experience as a Quality Engineer with a STEM degree, or 10+ years of substantive Quality Engineering experience without a degree (degree preferred).</li><li>Proven experience with quality documentation and CAPA support, including root cause analysis, corrective action planning, and quality system compliance.</li><li>Hands-on experience with Geometric Dimensioning and Tolerancing (GD&amp;T) testing and documentation.</li><li>Ability to interpret engineering drawings and specifications that use GD&amp;T.</li><li>Experience collaborating with design and manufacturing teams to resolve GD&amp;T-related and quality-related issues.</li><li>Demonstrated experience reviewing and auditing PPAP submissions and related supplier quality documentation.</li><li>Experience in supplier quality, including quality inspection and vendor product quality assurance.</li><li>Proficiency in root cause analysis methodologies, including 5 Whys, fishbone diagrams, and FMEA.</li><li>Strong background in quality engineering within a regulated environment, with familiarity with ISO standards and FDA QSR requirements.</li><li>Ability to perform dimensional inspections using CMMs, calipers, micrometers, and other precision metrology tools.</li><li>Strong documentation skills, with the ability to maintain accurate, traceable, and compliant quality records.</li></ul>Additional Skills &amp; Qualifications<ul><li>STEM degree is preferred for candidates with 5+ years of Quality Engineering experience.</li><li>ASQ certification is a nice-to-have and demonstrates a commitment to professional quality standards.</li><li>Experience with Production Part Approval Process (PPAP), First Article Inspection (FAI), and Certificates of Analysis (COA) review.</li><li>Familiarity with supplier performance monitoring and supplier improvement initiatives.</li><li>Comfort working within structured quality systems aligned with ISO and FDA QSR requirements.</li></ul>Work EnvironmentThe role operates in a regulated manufacturing and quality environment focused on high-performance medical wire and components. The Quality Engineer works closely with design, manufacturing, and supplier teams and regularly uses precision metrology equipment such as CMMs, calipers, and micrometers to perform inspections. The position involves extensive interaction with formal quality systems and documentation aligned with ISO standards and FDA Quality System Regulations, as well as routine review of supplier documentation such as PPAP, FAI, and COA. The work environment emphasizes compliance, accuracy, and collaboration across cross-functional teams to ensure consistent product quality and adherence to regulatory and customer requirements.Job Type &amp; LocationThis is a Contract to Hire position based out of Fort Wayne, IN.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Fort Wayne,IN.Application DeadlineThis position is anticipated to close on Jul 28, 2026.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

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