Description
					Perform quality inspections on raw materials, in-process products, and finished goods to ensure compliance with food safety and quality standards.
Monitor and document product weights, temperatures, and case specifications throughout the manufacturing process.
Verify packaging accuracy, including product codes, date codes, and labeling requirements.
Collect, test, and document product samples for laboratory analysis and quality evaluations.
Identify, document, and hold non-conforming products for further investigation and corrective action.
Monitor production processes and metal detection systems to ensure product safety and regulatory compliance.
Ensure adherence to Good Manufacturing Practices (GMPs), HACCP requirements, and company quality standards.
Support a safe, sanitary, and compliant production environment through routine inspections and monitoring.
Investigate, document, and communicate quality concerns to support continuous improvement efforts.
Complete special projects and additional quality assurance duties as assigned.
					 					Skills
					Quality assurance, food safety, Haccp, Fda, usda, Gmp, Quality control, Inspection, Sop, sample testing, Document control, Food manufacturing, Laboratory, Food quality, Batch record review
					 					Top Skills Details
					Quality assurance,food safety,Haccp,Fda,usda,Gmp,Quality control,Inspection,Sop,sample testing
					 					Additional Skills &amp; Qualifications
					•	Required High School diploma, GED or equivalent, with basic math and computer skills to work with Mi-crosoft Word, Excel, PowerPoint, and are comfortable with electronic data collection
•	Must be dependable, available during required work hours, and be willing to work weekends and overtime hours as company necessitates.
•	Detail-oriented with abilities to follow directions, to record data neatly and accurately, to work under minimal supervision, to multi-task in fast paced environment safety, and to communicate effectively and clearly in a timely manner, both verbally and in writing.
•	Desired experience with Food Manufacturing, Food Service, and Retail Operations
					 					Experience Level
					Entry Level
					 Job Type &amp; LocationThis is a Contract to Hire position based out of Davenport, IA.Pay and BenefitsThe pay range for this position is $19.00 - $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 Davenport,IA.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.

public

QA Technician

QA TechnicianDescription<ul><li>Perform quality inspections on raw materials, in-process products, and finished goods to ensure compliance with food safety and quality standards.</li><li>Monitor and document product weights, temperatures, and case specifications throughout the manufacturing process.</li><li>Verify packaging accuracy, including product codes, date codes, and labeling requirements.</li><li>Collect, test, and document product samples for laboratory analysis and quality evaluations.</li><li>Identify, document, and hold non-conforming products for further investigation and corrective action.</li><li>Monitor production processes and metal detection systems to ensure product safety and regulatory compliance.</li><li>Ensure adherence to Good Manufacturing Practices (GMPs), HACCP requirements, and company quality standards.</li><li>Support a safe, sanitary, and compliant production environment through routine inspections and monitoring.</li><li>Investigate, document, and communicate quality concerns to support continuous improvement efforts.</li><li>Complete special projects and additional quality assurance duties as assigned.</li></ul> Qualifications<ul><li>Required High School diploma, GED or equivalent, with basic math and computer skills to work with Mi-crosoft Word, Excel, PowerPoint, and are comfortable with electronic data collection</li><li>Must be dependable, available during required work hours, and be willing to work weekends and overtime hours as company necessitates.</li><li>Detail-oriented with abilities to follow directions, to record data neatly and accurately, to work under minimal supervision, to multi-task in fast paced environment safety, and to communicate effectively and clearly in a timely manner, both verbally and in writing.</li><li>Desired experience with Food Manufacturing, Food Service, and Retail Operations</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Davenport, Iowa.Pay and BenefitsThe pay range for this position is $19.00 - $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 Davenport,Iowa.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 Assurance TechnicianJob DescriptionThe Quality Assurance Technician inspects finished products, verifies processing activities, and evaluates both finished goods and work in progress to support continuous improvement in quality and efficiency. This role conducts routine quality checks, maintains detailed records, and helps ensure that all products meet established specifications, food safety requirements, and customer expectations.Comes with a $4 shift differential increase, offering pay up to $28/hour (or more based on experience)Responsibilities<ul><li>Perform inspections of finished products and work in progress to confirm they meet quality specifications and customer requirements.</li><li>Complete and review all required quality assurance paperwork and electronic records accurately and on time.</li><li>Conduct routine floor audits of production and packaging areas to verify correct product composition, specifications, storage, packaging, labeling, and coding.</li><li>Assist with completion of compliance checks for production runs at scheduled frequencies, including weights, case checks, label verifications, case verifications, product coding requirements, and customer-driven testing.</li><li>Monitor facility activities with daily inspections and document findings in accordance with quality and food safety programs.</li><li>Inspect, review, and complete pre-operational swabbing and quality program records on a daily basis.</li><li>Report quality-related failures or potential food safety issues to quality and department leadership and document follow-up actions.</li><li>Assist the quality assurance leadership team with execution of sales and customer sample request programs.</li><li>Initiate hold procedures for products manufactured out of specification and communicate product status and disposition to affected departments.</li><li>Initiate defective material reports for vendor-supplied products that do not meet specifications or cannot be used.</li><li>Maintain and inspect retain samples to identify and investigate potential product quality issues.</li><li>Execute environmental monitoring, product testing, chemical testing, and glass inspections throughout the facility.</li><li>Complete accurate data entry for laboratory and production results in the appropriate systems.</li><li>Support continuous improvement of day-to-day operations to maximize product quality and operational efficiency.</li><li>Perform additional duties and responsibilities as assigned by leadership to support the overall quality program.</li></ul>Essential Skills<ul><li>High school diploma or equivalent.</li><li>Basic understanding of quality assurance principles and practices.</li><li>Physical ability to stand for most of the shift and lift more than 20 pounds.</li><li>Comfort working on an overnight shift schedule.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate’s degree in Food Science, Biology, Chemistry, or a related field preferred.</li><li>Prior food manufacturing quality assurance experience is a strong plus.</li><li>Experience in food manufacturing, food safety, or food production environments.</li><li>Familiarity with ERP systems such as Deacom, RedZone, or similar platforms.</li></ul>Work EnvironmentThis role is based on a manufacturing floor environment, with frequent movement between mixing and blending rooms and the production floor. The position requires spending the majority of the shift on your feet, with moderate noise levels typical of a production facility. The shift runs from 10:00 p.m. to 6:30 a.m., Monday night through Saturday morning, and includes a shift differential for third shift. Overtime may be available based on business needs, which can include a rotating weekend schedule, most likely on Saturdays. The facility operates in a bilingual environment with both Spanish- and English-speaking team members. The work involves handling quality testing equipment, performing environmental and product testing, and lifting items over 20 pounds as needed.Job Type &amp; LocationThis is a Contract to Hire position based out of Hopkins, MN.Pay and BenefitsThe pay range for this position is $20.00 - $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 Hopkins,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.

QA Technician - $24-28/hour - Overnights And Days

Job Title: QAPC Lab TechnicianJob DescriptionWe are seeking a qualified Lab Technician to perform a variety of technical laboratory procedures. This role involves handling chemicals and using sensitive equipment to analyze samples, conduct tests, and report findings that aid in operational decisions. The technician will work closely with the Process Control Lab (QAPC) team leader. The position requires a commitment to maintaining safe work conditions and a passion for contributing to the production of quality finished goods.Responsibilities<ul><li>Receive and analyze samples from production, innovation teams, and special projects.</li><li>Safely execute laboratory testing according to standard procedures, make observations and interpret findings.</li><li>Organize and store all chemical substances, fluids, and compressed gases according to safety instructions.</li><li>Accurately document all data and results in specified forms, both paper and electronic.</li><li>Maintain laboratory equipment and assist in ordering supplies.</li><li>Ensure strict adherence to all safety guidelines and maintain a clean, orderly environment.</li></ul>Essential Skills<ul><li>Proven experience as a Lab Technician or relevant position.</li><li>Experience in operating electrical and non-electrical laboratory equipment and handling potentially dangerous substances such as flammable liquids, acids, and bases.</li><li>Knowledge of SHE systems, preventative measures, and laboratory best practices.</li><li>Working knowledge of MS Office suite (especially Excel), database systems, and Teams.</li><li>Ability to work autonomously and under pressure.</li><li>Degree in biology, chemistry, or a relevant field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with quality control processes.</li><li>Experience in laboratory best practices.</li></ul>Work EnvironmentThe work environment is a manufacturing paint lab, where the technician will initially train for 30–60 days with a schedule from Monday to Thursday, 7:00 AM – 5:00 PM. After training, the technician will transition to a night shift schedule with a 2-2-3 rotation, working from 7:00 PM – 7:00 AM. The company offers retention bonuses at 3, 6, 12, and 18 months.Job Type &amp; LocationThis is a Contract position based out of Goose Creek, SC.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 Goose Creek,SC.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.

QAPC Lab Technician

Job Title: QAPC Lab Technician Job DescriptionWe are seeking a qualified Lab Technician to perform a variety of technical laboratory procedures. This role involves handling chemicals and using sensitive equipment to analyze samples, conduct tests, and report findings that aid in operational decisions. The technician will work closely with the Process Control Lab (QAPC) team leader. The position requires a commitment to maintaining safe work conditions and a passion for contributing to the production of quality finished goods.Responsibilities<ul><li>Receive and analyze samples from production, innovation teams, and special projects.</li><li>Safely execute laboratory testing according to standard procedures, make observations and interpret findings.</li><li>Organize and store all chemical substances, fluids, and compressed gases according to safety instructions.</li><li>Accurately document all data and results in specified forms, both paper and electronic.</li><li>Maintain laboratory equipment and assist in ordering supplies.</li><li>Ensure strict adherence to all safety guidelines and maintain a clean, orderly environment.</li></ul>Essential Skills<ul><li>Proven experience as a Lab Technician or relevant position.</li><li>Experience in operating electrical and non-electrical laboratory equipment and handling potentially dangerous substances such as flammable liquids, acids, and bases.</li><li>Knowledge of SHE systems, preventative measures, and laboratory best practices.</li><li>Working knowledge of MS Office suite (especially Excel), database systems, and Teams.</li><li>Ability to work autonomously and under pressure.</li><li>Degree in biology, chemistry, or a relevant field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with quality control processes.</li><li>Background in laboratory best practices.</li></ul>Work EnvironmentThe work environment is a manufacturing paint lab, where the technician will initially train for 30–60 days with a schedule from Monday to Thursday, 7:00 AM – 5:00 PM. After training, the technician will transition to a night shift schedule with a 2-2-3 rotation, working from 7:00 PM – 7:00 AM. The company offers retention bonuses at 3, 6, 12, and 18 months.Job Type &amp; LocationThis is a Contract position based out of Goose Creek, SC.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 Goose Creek,SC.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 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.

QC Chemist

<h2>QC Chemist</h2><h3>Position Summary</h3>The QC Chemist is responsible for sampling, testing, documenting, and releasing incoming raw materials used in cosmetic and personal care manufacturing. This role ensures materials meet quality, regulatory, and specification requirements prior to production.<h3>Key Responsibilities</h3><ul><li>Sample, inspect, and test incoming raw materials and packaging components.</li><li>Perform analytical and physical testing, including pH, viscosity, specific gravity, appearance, odor, color, moisture, and FTIR analysis.</li><li>Evaluate results and determine material disposition (release, reject, or quarantine).</li><li>Conduct wet chemistry testing and operate laboratory equipment, including pH meters, titrators, balances, and spectrophotometers.</li><li>Maintain accurate laboratory documentation in compliance with cGMP, GLP, SOPs, and data integrity requirements.</li><li>Perform instrument calibration, verification, and routine maintenance.</li><li>Assist with OOS investigations, corrective actions, and vendor qualification activities.</li><li>Maintain laboratory inventory and ensure the lab remains organized and audit-ready.</li><li>Collaborate with Quality, Manufacturing, Warehouse, and Supply Chain teams.</li><li>Support continuous improvement initiatives and perform other duties as assigned.</li></ul><h3>Qualifications</h3>Education<ul><li>Bachelor's degree in Chemistry, Biochemistry, Biology, or related scientific field preferred.</li><li>Associate degree with relevant laboratory experience may be considered.</li></ul>Experience<ul><li>1-2 years of Quality Control laboratory experience preferred.</li><li>Cosmetics, personal care, pharmaceutical, food, or other regulated manufacturing experience is a plus.</li><li>Experience with raw material testing and release activities preferred.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Chatsworth, CA.Pay and BenefitsThe pay range for this position is $25.00 - $28.00/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 Chatsworth,CA.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.

<h1>QC Chemist </h1><h2>About the Role</h2>We are seeking a detail-oriented QC Chemist to join our Quality Control team in a GMP-regulated laboratory environment. In this role, you will perform analytical testing of raw materials, in-process samples, and finished products to ensure compliance with quality and regulatory standards. This is an excellent opportunity for a chemist with hands-on HPLC experience who enjoys working in a collaborative, science-driven environment and wants to expand their expertise across a variety of analytical techniques and instrumentation.<h2>Key Responsibilities</h2><ul><li>Perform routine and non-routine analytical testing using HPLC and other laboratory instrumentation.</li><li>Analyze raw materials, in-process samples, and finished products according to approved test methods.</li><li>Prepare samples, reagents, standards, and mobile phases for laboratory testing.</li><li>Accurately document analytical results and maintain laboratory records in compliance with GMP, SOPs, and data integrity requirements.</li><li>Calibrate, maintain, and troubleshoot laboratory equipment as needed.</li><li>Participate in laboratory investigations, deviations, and out-of-specification (OOS) activities.</li><li>Collaborate with cross-functional team members to support testing schedules and product release timelines.</li><li>Manage multiple analytical methods and instruments with a high degree of accuracy and attention to detail once fully trained.</li></ul><h2>Required Qualifications</h2><ul><li>Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline.</li><li>Minimum of 2 years of experience in a Quality Control or analytical laboratory environment.</li><li>Hands-on experience operating and troubleshooting HPLC systems.</li><li>Experience preparing samples, interpreting analytical data, and documenting laboratory activities in a regulated setting.</li><li>Knowledge of GMP regulations, SOP compliance, data integrity principles, and quality standards.</li><li>Strong organizational skills with the ability to manage multiple priorities in a fast-paced laboratory environment.</li><li>Excellent attention to detail and commitment to producing high-quality results.</li></ul><h2>Preferred Qualifications</h2>Experience with one or more of the following is highly desirable:<ul><li>UPLC</li><li>Gas Chromatography (GC)</li><li>USP Compendial Testing</li><li>Elemental Analysis</li><li>Mass Spectrometry (MS)</li><li>LC/MS</li><li>FTIR</li><li>Chromatography method execution and troubleshooting</li><li>Pharmaceutical manufacturing or pharmaceutical quality systems</li></ul><h2>Work Environment</h2><ul><li>100% onsite laboratory-based position</li><li>First Shift: Monday through Friday, 8:00 AM to 5:00 PM</li><li>Collaborative team of approximately 8 laboratory professionals</li><li>Structured onboarding, mentorship, and hands-on training program</li><li>Opportunity to work independently once training and competency requirements are completed</li><li>Occasional extended days may be required to support analytical testing and instrument run schedules</li></ul><h2>Why this position?</h2><ul><li>Gain exposure to a broad range of analytical techniques and instrumentation</li><li>Work in a collaborative, team-oriented GMP laboratory</li><li>Receive hands-on mentorship and professional development opportunities</li><li>Contribute directly to product quality and regulatory compliance in a highly regulated industry</li></ul>Job Type &amp; LocationThis is a Contract position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $24.00 - $28.00/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 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.

Job Title: QC ChemistJob DescriptionThe QC Chemist works in a quality control laboratory within a pharmaceutical and specialty chemical manufacturing environment in the Milwaukee area. This role focuses on release and in-process testing of raw materials, intermediates, and finished API products using a wide range of analytical instrumentation. The QC Chemist interprets chromatography data, manages analytical documentation in compliance with GMP requirements, and contributes to method and analytical development in a growing, expansion-focused organization.Responsibilities<ul><li>Perform release and in-process testing of raw materials, intermediates, test materials, and finished API products in accordance with written methods and procedures.</li><li>Follow all applicable procedures, specifications, and test methods, ensuring full compliance with internal and regulatory requirements.</li><li>Execute wet chemistry and analytical chemistry techniques to support quality control activities.</li><li>Operate and utilize laboratory instrumentation, including HPLC, GC, FTIR, UV-Vis, Karl Fischer (KF), IC, and a soon-to-be-installed ICP-MS, to perform routine and specialized analyses.</li><li>Interpret chromatography data and other analytical results, using data management systems such as Chemstation or Chromeleon where applicable.</li><li>Assess whether materials meet specifications for release and document decisions clearly and accurately.</li><li>Perform and review critical and complex calculations to support analytical testing and data evaluation.</li><li>Prepare and standardize volumetric solutions to support routine and non-routine testing.</li><li>Clearly document all GMP activities accurately and legibly, maintaining complete and compliant laboratory records.</li><li>Perform routine maintenance and basic troubleshooting on QC instrumentation to ensure reliable operation.</li><li>Review data calculations for validation activities and ensure accuracy of analytical results.</li><li>Provide information and documentation responses in cases of customer complaints or returns, supporting investigations and resolutions.</li><li>Write procedures, test methods, protocols, reports, and material specifications to support laboratory operations and continuous improvement.</li><li>Support a culture of consistent compliance by participating in training, providing guidance, and reviewing procedures as needed.</li><li>Meet deadlines and testing schedules established by quality control leadership.</li><li>Participate in a structured training process, progressing from observing tests, to performing tests under supervision, to independently executing tests.</li><li>Handle laboratory supplies such as columns, liners, and septa, and ensure proper setup and use of analytical equipment.</li><li>Lift up to 25 pounds as needed to handle materials, reagents, and equipment in the laboratory.</li></ul>Essential Skills<ul><li>Bachelor’s degree in a science discipline such as Chemistry, Biochemistry, or Biology.</li><li>2–3 years of experience as a chemist in an industrial setting.</li><li>Hands-on experience with HPLC and GC in a quality control or analytical laboratory environment.</li><li>Proficiency with laboratory instrumentation, including HPLC, GC, FTIR, UV-Vis, Karl Fischer (KF), and IC.</li><li>Ability to interpret and review analytical and chromatographic data accurately.</li><li>Strong competency in performing and verifying critical and complex calculations.</li><li>Experience working under GMP or similar regulated quality systems, with the ability to document activities clearly and legibly.</li><li>At least 2 years of experience using Excel for data analysis, reporting, and documentation.</li><li>Capability to prepare and standardize volumetric solutions and perform wet chemistry techniques.</li><li>Ability to write clear and concise procedures, test methods, protocols, reports, and material specifications.</li><li>Capacity to perform routine maintenance and basic troubleshooting on QC instrumentation.</li><li>Ability to assess whether materials meet specifications for release based on analytical results.</li><li>Physical ability to lift up to 25 pounds as part of laboratory duties.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with data management systems such as Chemstation or Chromeleon.</li><li>Familiarity with NMR and broader analytical chemistry techniques.</li><li>Experience with API, flavor and fragrance, or specialty chemical environments.</li><li>Comfort working in smaller organizations where chemists gain exposure to a wide range of analytical equipment and responsibilities.</li><li>Interest in contributing to analytical development, method development, and validation activities.</li><li>Strong attention to detail and a commitment to maintaining high-quality standards in all laboratory work.</li><li>Ability to work collaboratively with another chemist and cross-functional teams in both laboratory and manufacturing settings.</li></ul>Work EnvironmentThe QC Chemist works in a quality laboratory that supports API, flavor and fragrance, and specialty chemical manufacturing. The role involves primarily laboratory-based work with occasional visits to the manufacturing floor. The laboratory uses a broad range of analytical technologies, including HPLC, GC, FTIR, UV-Vis, Karl Fischer (KF), IC, and a soon-to-be-installed ICP-MS, providing extensive hands-on experience with modern analytical equipment. The organization is a smaller company, which allows chemists to gain broad exposure to analytical instruments and to participate in analytical and method development, as well as validation activities. The facility is currently expanding, with an additional building being added to increase API manufacturing capabilities and enhance laboratory operations. Work is conducted on a first-shift schedule, with initial training typically running from 8:00 a.m. to 4:30 p.m., followed by a standard shift of 7:00 a.m. to 3:30 p.m. The environment emphasizes GMP compliance, accurate documentation, and collaboration. Annual pay raises are performance-based, with typical increases averaging around 4% of salary per year. Dress is consistent with a professional laboratory and manufacturing setting, including appropriate lab attire and any required personal protective equipment.Job Type &amp; LocationThis is a Permanent position based out of St Francis, WI.Pay and BenefitsThe pay range for this position is $62000.00 - $62000.00/yr.Kingchem Laboratories offers a range of internal employee benefits designed to support both professional growth and personal well-being. Employees typically have access to competitive health insurance options, retirement savings plans, and paid time off to promote work-life balance. The company also emphasizes career development through on-the-job training, mentorship, and opportunities to advance within technical and quality-focused roles. Additionally, Kingchem fosters a collaborative culture with performance incentives, recognition programs, and a strong focus on safety and compliance in the workplace.Workplace TypeThis is a fully onsite position in St Francis,WI.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.

Actalent Scientific is seeking a licensed QC Lab Analyst for full time role in a quality control laboratory within a chemical processing facilityin Jacksonville, FL. Qualified candidates must must meet the following criteria:QUALIFICATIONS:·      Bachelor level degree in chemistry or similar scientific discipline ·      1+ year of industry, quality laboratory experience with Gas Chromatography·      Ability to work in fast paced environment·      Strong communication skills  Job Type &amp; LocationThis is a Contract to Hire position based out of JACKSONVILLE, FL.Pay and BenefitsThe pay range for this position is $20.00 - $22.50/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 JACKSONVILLE,FL.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.

QC Lab Technician

Job Title: QC Laboratory Support Technician Job DescriptionThe QC Laboratory Support Technician (Technician II, QC Laboratory Support) works as part of a team dedicated to supporting Quality Control laboratory operations. This role focuses on managing analytical testing samples and backups, analytical standards, assay controls, laboratory reagents, and overall laboratory inventory. The technician provides ongoing, non-testing support so that laboratory analysts can perform analytical testing more efficiently and effectively. This position does not involve hands-on testing of product samples and instead concentrates on logistical, organizational, and quality-focused support activities within a GMP/GLP environment.Responsibilities<ul><li>Collaborate routinely with laboratory analysts to ensure they have all required supplies, reagents, and materials prior to testing initiation.</li><li>Use a variety of information management systems and tools to manage inventory and logistics for samples, standards, assay controls, critical reagents, consumables, and other items that support QC laboratory operations.</li><li>Support laboratory analysts with non-billable activities such as glassware handling and labeling, laboratory waste management, laboratory inspections and walkthroughs, labeling tasks, and maintenance of kanban and 5S systems.</li><li>Assist with the creation and monitoring of purchase requisitions, purchase orders, and other procurement processes to ensure timely fulfillment of laboratory inventory requirements.</li><li>Collect, wash, and re-distribute laboratory glassware in a consistent and organized manner.</li><li>Manage the transport of laboratory waste to designated Environmental Health and Safety (EHS) drop-off areas in accordance with site procedures.</li><li>Assist with laboratory preventive maintenance (PM) activities where appropriate and as directed.</li><li>Perform additional laboratory support duties, including future non-billable and non-critical tasks, as needed to help the department meet its goals.</li><li>Maintain accurate documentation related to inventory, glassware handling, labeling, and other support activities, with strong attention to detail.</li><li>Apply knowledge of GMP/GLP and cGMP practices to daily work to support quality and compliance in the laboratory environment.</li></ul>Essential Skills<ul><li>Minimum of a high school diploma.</li><li>0–3 years of experience working in a GMP-regulated environment.</li><li>1–3 years of experience in a GLP/GMP laboratory or GMP manufacturing facility in a laboratory or quality role.</li><li>Working knowledge of GMP regulations in a GMP environment.</li><li>Knowledge of cGMP practices and aseptic techniques.</li><li>Experience or familiarity with quality assurance and quality control concepts in a laboratory setting.</li><li>Experience with sample preparation, sample management, and laboratory preparation activities.</li><li>Strong attention to detail, especially in cleaning and handling glassware and in completing documentation accurately.</li><li>Comfort using computers and working with different systems, software tools, and Excel.</li><li>Ability to support laboratory operations through non-testing tasks such as inventory management, labeling, and waste handling.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate’s degree, preferably in a STEM discipline.</li><li>Working experience in a cGMP Quality Control laboratory.</li><li>Working experience with sample labeling systems.</li><li>Working experience with inventory management systems.</li><li>Pharmacy technician experience, particularly in a regulated environment.</li><li>Familiarity with kanban and 5S systems for organizing laboratory workflows.</li><li>Demonstrated ability to support quality-focused environments such as GMP/GLP laboratories or manufacturing facilities.</li><li>Interest in a contract-to-hire opportunity contingent on strong performance.</li></ul>Work EnvironmentThe position is based in a Quality Control laboratory environment that operates under GMP, GLP, and cGMP standards. The role follows a Monday through Friday schedule, typically from 8:00 a.m. to 4:30 p.m. The technician works closely with laboratory analysts and other quality professionals, using computers and various software systems, including inventory management tools, sample labeling systems, and Excel. The work involves frequent handling of glassware, laboratory reagents, and consumables, as well as routine movement of laboratory waste to designated EHS drop-off areas. The environment emphasizes organization, cleanliness, and adherence to 5S and kanban principles to support efficient laboratory operations. The culture supports growth through a contract-to-hire structure, providing the opportunity to transition to a longer-term role based on performance.Job Type &amp; LocationThis is a Contract to Hire position based out of St. Louis, MO.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 St. 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.

QC Laboratory Support Technician

Job Title: Specialist, Quality Control – Microbiologist (Contract) Job DescriptionThis contract Quality Control Microbiologist role plays a critical part in supporting high-precision cell therapy manufacturing by overseeing key quality systems and ensuring that products meet rigorous regulatory and internal standards before release. Based on-site in Sacramento, CA, the specialist manages deviations, change controls, CAPAs, and document control, while contributing to batch disposition decisions that directly impact patients receiving next‑generation cell therapies. The position offers approximately six months of maternity leave coverage, working in a fast‑paced, highly regulated environment where scientific excellence, data integrity, and collaboration are central to the mission.Responsibilities<ul><li>Oversee the management of quality systems, including deviations, change controls, CAPAs, and document control, ensuring they operate effectively and in compliance with internal procedures.</li><li>Investigate deviations thoroughly and in a timely manner, identify root causes, and implement effective corrective and preventive actions.</li><li>Review and approve change controls to ensure alignment with regulatory requirements and established quality standards.</li><li>Maintain and continuously improve CAPA processes to drive effective resolution of quality issues and prevent recurrence.</li><li>Evaluate batch records and associated documentation to make informed batch release decisions in support of rapid processing timelines.</li><li>Collaborate closely with manufacturing and quality control teams to ensure all products meet regulatory and quality standards prior to release.</li><li>Monitor, document, and address any quality issues related to batch production, implementing corrective measures as needed.</li><li>Maintain the document management system so that all quality-related documents are accurate, current, and compliant with regulatory expectations.</li><li>Conduct regular reviews of quality documentation to confirm adherence to established protocols and procedures.</li><li>Stay current on applicable FDA regulations, GMP requirements, and industry best practices in pharmaceutical and cell therapy quality assurance.</li><li>Assist in preparation for internal and external audits, ensuring that quality systems and documentation remain audit‑ready.</li><li>Provide training and guidance to staff on quality systems, processes, and compliance requirements, supporting a strong culture of quality.</li><li>Serve as a point of contact for quality-related inquiries and issues, offering clear direction and support to cross‑functional partners.</li><li>Participate in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes.</li><li>Identify areas for improvement within quality operations, propose appropriate solutions, and help implement agreed‑upon changes.</li><li>Track completion of quality records, maintain metrics, and report on key quality performance indicators as required.</li><li>Perform internal audits and support document control management activities to strengthen compliance and data integrity.</li><li>Carry out additional duties as requested to support overall Quality objectives and regulatory compliance.</li><li>Work collaboratively with cross-functional teams, including manufacturing, research and development, and quality assurance, to support the overall quality of cell therapy products.</li><li>Communicate effectively with team members and contribute to a positive, collaborative work environment.</li><li>Actively participate in group and project teamwork, including project and process improvement initiatives.</li><li>Adhere to cGMP policies and procedures, including meticulous documentation practices and proper use of personal protective equipment.</li><li>Meet project and testing timelines while managing multiple tasks concurrently in a dynamic setting.</li><li>Provide on‑call support outside regular business hours as needed and work overtime when required to meet business needs.</li></ul>Essential Skills<ul><li>Bachelor’s degree in a relevant scientific discipline such as biology, biochemistry, immunology, or a related field with 3+ years of experience in quality control testing, analytical development, or GMP; or a Master’s degree in a relevant scientific discipline with 1+ years of experience.</li><li>Hands-on experience in quality control or GMP operations, preferably within a cell therapy or biopharmaceutical manufacturing environment.</li><li>Strong understanding of FDA regulations, GMP compliance requirements, and quality system processes.</li><li>Demonstrated experience managing deviations, change controls, CAPAs, and document control within a regulated environment.</li><li>Experience running validation activities and handling CAPAs, including authoring or reviewing validation reports.</li><li>Knowledge of environmental monitoring and quality control methodologies in a pharmaceutical or biotechnology setting.</li><li>Proven ability to meet project and testing timelines while maintaining high standards of quality and compliance.</li><li>High level of attention to detail with a strong commitment to data integrity and accuracy, including the ability to identify and resolve data management issues.</li><li>Ability to work both independently and collaboratively within a multi‑disciplinary team in a fast‑paced, highly regulated environment.</li><li>Strong organizational skills with the ability to manage multiple tasks concurrently and adapt to changing priorities and challenges.</li><li>Effective verbal and written communication skills, with the ability to convey complex quality concepts clearly to diverse stakeholders.</li><li>Ability to adhere to cGMP policies and procedures and to wear appropriate personal protective equipment in production and cleanroom areas.</li><li>Willingness and ability to work scheduled overtime, weekends, or holidays as required by business needs, and to provide on‑call support outside regular business hours.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior experience performing internal audits and supporting document control management in a GMP or FDA‑regulated environment.</li><li>Experience with validation planning, execution, and reporting for quality control systems or equipment.</li><li>Background in environmental monitoring programs and related quality oversight within manufacturing or laboratory settings.</li><li>Familiarity with CAPA management tools and electronic quality management systems.</li><li>Exposure to cell therapy or advanced biologics manufacturing processes and associated quality control testing.</li><li>Ability to contribute to continuous improvement initiatives, including process optimization and system enhancements.</li><li>Comfort working in a fast‑paced, entrepreneurial environment with evolving processes and responsibilities.</li><li>Demonstrated willingness to learn new technologies and approaches in support of innovative cell therapy development.</li><li>Approximately six‑month availability to provide maternity leave coverage in a contract or consultant capacity.</li></ul>Work EnvironmentThis role is based on-site at dedicated clinical manufacturing facilities in Sacramento, CA, supporting production of high‑precision cell therapy products in a GMP‑regulated environment. The specialist works closely with manufacturing, quality control, research and development, and quality assurance teams in a fast‑paced, dynamic setting that emphasizes scientific rigor, data integrity, and patient impact. Work may involve regular participation in video‑based meetings and collaboration with colleagues across multiple locations. The environment includes cleanroom operations where strict gowning requirements apply, including wearing full gowning such as face coverings, gloves, hoods, and goggles for extended periods when needed. Use of cosmetics, painted nails, jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed to ensure safety and product quality. Team members must be able to meet visual acuity requirements and normal color vision standards to perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color‑coded components. Work hours follow standard business schedules but may require overtime, weekend, or holiday work based on operational needs, as well as occasional on‑call support outside regular business hours. The broader organization maintains a start‑up culture characterized by camaraderie, leadership by example, and an entrepreneurial spirit that encourages innovation, calculated risk‑taking, and challenging the status quo. Employees are supported with comprehensive benefits, including medical, dental, and vision coverage, PTO, retirement plan options, life and disability coverage, parental leave, and on‑site perks such as subsidized daily lunches and snacks. The culture is driven by passion for science, compassion for patients, and core values of passion, courage, and integrity, with a strong commitment to equal opportunity and inclusive collaboration.Job Type &amp; LocationThis is a Contract position based out of Sacramento, CA.Pay and BenefitsThe pay range for this position is $40.00 - $50.00/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 Sacramento,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.

QC Microbiologist

Job Title: Specialist, Quality Control – Microbiologist, must have validation experience and writing the reports.M-F DAY shift 7 am to 3:30 pm.First couple of weeks onsite, then remote.Job DescriptionThis contract Quality Control Microbiologist role plays a critical part in supporting high-precision cell therapy manufacturing by overseeing key quality systems and ensuring that products meet rigorous regulatory and internal standards before release. Based on-site in Sacramento, CA, the specialist manages deviations, change controls, CAPAs, and document control, while contributing to batch disposition decisions that directly impact patients receiving next‑generation cell therapies. The position offers approximately six months of maternity leave coverage, working in a fast‑paced, highly regulated environment where scientific excellence, data integrity, and collaboration are central to the mission.Responsibilities<ul><li>Oversee the management of quality systems, including deviations, change controls, CAPAs, and document control, ensuring they operate effectively and in compliance with internal procedures.</li><li>Investigate deviations thoroughly and in a timely manner, identify root causes, and implement effective corrective and preventive actions.</li><li>Review and approve change controls to ensure alignment with regulatory requirements and established quality standards.</li><li>Maintain and continuously improve CAPA processes to drive effective resolution of quality issues and prevent recurrence.</li><li>Evaluate batch records and associated documentation to make informed batch release decisions in support of rapid processing timelines.</li><li>Collaborate closely with manufacturing and quality control teams to ensure all products meet regulatory and quality standards prior to release.</li><li>Monitor, document, and address any quality issues related to batch production, implementing corrective measures as needed.</li><li>Maintain the document management system so that all quality-related documents are accurate, current, and compliant with regulatory expectations.</li><li>Conduct regular reviews of quality documentation to confirm adherence to established protocols and procedures.</li><li>Stay current on applicable FDA regulations, GMP requirements, and industry best practices in pharmaceutical and cell therapy quality assurance.</li><li>Assist in preparation for internal and external audits, ensuring that quality systems and documentation remain audit‑ready.</li><li>Provide training and guidance to staff on quality systems, processes, and compliance requirements, supporting a strong culture of quality.</li><li>Serve as a point of contact for quality-related inquiries and issues, offering clear direction and support to cross‑functional partners.</li><li>Participate in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes.</li><li>Identify areas for improvement within quality operations, propose appropriate solutions, and help implement agreed‑upon changes.</li><li>Track completion of quality records, maintain metrics, and report on key quality performance indicators as required.</li><li>Perform internal audits and support document control management activities to strengthen compliance and data integrity.</li><li>Carry out additional duties as requested to support overall Quality objectives and regulatory compliance.</li><li>Work collaboratively with cross-functional teams, including manufacturing, research and development, and quality assurance, to support the overall quality of cell therapy products.</li><li>Communicate effectively with team members and contribute to a positive, collaborative work environment.</li><li>Actively participate in group and project teamwork, including project and process improvement initiatives.</li><li>Adhere to cGMP policies and procedures, including meticulous documentation practices and proper use of personal protective equipment.</li><li>Meet project and testing timelines while managing multiple tasks concurrently in a dynamic setting.</li><li>Provide on‑call support outside regular business hours as needed and work overtime when required to meet business needs.</li></ul>Essential Skills<ul><li>Bachelor’s degree in a relevant scientific discipline such as biology, biochemistry, immunology, or a related field with 3+ years of experience in quality control testing, analytical development, or GMP; or a Master’s degree in a relevant scientific discipline with 1+ years of experience.</li><li>Hands-on experience in quality control or GMP operations, preferably within a cell therapy or biopharmaceutical manufacturing environment.</li><li>Strong understanding of FDA regulations, GMP compliance requirements, and quality system processes.</li><li>Demonstrated experience managing deviations, change controls, CAPAs, and document control within a regulated environment.</li><li>Experience running validation activities and handling CAPAs, including authoring or reviewing validation reports.</li><li>Knowledge of environmental monitoring and quality control methodologies in a pharmaceutical or biotechnology setting.</li><li>Proven ability to meet project and testing timelines while maintaining high standards of quality and compliance.</li><li>High level of attention to detail with a strong commitment to data integrity and accuracy, including the ability to identify and resolve data management issues.</li><li>Ability to work both independently and collaboratively within a multi‑disciplinary team in a fast‑paced, highly regulated environment.</li><li>Strong organizational skills with the ability to manage multiple tasks concurrently and adapt to changing priorities and challenges.</li><li>Effective verbal and written communication skills, with the ability to convey complex quality concepts clearly to diverse stakeholders.</li><li>Ability to adhere to cGMP policies and procedures and to wear appropriate personal protective equipment in production and cleanroom areas.</li><li>Willingness and ability to work scheduled overtime, weekends, or holidays as required by business needs, and to provide on‑call support outside regular business hours.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior experience performing internal audits and supporting document control management in a GMP or FDA‑regulated environment.</li><li>Experience with validation planning, execution, and reporting for quality control systems or equipment.</li><li>Experience with environmental monitoring programs and related quality oversight within manufacturing or laboratory settings.</li><li>Familiarity with CAPA management tools and electronic quality management systems.</li><li>Exposure to cell therapy or advanced biologics manufacturing processes and associated quality control testing.</li><li>Ability to contribute to continuous improvement initiatives, including process optimization and system enhancements.</li><li>Comfort working in a fast‑paced, entrepreneurial environment with evolving processes and responsibilities.</li><li>Demonstrated willingness to learn new technologies and approaches in support of innovative cell therapy development.</li><li>Approximately six‑month availability to provide maternity leave coverage in a contract or consultant capacity.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Sacramento, CA.Pay and BenefitsThe pay range for this position is $40.00 - $50.00/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 Sacramento,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: MicrobiologistJob DescriptionThis role focuses on supporting a growing animal health pharmaceutical facility by performing microbiology quality control activities in a QC laboratory. The microbiologist develops, evaluates, and validates compendial microbiology methods to support new product transfers to the site, including sterile injections, non-sterile liquid suspensions, and solid oral dose veterinary pharmaceutical products. The position collaborates closely with the microbiology QC team, project teams, and external customers as a technical subject matter expert, while working under the guidance of analytical development or quality control leadership.Responsibilities<ul><li>Perform method feasibility, development, and validation for compendial microbiology methods supporting new product transfers to the site.</li><li>Develop and validate microbiological methods for multiple product types, including sterile injection products, non-sterile liquid suspensions, and solid oral dose veterinary pharmaceutical drug products, as well as associated active pharmaceutical ingredients (APIs) and raw materials.</li><li>Author, execute, and complete method development and validation protocols, including writing and reviewing validation reports in alignment with established templates and standard operating procedures (SOPs).</li><li>Conduct sterility testing in accordance with USP &lt;71&gt;, including method validation for liquid injection products and sterile suspensions, with preferred use of isolator-based testing where applicable.</li><li>Perform endotoxin testing in accordance with USP &lt;85&gt;, including method validation for liquid injection products, raw materials, and sterile suspensions using kinetic chromogenic or turbidimetric methods and associated instrumentation.</li><li>Execute Microbial Limits Testing in accordance with USP &lt;61&gt; and &lt;62&gt;, including method validation for non-sterile liquids, pastes, suspensions, raw materials (solids and liquids), and bulk injection solutions.</li><li>Conduct subvisible particulate testing per USP &lt;788&gt; using light obscuration and microscopic methods to ensure compliance with particulate limits.</li><li>Perform media growth promotion testing and microbial identification to confirm suitability of culture media and accurately identify microorganisms as required.</li><li>Apply aseptic technique and cell culture practices to support microbiological assays and ensure contamination control in the laboratory.</li><li>Carry out bioburden and sterility-related testing activities as part of routine quality control and method validation programs.</li><li>Follow cGMP requirements and FDA 21 CFR 210/211 regulations in all laboratory operations, documentation, and quality control activities.</li><li>Collaborate closely with the microbiology QC team and cross-functional project teams to support timelines, resolve technical issues, and ensure successful method transfer and implementation.</li><li>Interface periodically with external customers as a technical subject matter expert to discuss methods, validation strategies, and testing results.</li><li>Work under the direction of analytical development or quality control management while receiving training from microbiologists on SOPs, equipment operation, and documentation standards.</li><li>Maintain accurate, complete, and compliant laboratory records, ensuring that all work aligns with established procedures and regulatory expectations.</li></ul>Essential Skills<ul><li>Bachelor’s degree in microbiology, biology, or a related scientific field.</li><li>4+ years of experience in a pharmaceutical manufacturing quality control role under cGMP, specifically aligned with FDA 21 CFR 210/211 requirements.</li><li>Hands-on experience in method development and validation, including authoring validation protocols, executing studies, and writing validation reports.</li><li>Demonstrated experience performing sterility testing in accordance with USP &lt;71&gt;, including method validation for liquid injection products and sterile suspensions, with preferred experience using isolators.</li><li>Experience performing endotoxin testing in accordance with USP &lt;85&gt;, including method validation for liquid injection products, raw materials, and sterile suspensions using kinetic chromogenic or turbidimetric methods and related instrumentation.</li><li>Experience with Microbial Limits Testing in accordance with USP &lt;61&gt; and &lt;62&gt;, including method validation for non-sterile liquids, pastes, suspensions, raw materials (solids and liquids), and bulk injection solutions.</li><li>Experience conducting subvisible particulate testing per USP &lt;788&gt; by light obscuration and microscopic methods.</li><li>Proficiency in media growth promotion testing and microbial identification techniques.</li><li>Demonstrated competency in aseptic technique and cell culture practices.</li><li>Practical experience performing bioburden, sterility, and related microbiological quality control tests.</li><li>Strong understanding of cGMP principles and quality control practices in a regulated pharmaceutical environment.</li><li>Ability to follow SOPs, operate laboratory equipment accurately, and maintain high-quality documentation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in an animal health or veterinary pharmaceutical environment is advantageous.</li><li>Prior experience serving as a technical subject matter expert and interfacing with external customers or partners is beneficial.</li><li>Familiarity with compendial microbiology methods and their application to sterile and non-sterile dosage forms.</li><li>Strong written and verbal communication skills for documenting methods, authoring reports, and collaborating with cross-functional teams.</li><li>Ability to work effectively in a small, collaborative microbiology team within a larger manufacturing and laboratory setting.</li><li>Detail-oriented mindset with strong problem-solving skills and the ability to troubleshoot microbiological methods and assays.</li></ul>Work EnvironmentThe role is based in a large manufacturing and laboratory facility that supports a growing animal health pharmaceutical operation. The microbiologist works closely with a small group of microbiologists in a quality control laboratory setting, using compendial microbiology methods and standard laboratory equipment to test sterile and non-sterile pharmaceutical products, APIs, and raw materials. The facility offers on-site amenities, including a gym, contributing to a supportive and health-conscious workplace. Standard work hours are Monday through Friday, 8:00 a.m. to 5:00 p.m., providing a stable daytime schedule in a professional laboratory and manufacturing environment.Job Type &amp; LocationThis is a Contract position based out of Shawnee, KS.Pay and BenefitsThe pay range for this position is $35.00 - $44.00/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 Shawnee,KS.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.

QC Microbiologist- Pharmaceutical

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP AN IMMEDIATE PHONE INTERVIEW!Description-Will be working doing bench testing which includes;-Sample prep-Wet Chemistry-Standard weighs-Dilutions-And over time will be trained on HPLC and GCThey will be trained in both the Oral Dose Solids and Nasals departments Conducts chemical and physical analyses in support of the development of a manufacturable multisource pharmaceutical product. Provides analytical support for the release of registration materials in support of regulatory submissions. Assists analytical method validation and transfer activities. Performs the assigned analytical tasks in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with cGXP's, and company practices and procedures. Follows work instructions, SOPs and company practices. Documents analytical activities and results accurately, in a timely manner and right-first time and maintains integrity of data. Follows written analytical procedures. Identifies execution challenges of analytical methods and support trouble shooting activities.Additional Skills &amp; QualificationsMUST - Bachelors in Science Field Prefer candidates with Bachelors in Chemistry or Biochemistry but will look at candidates with Biology, Microbiology, Pharmaceutical Science but must have strong Chem lab experience from school or outside of schoolMust have prior lab experience but can be from schoolStrongly prefer candidates that have lab experience outside of academiaMust be able to work in a team environment approach to accomplish tasks assigned. Must possess the ability to work on multiple tasks in a fast pace environment. Must possess good written and verbal communication skills. The candidate must have the ability to work with supervision using scientific judgment and professional competency.Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.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 Columbus,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.

QC Scientist I

We are hiring for an Entry-Level Pharmaceutical Scientist here in the Cincinnati, Ohio area! This is a long-term career opportunity and an ideal candidate will have a Bachelors Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline with chemistry laboratory coursework.Job DescriptionThe Pharmaceutical Scientist I is responsible for performing routine analyses and documentation of raw materials, in-process samples, calibrations, or projects within the QC Chemistry Laboratory of a large pharmaceutical company in the area. This role supports internal development and manufacturing operations by making detailed observations, reviewing, documenting, and communicating test results in a manner consistent with established standards.Responsibilities<ul><li>Conduct routine chemical and physical testing of raw materials using internally developed and compendial test methods.</li><li>Execute validated test methods for pharmaceutical raw materials to assess strength, impurities, identity, and characteristics using HPLC, GC, spectroscopy, and traditional wet chemical testing.</li><li>Recognize and report out-of-specification or unexpected results and non-routine analytical and product problems.</li><li>Perform daily instrument calibrations and verifications as required.</li><li>Clearly and accurately document the testing/analysis results and acquired data.</li><li>Record and report analysis results in accordance with prescribed lab procedures and systems.</li><li>Prepare test solutions, including media and mobile phases.</li><li>Clean and maintain work area and instrumentation.</li><li>Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and safety guidelines.</li><li>Maintain compliance status as required by company and facility standards.</li></ul>Qualifications:<ul><li>Bachelor’s degree in a science with strong chemistry coursework (preference for Chemistry or Biochemistry degrees, but not required)</li></ul>Job Type &amp; LocationThis is a Contract position based out of Cincinnati, OH.Pay and BenefitsThe pay range for this position is $18.00 - $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 Cincinnati,OH.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.

QC Supervisor – Raw MaterialsJob DescriptionThe QC Supervisor – Raw Materials manages the Raw Materials laboratory and a team of seven lab analysts, ensuring accurate, compliant, and timely testing of all incoming raw materials used in GMP manufacturing. This role provides hands-on leadership, oversees day-to-day laboratory operations, and ensures that testing meets regulatory, quality, and organizational standards while supporting staff development and operational excellence.Responsibilities<ul><li>Lead and manage the Raw Materials laboratory and a team of seven lab analysts, providing clear direction, coaching, and support.</li><li>Organize, schedule, and oversee testing of all incoming raw materials used in GMP manufacturing to ensure timely completion.</li><li>Ensure successful performance of raw material testing by monitoring workflow, prioritizing tasks, and aligning resources with testing demands.</li><li>Identify and remove obstacles that could delay completion of testing or assigned projects, ensuring on-time delivery of results.</li><li>Review testing documentation for accuracy, completeness, and compliance with Good Documentation Practices (GDP).</li><li>Review and revise raw material specifications, standard operating procedures (SOPs), and related documentation to maintain compliance and continuous improvement.</li><li>Train new hires on department processes, procedures, tools, and laboratory techniques to ensure consistent and compliant testing practices.</li><li>Lead investigations into deviations, nonconformances, or out-of-specification results related to raw material testing, and drive appropriate corrective and preventive actions.</li><li>Interact with auditors and clients during visits and tours, representing the laboratory and explaining processes, controls, and quality systems.</li><li>Oversee daily activities of the group to ensure adherence to quality standards, testing priorities, and maintenance of schedules.</li><li>Perform performance management for direct reports, including setting expectations, providing feedback, and supporting career development.</li><li>Review and approve documentation generated by the team, including test results, reports, and related records.</li><li>Drive organizational change within the team by developing and empowering staff, building effective and diverse teams, and fostering a culture of engagement and accountability.</li><li>Promote innovation, collaboration, transparency, and team effectiveness within the Raw Materials lab.</li><li>Manage timelines and coordinate work schedules for employees to align with testing needs and project deadlines.</li><li>Conduct or oversee verifications and qualifications for new testing methods and new client requirements related to raw materials.</li><li>Perform other job duties as assigned to support the broader quality control and manufacturing operations.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biological science, chemistry, or a related field is required.</li><li>Minimum of three years of experience leading people, such as in a team lead or supervisory capacity.</li><li>Minimum of three years of experience in raw materials testing or similar experience in the pharmaceutical industry, with a total of at least five years of relevant laboratory experience.</li><li>Experience with USP compendial raw material testing, including wet chemistry and titrations.</li><li>Hands-on experience performing wet chemistry testing and colorimetric titrations.</li><li>Experience with EP, JP, and USP testing for raw materials.</li><li>Pharmaceutical and GMP experience, including work in a cGMP environment.</li><li>Knowledge of GMP regulations and their application in a cGMP manufacturing setting.</li><li>Knowledge of raw materials sampling techniques and sampling plans.</li><li>Ability to drive functional, technical, and operational excellence within a laboratory environment.</li><li>Ability to manage timelines and coordinate work schedules for laboratory staff.</li><li>Strong ability to review and interpret laboratory data and documentation for accuracy and compliance.</li><li>Demonstrated leadership skills in developing and empowering staff, building effective teams, and driving engagement.</li><li>Strong communication skills to interact effectively with auditors, clients, and internal stakeholders.</li></ul>Additional Skills &amp; Qualifications<ul><li>At least one year of prior supervisory or lead experience is preferred.</li><li>Experience with analytical techniques such as HPLC is beneficial, with a preference for candidates who have raw materials USP testing experience.</li><li>Ability to inspire and foster innovation, collaboration, transparency, and team effectiveness.</li><li>Experience leading investigations into deviations and implementing corrective and preventive actions.</li><li>Ability to support staff in meeting their personal career goals while aligning with organizational objectives.</li><li>Strong organizational and problem-solving skills to identify and overcome obstacles to timely testing.</li><li>Experience participating in or supporting audits and client visits.</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 $42.00 - $48.55/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 1, 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.

QC Supervisor

QC Supervisor – Raw MaterialsJob DescriptionThe QC Supervisor – Raw Materials manages the Raw Materials laboratory and a team of seven lab analysts, ensuring accurate, compliant, and timely testing of all incoming raw materials used in GMP manufacturing. This role provides hands-on leadership, oversees day-to-day laboratory operations, and ensures that testing meets regulatory, quality, and organizational standards while supporting staff development and operational excellence.Responsibilities<ul><li>Lead and manage the Raw Materials laboratory and a team of seven lab analysts, providing clear direction, coaching, and support.</li><li>Organize, schedule, and oversee testing of all incoming raw materials used in GMP manufacturing to ensure timely completion.</li><li>Ensure successful performance of raw material testing by monitoring workflow, prioritizing tasks, and aligning resources with testing demands.</li><li>Identify and remove obstacles that could delay completion of testing or assigned projects, ensuring on-time delivery of results.</li><li>Review testing documentation for accuracy, completeness, and compliance with Good Documentation Practices (GDP).</li><li>Review and revise raw material specifications, standard operating procedures (SOPs), and related documentation to maintain compliance and continuous improvement.</li><li>Train new hires on department processes, procedures, tools, and laboratory techniques to ensure consistent and compliant testing practices.</li><li>Lead investigations into deviations, nonconformances, or out-of-specification results related to raw material testing, and drive appropriate corrective and preventive actions.</li><li>Interact with auditors and clients during visits and tours, representing the laboratory and explaining processes, controls, and quality systems.</li><li>Oversee daily activities of the group to ensure adherence to quality standards, testing priorities, and maintenance of schedules.</li><li>Perform performance management for direct reports, including setting expectations, providing feedback, and supporting career development.</li><li>Review and approve documentation generated by the team, including test results, reports, and related records.</li><li>Drive organizational change within the team by developing and empowering staff, building effective and diverse teams, and fostering a culture of engagement and accountability.</li><li>Promote innovation, collaboration, transparency, and team effectiveness within the Raw Materials lab.</li><li>Manage timelines and coordinate work schedules for employees to align with testing needs and project deadlines.</li><li>Conduct or oversee verifications and qualifications for new testing methods and new client requirements related to raw materials.</li><li>Perform other job duties as assigned to support the broader quality control and manufacturing operations.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biological science, chemistry, or a related field is required.</li><li>Minimum of three years of experience leading people, such as in a team lead or supervisory capacity.</li><li>Minimum of three years of experience in raw materials testing or similar experience in the pharmaceutical industry, with a total of at least five years of relevant laboratory experience.</li><li>Experience with USP compendial raw material testing, including wet chemistry and titrations.</li><li>Hands-on experience performing wet chemistry testing and colorimetric titrations.</li><li>Experience with EP, JP, and USP testing for raw materials.</li><li>Pharmaceutical and GMP experience, including work in a cGMP environment.</li><li>Knowledge of GMP regulations and their application in a cGMP manufacturing setting.</li><li>Knowledge of raw materials sampling techniques and sampling plans.</li><li>Ability to drive functional, technical, and operational excellence within a laboratory environment.</li><li>Ability to manage timelines and coordinate work schedules for laboratory staff.</li><li>Strong ability to review and interpret laboratory data and documentation for accuracy and compliance.</li><li>Demonstrated leadership skills in developing and empowering staff, building effective teams, and driving engagement.</li><li>Strong communication skills to interact effectively with auditors, clients, and internal stakeholders.</li></ul>Additional Skills &amp; Qualifications<ul><li>At least one year of prior supervisory or lead experience is preferred.</li><li>Experience with analytical techniques such as HPLC is beneficial, with a preference for candidates who have raw materials USP testing experience.</li><li>Ability to inspire and foster innovation, collaboration, transparency, and team effectiveness.</li><li>Experience leading investigations into deviations and implementing corrective and preventive actions.</li><li>Ability to support staff in meeting their personal career goals while aligning with organizational objectives.</li><li>Strong organizational and problem-solving skills to identify and overcome obstacles to timely testing.</li><li>Experience participating in or supporting audits and client visits.</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 $42.00 - $48.55/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 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.

QC Supervisor - Raw Materials Chemistry

Job Title: QC Supervisor – Raw Materials Job DescriptionThe QC Supervisor – Raw Materials manages the Raw Materials laboratory and a team of seven lab analysts, ensuring accurate, compliant, and timely testing of all incoming raw materials used in GMP manufacturing. This role provides hands-on leadership, oversees day-to-day laboratory operations, and ensures that testing meets regulatory, quality, and organizational standards while supporting staff development and operational excellence.Responsibilities<ul><li>Lead and manage the Raw Materials laboratory and a team of seven lab analysts, providing clear direction, coaching, and support.</li><li>Organize, schedule, and oversee testing of all incoming raw materials used in GMP manufacturing to ensure timely completion.</li><li>Ensure successful performance of raw material testing by monitoring workflow, prioritizing tasks, and aligning resources with testing demands.</li><li>Identify and remove obstacles that could delay completion of testing or assigned projects, ensuring on-time delivery of results.</li><li>Review testing documentation for accuracy, completeness, and compliance with Good Documentation Practices (GDP).</li><li>Review and revise raw material specifications, standard operating procedures (SOPs), and related documentation to maintain compliance and continuous improvement.</li><li>Train new hires on department processes, procedures, tools, and laboratory techniques to ensure consistent and compliant testing practices.</li><li>Lead investigations into deviations, nonconformances, or out-of-specification results related to raw material testing, and drive appropriate corrective and preventive actions.</li><li>Interact with auditors and clients during visits and tours, representing the laboratory and explaining processes, controls, and quality systems.</li><li>Oversee daily activities of the group to ensure adherence to quality standards, testing priorities, and maintenance of schedules.</li><li>Perform performance management for direct reports, including setting expectations, providing feedback, and supporting career development.</li><li>Review and approve documentation generated by the team, including test results, reports, and related records.</li><li>Drive organizational change within the team by developing and empowering staff, building effective and diverse teams, and fostering a culture of engagement and accountability.</li><li>Promote innovation, collaboration, transparency, and team effectiveness within the Raw Materials lab.</li><li>Manage timelines and coordinate work schedules for employees to align with testing needs and project deadlines.</li><li>Conduct or oversee verifications and qualifications for new testing methods and new client requirements related to raw materials.</li><li>Perform other job duties as assigned to support the broader quality control and manufacturing operations.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biological science, chemistry, or a related field is required.</li><li>Minimum of three years of experience leading people, such as in a team lead or supervisory capacity.</li><li>Minimum of three years of experience in raw materials testing or similar experience in the pharmaceutical industry, with a total of at least five years of relevant laboratory experience.</li><li>Experience with USP compendial raw material testing, including wet chemistry and titrations.</li><li>Hands-on experience performing wet chemistry testing and colorimetric titrations.</li><li>Experience with EP, JP, and USP testing for raw materials.</li><li>Pharmaceutical and GMP experience, including work in a cGMP environment.</li><li>Knowledge of GMP regulations and their application in a cGMP manufacturing setting.</li><li>Knowledge of raw materials sampling techniques and sampling plans.</li><li>Ability to drive functional, technical, and operational excellence within a laboratory environment.</li><li>Ability to manage timelines and coordinate work schedules for laboratory staff.</li><li>Strong ability to review and interpret laboratory data and documentation for accuracy and compliance.</li><li>Demonstrated leadership skills in developing and empowering staff, building effective teams, and driving engagement.</li><li>Strong communication skills to interact effectively with auditors, clients, and internal stakeholders.</li></ul>Additional Skills &amp; Qualifications<ul><li>At least one year of prior supervisory or lead experience is preferred.</li><li>Experience with analytical techniques such as HPLC is beneficial, with a preference for candidates who have raw materials USP testing experience.</li><li>Ability to inspire and foster innovation, collaboration, transparency, and team effectiveness.</li><li>Experience leading investigations into deviations and implementing corrective and preventive actions.</li><li>Comfort working with a range of experience levels within the team, from junior analysts to senior scientists.</li><li>Ability to support staff in meeting their personal career goals while aligning with organizational objectives.</li><li>Strong organizational and problem-solving skills to identify and overcome obstacles to timely testing.</li><li>Experience participating in or supporting audits and client visits.</li></ul>Work EnvironmentThe role is based in a laboratory environment focused on raw materials testing within a cGMP manufacturing setting. You will work closely with a team of seven lab analysts whose experience levels vary, including one senior scientist and several more junior analysts. The lab conducts compendial raw material testing, including USP, EP, and JP methods, wet chemistry, titrations, and related pharmaceutical quality control activities. The environment emphasizes quality, compliance, collaboration, and continuous improvement, offering the opportunity to contribute to meaningful work such as supporting the development of therapies, protecting the environment, or ensuring food safety, while supporting your professional growth and career goals.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 $42.00 - $48.55/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 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: QC Supervisor – Raw MaterialsJob DescriptionThe QC Supervisor – Raw Materials manages the Raw Materials laboratory and a team of seven lab analysts, ensuring accurate, compliant, and timely testing of all incoming raw materials used in GMP manufacturing. This role provides hands-on leadership, oversees day-to-day laboratory operations, and ensures that testing meets regulatory, quality, and organizational standards while supporting staff development and operational excellence.Responsibilities<ul><li>Lead and manage the Raw Materials laboratory and a team of seven lab analysts, providing clear direction, coaching, and support.</li><li>Organize, schedule, and oversee testing of all incoming raw materials used in GMP manufacturing to ensure timely completion.</li><li>Ensure successful performance of raw material testing by monitoring workflow, prioritizing tasks, and aligning resources with testing demands.</li><li>Identify and remove obstacles that could delay completion of testing or assigned projects, ensuring on-time delivery of results.</li><li>Review testing documentation for accuracy, completeness, and compliance with Good Documentation Practices (GDP).</li><li>Review and revise raw material specifications, standard operating procedures (SOPs), and related documentation to maintain compliance and continuous improvement.</li><li>Train new hires on department processes, procedures, tools, and laboratory techniques to ensure consistent and compliant testing practices.</li><li>Lead investigations into deviations, nonconformances, or out-of-specification results related to raw material testing, and drive appropriate corrective and preventive actions.</li><li>Interact with auditors and clients during visits and tours, representing the laboratory and explaining processes, controls, and quality systems.</li><li>Oversee daily activities of the group to ensure adherence to quality standards, testing priorities, and maintenance of schedules.</li><li>Perform performance management for direct reports, including setting expectations, providing feedback, and supporting career development.</li><li>Review and approve documentation generated by the team, including test results, reports, and related records.</li><li>Drive organizational change within the team by developing and empowering staff, building effective and diverse teams, and fostering a culture of engagement and accountability.</li><li>Promote innovation, collaboration, transparency, and team effectiveness within the Raw Materials lab.</li><li>Manage timelines and coordinate work schedules for employees to align with testing needs and project deadlines.</li><li>Conduct or oversee verifications and qualifications for new testing methods and new client requirements related to raw materials.</li><li>Perform other job duties as assigned to support the broader quality control and manufacturing operations.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biological science, chemistry, or a related field is required.</li><li>Minimum of three years of experience leading people, such as in a team lead or supervisory capacity.</li><li>Minimum of three years of experience in raw materials testing or similar experience in the pharmaceutical industry, with a total of at least five years of relevant laboratory experience.</li><li>Experience with USP compendial raw material testing, including wet chemistry and titrations.</li><li>Hands-on experience performing wet chemistry testing and colorimetric titrations.</li><li>Experience with EP, JP, and USP testing for raw materials.</li><li>Pharmaceutical and GMP experience, including work in a cGMP environment.</li><li>Knowledge of GMP regulations and their application in a cGMP manufacturing setting.</li><li>Knowledge of raw materials sampling techniques and sampling plans.</li><li>Ability to drive functional, technical, and operational excellence within a laboratory environment.</li><li>Ability to manage timelines and coordinate work schedules for laboratory staff.</li><li>Strong ability to review and interpret laboratory data and documentation for accuracy and compliance.</li><li>Demonstrated leadership skills in developing and empowering staff, building effective teams, and driving engagement.</li><li>Strong communication skills to interact effectively with auditors, clients, and internal stakeholders.</li></ul>Additional Skills &amp; Qualifications<ul><li>At least one year of prior supervisory or lead experience is preferred.</li><li>Experience with analytical techniques such as HPLC is beneficial, with a preference for candidates who have raw materials USP testing experience.</li><li>Ability to inspire and foster innovation, collaboration, transparency, and team effectiveness.</li><li>Experience leading investigations into deviations and implementing corrective and preventive actions.</li><li>Comfort working with a range of experience levels within the team, from junior analysts to senior scientists.</li><li>Ability to support staff in meeting their personal career goals while aligning with organizational objectives.</li><li>Strong organizational and problem-solving skills to identify and overcome obstacles to timely testing.</li><li>Experience participating in or supporting audits and client visits.</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 $42.00 - $48.55/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 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: QC Supervisor – Raw MaterialsJob DescriptionThe QC Supervisor – Raw Materials manages the Raw Materials laboratory and a team of seven lab analysts, ensuring accurate, compliant, and timely testing of all incoming raw materials used in GMP manufacturing. This role provides hands-on leadership, oversees day-to-day laboratory operations, and ensures that testing meets regulatory, quality, and organizational standards while supporting staff development and operational excellence.Responsibilities<ul><li>Lead and manage the Raw Materials laboratory and a team of seven lab analysts, providing clear direction, coaching, and support.</li><li>Organize, schedule, and oversee testing of all incoming raw materials used in GMP manufacturing to ensure timely completion.</li><li>Ensure successful performance of raw material testing by monitoring workflow, prioritizing tasks, and aligning resources with testing demands.</li><li>Identify and remove obstacles that could delay completion of testing or assigned projects, ensuring on-time delivery of results.</li><li>Review testing documentation for accuracy, completeness, and compliance with Good Documentation Practices (GDP).</li><li>Review and revise raw material specifications, standard operating procedures (SOPs), and related documentation to maintain compliance and continuous improvement.</li><li>Train new hires on department processes, procedures, tools, and laboratory techniques to ensure consistent and compliant testing practices.</li><li>Lead investigations into deviations, nonconformances, or out-of-specification results related to raw material testing, and drive appropriate corrective and preventive actions.</li><li>Interact with auditors and clients during visits and tours, representing the laboratory and explaining processes, controls, and quality systems.</li><li>Oversee daily activities of the group to ensure adherence to quality standards, testing priorities, and maintenance of schedules.</li><li>Perform performance management for direct reports, including setting expectations, providing feedback, and supporting career development.</li><li>Review and approve documentation generated by the team, including test results, reports, and related records.</li><li>Drive organizational change within the team by developing and empowering staff, building effective and diverse teams, and fostering a culture of engagement and accountability.</li><li>Promote innovation, collaboration, transparency, and team effectiveness within the Raw Materials lab.</li><li>Manage timelines and coordinate work schedules for employees to align with testing needs and project deadlines.</li><li>Conduct or oversee verifications and qualifications for new testing methods and new client requirements related to raw materials.</li><li>Perform other job duties as assigned to support the broader quality control and manufacturing operations.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biological science, chemistry, or a related field is required.</li><li>Minimum of three years of experience leading people, such as in a team lead or supervisory capacity.</li><li>Minimum of three years of experience in raw materials testing or similar experience in the pharmaceutical industry, with a total of at least five years of relevant laboratory experience.</li><li>Experience with USP compendial raw material testing, including wet chemistry and titrations.</li><li>Hands-on experience performing wet chemistry testing and colorimetric titrations.</li><li>Experience with EP, JP, and USP testing for raw materials.</li><li>Pharmaceutical and GMP experience, including work in a cGMP environment.</li><li>Knowledge of GMP regulations and their application in a cGMP manufacturing setting.</li><li>Knowledge of raw materials sampling techniques and sampling plans.</li><li>Ability to drive functional, technical, and operational excellence within a laboratory environment.</li><li>Ability to manage timelines and coordinate work schedules for laboratory staff.</li><li>Strong ability to review and interpret laboratory data and documentation for accuracy and compliance.</li><li>Demonstrated leadership skills in developing and empowering staff, building effective teams, and driving engagement.</li><li>Strong communication skills to interact effectively with auditors, clients, and internal stakeholders.</li></ul>Additional Skills &amp; Qualifications<ul><li>At least one year of prior supervisory or lead experience is preferred.</li><li>Experience with analytical techniques such as HPLC is beneficial, with a preference for candidates who have raw materials USP testing experience.</li><li>Ability to inspire and foster innovation, collaboration, transparency, and team effectiveness.</li><li>Experience leading investigations into deviations and implementing corrective and preventive actions.</li><li>Comfort working with a range of experience levels within the team, from junior analysts to sr scientists.</li><li>Ability to support staff in meeting their personal career goals while aligning with organizational objectives.</li><li>Strong organizational and problem-solving skills to identify and overcome obstacles to timely testing.</li><li>Experience participating in or supporting audits and client visits.</li></ul>Work EnvironmentssThe role is based in a laboratory environment focused on raw materials testing within a cGMP manufacturing setting. You will work closely with a team of seven lab analysts whose experience levels vary, including one sr scientist and several more junior analysts. The lab conducts compendial raw material testing, including USP, EP, and JP methods, wet chemistry, titrations, and related pharmaceutical quality control activities. The environment emphasizes quality, compliance, collaboration, and continuous improvement, offering the opportunity to contribute to meaningful work such as supporting the development of therapies, protecting the environment, or ensuring food safety, while supporting your professional growth and career goals.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 $42.00 - $48.55/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 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: QMS Supervisor - Medical Devices Job DescriptionThe Quality Management Systems (QMS) Supervisor oversees the development, implementation, and continuous improvement of the organization’s Quality Management System to ensure full compliance with applicable regulatory and industry standards. This role partners closely with cross-functional teams to foster a strong culture of quality, maintain audit readiness, and drive continuous improvement initiatives across the organization. Reporting into senior Quality leadership, the QMS Supervisor plays a hands-on role in audit management, CAPA oversight, document control, and QMS performance monitoring, while serving as a key resource for quality training and compliance guidance.Responsibilities<ul><li>Own and maintain the Quality Management System structure, including policies, procedures, standard operating procedures (SOPs), and work instructions, ensuring alignment with regulatory requirements and organizational objectives.</li><li>Support and lead internal and external audits, including registrar, customer, supplier, and regulatory audits, covering audit preparation, hosting, and response execution.</li><li>Lead root cause investigations for nonconformances, deviations, and customer complaints, and develop, implement, and verify effective Corrective and Preventive Actions (CAPAs).</li><li>Drive continuous improvement initiatives using Lean principles, statistical tools, and data analysis to enhance product quality and operational efficiency.</li><li>Oversee electronic Quality Management Systems (eQMS) and document control processes to ensure data accuracy, robust version control, and ongoing compliance.</li><li>Develop, track, and present quality metrics and key performance indicators (KPIs) to leadership to support informed decision-making and strategic planning.</li><li>Deliver QMS, Good Manufacturing Practice (GMP), and compliance training to cross-functional personnel to reinforce quality awareness and accountability throughout the organization.</li><li>Ensure alignment and consistency of quality programs and processes across all relevant departments and functions.</li><li>Regularly review, assess, and improve quality processes to enhance effectiveness, manage risk, and control costs within the quality system.</li><li>Collaborate closely with cross-functional teams, including manufacturing, R&amp;D, and operations, to support compliance-driven activities and initiatives.</li></ul>Essential Skills<ul><li>Minimum of 5 years of experience in a Quality Management Systems or Quality Assurance leadership role within a regulated industry.</li><li>Strong working knowledge of quality management standards and audit processes, including ISO-based quality system frameworks.</li><li>Proven experience leading CAPA investigations, including root cause analysis, development of corrective and preventive actions, and verification of effectiveness.</li><li>Hands-on experience administering and maintaining an electronic Quality Management System (eQMS) platform.</li><li>Expertise in document control systems, including change management and training record management in a regulated environment.</li><li>Ability to analyze quality data, identify trends, and implement sustainable corrective and preventive actions based on data-driven insights.</li><li>Demonstrated experience in quality assurance for medical devices, including exposure to spine, neurology, or implantable device products.</li><li>Experience with internal and external audits within a quality-regulated environment.</li><li>Strong understanding of regulatory affairs and quality assurance practices in regulated industries.</li><li>Excellent written and verbal communication skills, with the ability to interface effectively with auditors, customers, and internal stakeholders at all levels.</li><li>Demonstrated ability to influence cross-functional teams and lead through collaboration without direct authority.</li><li>Strong organizational skills and high attention to detail, particularly in managing regulated documentation and records.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in the medical device industry.</li><li>Knowledge of FDA Quality System Regulation (QSR) and Good Manufacturing Practice (GMP) requirements.</li><li>Certified Internal Auditor or equivalent certification in ISO-based quality management systems.</li><li>ASQ Certified Quality Auditor (CQA) or Certified Quality Engineer (CQE) credentials.</li><li>Lean Six Sigma Green Belt or Black Belt certification or training.</li><li>Experience supporting manufacturing, research and development (R&amp;D), and operations teams within a compliance-driven environment.</li><li>Familiarity with quality management standards such as AS9100 and ISO 9001.</li><li>Background in quality management for specialized medical device areas such as spine, neurology, or implantable devices.</li></ul>Work EnvironmentThis role is 100% office-based in a cubicle work environment, providing a structured and professional setting focused on quality and compliance activities. The position centers on the use of electronic Quality Management Systems and other office-based tools to manage documentation, audits, metrics, and training. The work environment supports collaboration with cross-functional teams, including quality, manufacturing, R&amp;D, and operations. Eligible employees may receive a discretionary year-end bonus, which is not tied to individual performance.Job Type &amp; LocationThis is a Permanent position based out of Baldwin, NY.Pay and BenefitsThe pay range for this position is $95000.00 - $105000.00/yr.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 - They match 25% of 1%, up to 4%.
 • 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) - 18 total days of PTO + 13 holidaysWorkplace TypeThis is a fully onsite position in Baldwin,NY.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.

QMS Supervisor - Medical Devices

Job TitleQuality InspectorJob DescriptionAs a Quality Inspector, you will perform a variety of parts and product inspections to ensure they meet company and customer requirements. You will be responsible for inspecting incoming sub out parts, documenting inspection results, and creating reports for customers.Responsibilities<ul><li>Perform parts and product inspections to meet company and customer standards.</li><li>Inspect incoming sub out parts.</li><li>Document inspection results through written records or photos.</li><li>Gather data and create reports for customers.</li><li>Communicate quality discrepancies to shop supervisors.</li><li>Maintain material certifications and inspection documentation.</li><li>Maintain calibration control for all IMTE inventory.</li><li>Perform inspections to ISO standards.</li><li>Notify management of need for Certified Welding Inspector (CWI).</li><li>Use basic measurement tools such as combination square, protractor, and caliper.</li><li>Assist with the sub out process by requesting purchase orders, tagging, and documenting counts.</li><li>Label nonconforming parts.</li><li>Read blueprints to ensure fabricated products meet specifications.</li><li>Follow all safety procedures.</li><li>Perform other responsibilities as assigned by the supervisor.</li></ul>Skills and Qualifications Required<ul><li>An associate degree in Quality Control Technology or 3+ years of proven inspection experience.</li><li>Minimum 2+ years of experience as an inspector in a close tolerance, custom metal manufacturing business.</li><li>Experience in a metal forming, machining, or welding environment is preferred.</li><li>Knowledge of metals and raw materials, production processes, quality control, and manufacturing costs is advantageous.</li><li>General machining and welding knowledge is a plus.</li></ul>Work EnvironmentThe role involves working in a metal manufacturing environment, with a focus on maintaining safety procedures and using various precision measurement tools. The position requires adherence to ISO standards and may involve reading blueprints to ensure product specifications are met.Job Type &amp; LocationThis is a Contract to Hire position based out of Green Bay, WI.Pay and BenefitsThe pay range for this position is $28.00 - $30.00/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 Green Bay,WI.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 INSPECTOR

Job TitleQuality InspectorJob DescriptionAs a Quality Inspector, you will perform a variety of parts and product inspections to ensure they meet company and customer requirements. You will be responsible for inspecting incoming sub out parts, documenting inspection results, and creating reports for customers.Responsibilities<ul><li>Perform parts and product inspections to meet company and customer standards.</li><li>Inspect incoming sub out parts.</li><li>Document inspection results through written records or photos.</li><li>Gather data and create reports for customers.</li><li>Communicate quality discrepancies to shop supervisors.</li><li>Maintain material certifications and inspection documentation.</li><li>Maintain calibration control for all IMTE inventory.</li><li>Perform inspections to ISO standards.</li><li>Notify management of need for Certified Welding Inspector (CWI).</li><li>Use basic measurement tools such as combination square, protractor, and caliper.</li><li>Assist with the sub out process by requesting purchase orders, tagging, and documenting counts.</li><li>Label nonconforming parts.</li><li>Read blueprints to ensure fabricated products meet specifications.</li><li>Follow all safety procedures.</li><li>Perform other responsibilities as assigned by the supervisor.</li></ul>Skills and Qualifications Required<ul><li>An associate degree in Quality Control Technology or 3+ years of proven inspection experience.</li><li>Minimum 2+ years of experience as an inspector in a close tolerance, custom metal manufacturing business.</li><li>Experience in a metal forming, machining, or welding environment is preferred.</li><li>Knowledge of metals and raw materials, production processes, quality control, and manufacturing costs is advantageous.</li><li>General machining and welding knowledge is a plus.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Green Bay, WI.Pay and BenefitsThe pay range for this position is $28.00 - $30.00/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 Green Bay,WI.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.

Job Title: Quality Assurance/Quality Control Manager - ConstructionJob DescriptionWe are seeking a dedicated Quality Assurance/Quality Control Manager to oversee all QA/QC activities for the construction of workforce housing supporting a large-scale data center project. The successful candidate will ensure all construction work complies with project specifications, contract requirements, applicable codes, and quality standards, while fostering a culture of quality and continuous improvement across the project site.Responsibilities<ul><li>Develop, implement, and maintain the project's QA/QC program.</li><li>Review construction documents, specifications, submittals, RFIs, and shop drawings for compliance.</li><li>Conduct daily field inspections and quality audits across all phases of construction.</li><li>Coordinate with Superintendents, Project Managers, Engineers, Owners, and Subcontractors to ensure quality expectations are met.</li><li>Manage inspection and test plans (ITPs), material inspections, and quality documentation.</li><li>Track deficiencies, non-conformance reports (NCRs), corrective actions, and punch lists.</li><li>Perform root-cause investigations and implement corrective and preventive measures.</li><li>Verify work is completed in accordance with applicable building codes, project specifications, and safety requirements.</li><li>Coordinate third-party inspections, testing agencies, and commissioning activities.</li><li>Review and approve quality-related turnover packages and closeout documentation.</li><li>Maintain detailed quality records and reports for project leadership and client representatives.</li><li>Support project turnover and owner acceptance processes.</li><li>Mentor field teams and subcontractors on quality standards and best practices.</li></ul>Essential Skills<ul><li>7+ years of QA/QC experience in commercial, industrial, mission-critical, manufacturing, or large-scale construction projects.</li><li>Experience managing QA/QC programs on projects valued at $20M+.</li><li>Experience overseeing subcontractor quality performance.</li><li>Strong background in construction management, quality assurance, and quality control.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of modular buildings, workforce housing, data centers, or mission-critical facilities preferred.</li><li>Experience with project closeout, commissioning support, and turnover documentation.</li><li>Certified Construction Quality Manager (CQM-C).</li><li>ASQ Certified Quality Engineer (CQE).</li><li>OSHA 30.</li><li>CCM (Certified Construction Manager).</li><li>PMP Certification.</li></ul>Work EnvironmentThis role requires working on a remote construction site, often in isolated locations. The work environment necessitates adherence to safety standards and appropriate attire for construction settings. The position involves coordination with various stakeholders and managing comprehensive documentation and reporting.Job Type &amp; LocationThis is a Contract position based out of Mobeetie, TX.Pay and BenefitsThe pay range for this position is $45.00 - $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 Mobeetie,TX.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.

Qa/qc Manager

Job Title: QA/QC Specialist – Mechanical Construction Job DescriptionThis project-based QA/QC Specialist role supports large-scale mechanical systems on a semiconductor facility project. You will ensure that mechanical, process piping, and structural fabrications comply with ASME/AWS codes, project specifications, and quality standards. The position focuses on managing site-specific quality plans, performing inspections and audits, overseeing documentation, and supporting subcontractor quality to deliver safe, high-quality outcomes. The role offers the potential to transition into a long-term position within an employee-owned organization that values autonomy, professional growth, and long-tenured careers.Responsibilities<ul><li>Ensure mechanical, process piping, and structural fabrications meet ASME/AWS codes, project specifications, and established quality standards.</li><li>Develop, implement, and manage site-specific quality plans for a large semiconductor project.</li><li>Perform QA/QC inspections and audits on mechanical and piping systems to verify compliance with design and regulatory requirements.</li><li>Conduct and document QC testing for large systems, including pressure testing, and ensure proper QA/QC sign-off for completed work.</li><li>Review and interpret drawings, logs, and P&amp;ID documents to validate installation quality and system integrity.</li><li>Control and maintain quality-related documentation, including inspection reports, test records, certifications, and sign-offs.</li><li>Supervise and monitor subcontractor quality activities to ensure adherence to project quality plans and standards.</li><li>Promote and support a strong safety culture with a focus on zero injuries while maintaining high-quality outcomes.</li><li>Collaborate with construction management, engineering, and field teams to resolve quality issues and implement corrective actions.</li><li>Utilize Microsoft Office and other company software tools such as Word, Excel, Bluebeam, ACC Build, and Navisworks to prepare reports, track quality metrics, and manage documentation.</li><li>Apply knowledge of different welding processes and high purity piping systems to evaluate workmanship and material compliance.</li><li>Coordinate QA/QC activities related to semiconductor, data center, and pharmaceutical-type environments, including process piping and high purity systems.</li><li>Work independently with minimal supervision while managing multiple QA/QC tasks in a fast-paced construction environment.</li><li>Support smart completions and related systems, when applicable, to ensure accurate tracking of construction and quality status.</li><li>Contribute to a culture of continuous improvement by identifying opportunities to enhance quality processes and documentation.</li></ul>Essential Skills<ul><li>Minimum 3+ years of experience in a QA/QC role within the mechanical construction industry.</li><li>Level 2 certification in a relevant QA/QC or inspection discipline.</li><li>Experience working on semiconductor and/or data center projects.</li><li>Strong understanding of mechanical systems, process piping, and structural fabrications in a construction environment.</li><li>Ability to read and comprehend logs, drawings, and P&amp;ID documents.</li><li>Understanding of pressure testing procedures and requirements.</li><li>Knowledge of different welding processes and their quality standards.</li><li>Familiarity with piping and component material standards, including certification documentation for high purity piping systems.</li><li>Proficiency in Microsoft Office, including Word and Excel.</li><li>Proficiency with company software tools such as Bluebeam, ACC Build, and Navisworks.</li><li>Ability to work effectively under pressure in a fast-paced project environment.</li><li>Ability to work with minimal supervision and take ownership of assigned QA/QC tasks.</li><li>Availability to work overtime as required by project needs.</li><li>Ability to work at heights as needed on a construction site.</li><li>Physical ability to access tight or confined spaces safely.</li></ul>Additional Skills &amp; Qualifications<ul><li>CWI (Certified Welding Inspector) certification.</li><li>Current eye test suitable for inspection duties.</li><li>Experience using smart completions or similar construction completion systems.</li><li>Background in construction quality management for semiconductor, data center, or pharmaceutical projects.</li><li>Experience coordinating with general contractors and multiple subcontractors on complex projects.</li><li>Strong communication skills to interface with field teams, subcontractors, and project leadership.</li><li>Demonstrated commitment to safety and quality in a construction environment.</li><li>Interest in long-term career growth within an employee-owned organization that values continuity and productivity.</li></ul>Work EnvironmentThis role is fully onsite at a large semiconductor project in Boise, ID. The current schedule follows a 60/60/50 work pattern, with workdays typically running Monday through Saturday, starting at 6:00 a.m. and consisting of 10-hour shifts. The position is project-based and field-focused, and there is no dedicated physical office in Boise for this role. You will work on an active construction site alongside a primary general contractor and multiple trade partners, using tools such as Microsoft Office, Bluebeam, ACC Build, and Navisworks to support QA/QC activities. The environment involves working at heights and in tight or confined spaces, as well as performing inspections on mechanical, process piping, and structural systems. The culture emphasizes autonomy, accountability, and collaboration, with an employee-owned structure that encourages long-term engagement and pride in quality work. Per diem support is provided for eligible candidates while working on this project.Job Type &amp; LocationThis is a Contract to Hire position based out of Boise, ID.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 Boise,ID.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.

Qa/qc Specialist

<h2 style="text-align:center;">Batching Documentation Technician</h2>Job Description Join a dynamic team dedicated to ensuring food safety and quality through rigorous laboratory and production support functions. As a QC Lab Technician, you will perform microbiological and analytical testing to support our Pre-Operation sanitation and HACCP program, ensuring the highest standards of product quality and safety. Responsibilities<ul><li>Verify for correctness and accuracy all batching kits prior to being shipping to the main plant. Attention to detail and good math skills are required for this position.</li><li>Assists with inventory accuracy. </li><li>Assists in the coordination, monitoring and testing of all Vendors to meet Quality/Compliance expectations for products they provide.</li><li>Assists in working with manufacturing in designing and enhancing quality management systems to facilitate overall regulatory compliance.</li><li>Assists the Batching Compliance Analyst Lead in serving as liaison with all compliance issues.</li><li>Verification of ingredient quantities during kit stage in DC batching area. Must be able to lift 55 lbs. on a regular basis.</li><li>Organoleptic analysis of all supplied ingredients.</li><li>Report any non-conformance</li><li>Know all quality standards and expectations of position</li><li>Report any waste or poor conservation practices</li><li>Continuously looking for improved practices and processes in your position, and contributing these ideas to your immediate supervisor</li><li>Know all safety requirements of position prior to starting any job.</li><li>Follow all safety rules and procedures established by the company.</li><li>Performs all other duties as assigned or required by supervisor/customer.</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma or equivalent</li><li>Knowledge working in Outlook, Microsoft Office, Word, and Excel</li><li>Strong attention to detail</li><li>Good at multitasking</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of St. Cloud, MN.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 St. Cloud,MN.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.

Qa/qc Technician

Description
					Purpose of this Role:
The Quality and Compliance Lead is responsible for establishing and maintaining a fit-for
purpose quality system to support the development, launch, and commercialization of
agricultural products manufactured through external partners. This role ensures
compliance with regulatory requirements, oversees quality performance across CMOs and
tolling partners, and drives continuous improvement initiatives to safeguard product
quality, reliability, and customer satisfaction.
The position serves as the primary quality interface between the company and external
manufacturing, formulation, packaging, and logistics partners.
.
Key Responsibilties:
External Manufacturing Quality Management
▪
Develop and maintain the company's Quality Management System (QMS) appropriate for a virtual manufacturing environment.
▪
Establish quality standards, specifications, and release requirements for products manufactured by CMOs and tolling partners.
▪
Qualify, onboard, and periodically assess contract manufacturers, formulators, packagers, and critical suppliers.
▪
Define and implement supplier quality agreements and performance expectations.
▪
Monitor manufacturing performance through KPIs, scorecards, and regular business reviews.
▪
Support technology transfer, scale-up, validation, and commercial launch activities.
Compliance and Risk Management
▪
Ensure products and manufacturing operations comply with applicable regulatory requirements, customer specifications, and company standards.
▪
Maintain audit readiness and coordinate supplier audits, qualification assessments, and compliance reviews.
▪
Lead investigations related to deviations, complaints, out-of-specification results, and non-conformances.
▪
Drive CAPA implementation and verify effectiveness of corrective actions.
▪
Oversee change control processes to assess impacts on product quality, regulatory compliance, and supply continuity.
▪
Identify and mitigate quality and compliance risks across the external manufacturing network.
Product Launch Support
▪
Partner with Regulatory, Product Development, Supply Chain, and Commercial teams to support successful product introductions.
▪
Establish quality requirements for new products and ensure manufacturing readiness prior to launch.
▪
Participate in process optimization efforts to improve product consistency, manufacturability, and cost competitiveness.
▪
Support inventory disposition decisions and product release processes.
Continuous Improvement
▪
Develop supplier improvement plans and collaborate with manufacturing partners to enhance performance.
▪
Analyze quality trends and implement preventive measures to reduce risk and variability.
▪
Promote a culture of quality throughout the organization and across the external partner network.
Qualifications
▪
Bachelor's degree in Agriculture, Chemistry, Engineering, Biology, Pharmacy, or related discipline; advanced degree preferred.
▪
8+ years of experience in Quality Assurance, Compliance, Manufacturing, or Supplier Quality within agriculture, biologicals, crop protection, biotechnology, or specialty chemicals.
▪
Experience managing quality systems in outsourced or virtual manufacturing environments.
▪
Demonstrated experience working with CMOs, toll manufacturers, formulators, and global supply partners.
▪
Knowledge of supplier qualification, audits, quality agreements, CAPA, change management, and product launch processes.
▪
Strong communication, influence, and relationship management skills.
▪
Ability to operate effectively in a fast-paced, resource-constrained startup environment.
Key Competencies
▪
Supplier Quality Management
▪
Influencing Without Authority
▪
Risk Assessment and Mitigation
▪
Change Management
▪
CAPA and Root Cause Analysis
▪
Technology Transfer and Product Launch Support
▪
Agility and Execution in a Startup Environment
▪
Cross-Functional Collaboration
▪
Continuous Improvement
▪
Strong Communication and Stakeholder Management
Sucess Factors
▪
Builds strong partnerships with external manufacturers and suppliers.
▪
Anticipates and mitigates quality risks before they impact customers or supply.
▪
Balances compliance rigor with agility needed in a growing organization.
▪
Drives accountability and continuous improvement across the manufacturing network.
					 					Skills
					QMS, CMO, Chemistry, CAPA, quality assurance
					 					Top Skills Details
					QMS,CMO,Chemistry,CAPA,quality assurance
					 					Additional Skills &amp; Qualifications
					Qualifications
▪
Bachelor's degree in Agriculture, Chemistry, Engineering, Biology, Pharmacy, or related discipline; advanced degree preferred.
▪
8+ years of experience in Quality Assurance, Compliance, Manufacturing, or Supplier Quality within agriculture, biologicals, crop protection, biotechnology, or specialty chemicals.
▪
Experience managing quality systems in outsourced or virtual manufacturing environments.
▪
Demonstrated experience working with CMOs, toll manufacturers, formulators, and global supply partners.
▪
Knowledge of supplier qualification, audits, quality agreements, CAPA, change management, and product launch processes.
▪
Strong communication, influence, and relationship management skills.
▪
Ability to operate effectively in a fast-paced, resource-constrained startup environment.
					 					Experience Level
					Expert Level
					 Job Type &amp; LocationThis is a Contract to Hire position based out of Santa Monica, CA.Pay and BenefitsThe pay range for this position is $57.60 - $63.00/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 remote position.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 & Compliance Lead

Build the quality systems that enable the next generation of agricultural innovation. Join a fast-growing startup where you'll lead supplier quality, compliance, and continuous improvement across a global manufacturing network.Job Title: Quality &amp; Compliance LeadJob DescriptionThe Quality &amp; Compliance Lead establishes and maintains a robust, fit-for-purpose quality management system to support the development, launch, and commercialization of agricultural products manufactured through external partners. This role serves as the primary quality interface with contract manufacturers, tolling partners, formulators, packagers, and logistics providers, ensuring regulatory compliance, consistent product quality, and reliable supply. The position drives continuous improvement across the external manufacturing network while balancing compliance rigor with the agility required in a fast-paced, resource-constrained startup environment.Responsibilities<ul><li>Develop and maintain a comprehensive Quality Management System (QMS) tailored to a virtual and outsourced manufacturing environment.</li><li>Establish clear quality standards, specifications, and release requirements for products manufactured by contract manufacturing organizations (CMOs) and tolling partners.</li><li>Qualify, onboard, and periodically assess contract manufacturers, formulators, packagers, and critical suppliers to ensure they meet quality and compliance expectations.</li><li>Define, implement, and maintain supplier quality agreements, including performance expectations and roles and responsibilities.</li><li>Monitor manufacturing performance using key performance indicators, scorecards, and regular business reviews, and address gaps proactively.</li><li>Support technology transfer, scale-up, validation, and commercial launch activities for new and existing products.</li><li>Ensure products and manufacturing operations comply with applicable regulatory requirements, customer specifications, and internal company standards.</li><li>Maintain a state of audit readiness and coordinate supplier audits, qualification assessments, and compliance reviews.</li><li>Lead investigations related to deviations, customer complaints, out-of-specification results, and non-conformances, ensuring thorough root cause analysis.</li><li>Drive corrective and preventive actions (CAPA), verify the effectiveness of implemented actions, and embed lessons learned into procedures and practices.</li><li>Oversee change control processes to assess and manage impacts on product quality, regulatory compliance, and supply continuity.</li><li>Identify, assess, and mitigate quality and compliance risks across the external manufacturing network using structured risk assessment and mitigation approaches.</li><li>Partner with Regulatory, Product Development, Supply Chain, and Commercial teams to support successful product introductions and lifecycle management.</li><li>Establish quality requirements for new products and ensure manufacturing readiness and robust controls are in place prior to launch.</li><li>Participate in process optimization initiatives to improve product consistency, manufacturability, and cost competitiveness.</li><li>Support inventory disposition decisions and product release processes, ensuring timely and compliant supply to customers.</li><li>Develop and execute supplier improvement plans and collaborate with manufacturing partners to enhance quality, reliability, and service.</li><li>Analyze quality trends, identify systemic issues, and implement preventive measures to reduce risk, variability, and defects.</li><li>Promote and reinforce a culture of quality across the organization and the external partner network through communication, training, and example.</li><li>Build strong partnerships with external manufacturers and suppliers, driving accountability and continuous improvement across the manufacturing network.</li></ul>Essential Skills<ul><li>Bachelor's degree in Agriculture, Chemistry, Engineering, Biology, Pharmacy, or a related discipline.</li><li>8+ years of experience in Quality Assurance, Compliance, Manufacturing, or Supplier Quality within agriculture, biologicals, crop protection, biotechnology, or specialty chemicals.</li><li>Proven experience managing quality systems in outsourced or virtual manufacturing environments.</li><li>Demonstrated experience working with CMOs, toll manufacturers, formulators, and global supply partners.</li><li>Hands-on experience with supplier qualification, audits, quality agreements, CAPA, change management, and product launch processes.</li><li>Strong understanding of quality assurance principles, industry compliance requirements, and process-oriented quality systems.</li><li>Experience creating, implementing, and maintaining standard operating procedures (SOPs), particularly for toll manufacturers and new CMOs.</li><li>Proficiency in CAPA and root cause analysis methodologies, with the ability to drive effective corrective and preventive actions.</li><li>Capability to apply structured risk assessment and mitigation techniques to quality and compliance risks.</li><li>Strong communication, influence, and relationship management skills, including the ability to influence without direct authority.</li><li>Ability to operate effectively in a fast-paced, resource-constrained startup environment with shifting priorities.</li><li>Demonstrated agility and execution focus, with a track record of driving continuous improvement and cross-functional collaboration.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree in a relevant scientific or engineering discipline is preferred.</li><li>Experience in agriculture, biologicals, crop protection, biotechnology, or specialty chemicals with exposure to active ingredients and manufacturing processes.</li><li>Familiarity with six sigma or other continuous improvement methodologies.</li><li>Experience working more with manufacturing sites than laboratory environments, including support for selection and qualification of toll manufacturers.</li><li>Ability to develop and refine SOPs and quality processes for new and existing CMOs and tolling partners.</li><li>Strong discipline and process orientation, with a focus on implementing, following, and continuously improving quality systems.</li><li>Demonstrated capability in technology transfer and product launch support, including coordination with cross-functional teams.</li><li>Proven ability to anticipate and mitigate quality risks before they impact customers or supply.</li><li>Track record of balancing compliance rigor with the flexibility and agility needed in a growing organization.</li><li>Experience promoting a culture of quality and accountability across internal teams and external partners.</li><li>Forward-thinking mindset with strong planning and strategic thinking abilities, including comfort with evolving priorities.</li></ul>Work EnvironmentThis role operates in a dynamic, fast-paced startup environment that relies heavily on external manufacturing partners across multiple regions. The position focuses more on collaboration with manufacturing sites and external CMOs and toll manufacturers than on laboratory-based work. Priorities may shift as the organization grows and plans for the near future, so the successful candidate will demonstrate flexibility, adaptability, and comfort with evolving job functions. The culture emphasizes strategic thinking, continuous improvement, and strong cross-functional collaboration, with an expectation of clear communication and constructive partnership with internal stakeholders and external suppliers.Job Type &amp; LocationThis is a Contract to Hire position based out of Santa Monica, CA.Pay and BenefitsThe pay range for this position is $57.60 - $63.00/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 remote position.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 &amp; Compliance Lead Job DescriptionThe Quality &amp; Compliance Lead establishes and maintains a robust, fit-for-purpose quality management system to support the development, launch, and commercialization of agricultural products manufactured through external partners. This role serves as the primary quality interface with contract manufacturers, tolling partners, formulators, packagers, and logistics providers, ensuring regulatory compliance, consistent product quality, and reliable supply. The position drives continuous improvement across the external manufacturing network while balancing compliance rigor with the agility required in a fast-paced, resource-constrained startup environment.Responsibilities<ul><li>Develop and maintain a comprehensive Quality Management System (QMS) tailored to a virtual and outsourced manufacturing environment.</li><li>Establish clear quality standards, specifications, and release requirements for products manufactured by contract manufacturing organizations (CMOs) and tolling partners.</li><li>Qualify, onboard, and periodically assess contract manufacturers, formulators, packagers, and critical suppliers to ensure they meet quality and compliance expectations.</li><li>Define, implement, and maintain supplier quality agreements, including performance expectations and roles and responsibilities.</li><li>Monitor manufacturing performance using key performance indicators, scorecards, and regular business reviews, and address gaps proactively.</li><li>Support technology transfer, scale-up, validation, and commercial launch activities for new and existing products.</li><li>Ensure products and manufacturing operations comply with applicable regulatory requirements, customer specifications, and internal company standards.</li><li>Maintain a state of audit readiness and coordinate supplier audits, qualification assessments, and compliance reviews.</li><li>Lead investigations related to deviations, customer complaints, out-of-specification results, and non-conformances, ensuring thorough root cause analysis.</li><li>Drive corrective and preventive actions (CAPA), verify the effectiveness of implemented actions, and embed lessons learned into procedures and practices.</li><li>Oversee change control processes to assess and manage impacts on product quality, regulatory compliance, and supply continuity.</li><li>Identify, assess, and mitigate quality and compliance risks across the external manufacturing network using structured risk assessment and mitigation approaches.</li><li>Partner with Regulatory, Product Development, Supply Chain, and Commercial teams to support successful product introductions and lifecycle management.</li><li>Establish quality requirements for new products and ensure manufacturing readiness and robust controls are in place prior to launch.</li><li>Participate in process optimization initiatives to improve product consistency, manufacturability, and cost competitiveness.</li><li>Support inventory disposition decisions and product release processes, ensuring timely and compliant supply to customers.</li><li>Develop and execute supplier improvement plans and collaborate with manufacturing partners to enhance quality, reliability, and service.</li><li>Analyze quality trends, identify systemic issues, and implement preventive measures to reduce risk, variability, and defects.</li><li>Promote and reinforce a culture of quality across the organization and the external partner network through communication, training, and example.</li><li>Build strong partnerships with external manufacturers and suppliers, driving accountability and continuous improvement across the manufacturing network.</li></ul>Essential Skills<ul><li>Bachelor's degree in Agriculture, Chemistry, Engineering, Biology, Pharmacy, or a related discipline.</li><li>8+ years of experience in Quality Assurance, Compliance, Manufacturing, or Supplier Quality within agriculture, biologicals, crop protection, biotechnology, or specialty chemicals.</li><li>Proven experience managing quality systems in outsourced or virtual manufacturing environments.</li><li>Demonstrated experience working with CMOs, toll manufacturers, formulators, and global supply partners.</li><li>Hands-on experience with supplier qualification, audits, quality agreements, CAPA, change management, and product launch processes.</li><li>Strong understanding of quality assurance principles, industry compliance requirements, and process-oriented quality systems.</li><li>Experience creating, implementing, and maintaining standard operating procedures (SOPs), particularly for toll manufacturers and new CMOs.</li><li>Proficiency in CAPA and root cause analysis methodologies, with the ability to drive effective corrective and preventive actions.</li><li>Capability to apply structured risk assessment and mitigation techniques to quality and compliance risks.</li><li>Strong communication, influence, and relationship management skills, including the ability to influence without direct authority.</li><li>Ability to operate effectively in a fast-paced, resource-constrained startup environment with shifting priorities.</li><li>Demonstrated agility and execution focus, with a track record of driving continuous improvement and cross-functional collaboration.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree in a relevant scientific or engineering discipline is preferred.</li><li>Experience in agriculture, biologicals, crop protection, biotechnology, or specialty chemicals with exposure to active ingredients and manufacturing processes.</li><li>Familiarity with six sigma or other continuous improvement methodologies.</li><li>Experience working more with manufacturing sites than laboratory environments, including support for selection and qualification of toll manufacturers.</li><li>Ability to develop and refine SOPs and quality processes for new and existing CMOs and tolling partners.</li><li>Strong discipline and process orientation, with a focus on implementing, following, and continuously improving quality systems.</li><li>Demonstrated capability in technology transfer and product launch support, including coordination with cross-functional teams.</li><li>Proven ability to anticipate and mitigate quality risks before they impact customers or supply.</li><li>Track record of balancing compliance rigor with the flexibility and agility needed in a growing organization.</li><li>Experience promoting a culture of quality and accountability across internal teams and external partners.</li><li>Forward-thinking mindset with strong planning and strategic thinking abilities, including comfort with evolving priorities.</li></ul>Work EnvironmentThis role operates in a dynamic, fast-paced startup environment that relies heavily on external manufacturing partners across multiple regions. The position focuses more on collaboration with manufacturing sites and external CMOs and toll manufacturers than on laboratory-based work. Priorities may shift as the organization grows and plans for the near future, so the successful candidate will demonstrate flexibility, adaptability, and comfort with evolving job functions. The culture emphasizes strategic thinking, continuous improvement, and strong cross-functional collaboration, with an expectation of clear communication and constructive partnership with internal stakeholders and external suppliers.Job Type &amp; LocationThis is a Contract to Hire position based out of Santa Monica, CA.Pay and BenefitsThe pay range for this position is $57.60 - $63.00/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 remote position.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 &amp; Compliance Specialist - 100% REMOTE OPPORTUNITY Build the quality systems that enable the next generation of agricultural innovation! Join a fast-growing startup where you'll lead supplier quality, compliance, and continuous improvement across a global manufacturing network.Job DescriptionThe Quality &amp; Compliance Specialist establishes and maintains a robust, fit-for-purpose quality management system to support the development, launch, and commercialization of agricultural products manufactured through external partners. This role serves as the primary quality interface with contract manufacturers, tolling partners, formulators, packagers, and logistics providers, ensuring regulatory compliance, consistent product quality, and reliable supply. The position drives continuous improvement across the external manufacturing network while balancing compliance rigor with the agility required in a fast-paced, resource-constrained startup environment.Responsibilities<ul><li>Develop and maintain a comprehensive Quality Management System (QMS) tailored to a virtual and outsourced manufacturing environment.</li><li>Establish clear quality standards, specifications, and release requirements for products manufactured by contract manufacturing organizations (CMOs) and tolling partners.</li><li>Qualify, onboard, and periodically assess contract manufacturers, formulators, packagers, and critical suppliers to ensure they meet quality and compliance expectations.</li><li>Define, implement, and maintain supplier quality agreements, including performance expectations and roles and responsibilities.</li><li>Monitor manufacturing performance using key performance indicators, scorecards, and regular business reviews, and address gaps proactively.</li><li>Support technology transfer, scale-up, validation, and commercial launch activities for new and existing products.</li><li>Ensure products and manufacturing operations comply with applicable regulatory requirements, customer specifications, and internal company standards.</li><li>Maintain a state of audit readiness and coordinate supplier audits, qualification assessments, and compliance reviews.</li><li>Lead investigations related to deviations, customer complaints, out-of-specification results, and non-conformances, ensuring thorough root cause analysis.</li><li>Drive corrective and preventive actions (CAPA), verify the effectiveness of implemented actions, and embed lessons learned into procedures and practices.</li><li>Oversee change control processes to assess and manage impacts on product quality, regulatory compliance, and supply continuity.</li><li>Identify, assess, and mitigate quality and compliance risks across the external manufacturing network using structured risk assessment and mitigation approaches.</li><li>Partner with Regulatory, Product Development, Supply Chain, and Commercial teams to support successful product introductions and lifecycle management.</li><li>Establish quality requirements for new products and ensure manufacturing readiness and robust controls are in place prior to launch.</li><li>Participate in process optimization initiatives to improve product consistency, manufacturability, and cost competitiveness.</li><li>Support inventory disposition decisions and product release processes, ensuring timely and compliant supply to customers.</li><li>Develop and execute supplier improvement plans and collaborate with manufacturing partners to enhance quality, reliability, and service.</li><li>Analyze quality trends, identify systemic issues, and implement preventive measures to reduce risk, variability, and defects.</li><li>Promote and reinforce a culture of quality across the organization and the external partner network through communication, training, and example.</li><li>Build strong partnerships with external manufacturers and suppliers, driving accountability and continuous improvement across the manufacturing network.</li></ul>Essential Skills<ul><li>Bachelor's degree in Agriculture, Chemistry, Engineering, Biology, Pharmacy, or a related discipline.</li><li>8+ years of experience in Quality Assurance, Compliance, Manufacturing, or Supplier Quality within agriculture, biologicals, crop protection, biotechnology, or specialty chemicals.</li><li>Proven experience managing quality systems in outsourced or virtual manufacturing environments.</li><li>Demonstrated experience working with CMOs, toll manufacturers, formulators, and global supply partners.</li><li>Hands-on experience with supplier qualification, audits, quality agreements, CAPA, change management, and product launch processes.</li><li>Strong understanding of quality assurance principles, industry compliance requirements, and process-oriented quality systems.</li><li>Experience creating, implementing, and maintaining standard operating procedures (SOPs), particularly for toll manufacturers and new CMOs.</li><li>Proficiency in CAPA and root cause analysis methodologies, with the ability to drive effective corrective and preventive actions.</li><li>Capability to apply structured risk assessment and mitigation techniques to quality and compliance risks.</li><li>Strong communication, influence, and relationship management skills, including the ability to influence without direct authority.</li><li>Ability to operate effectively in a fast-paced, resource-constrained startup environment with shifting priorities.</li><li>Demonstrated agility and execution focus, with a track record of driving continuous improvement and cross-functional collaboration.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree in a relevant scientific or engineering discipline is preferred.</li><li>Experience in agriculture, biologicals, crop protection, biotechnology, or specialty chemicals with exposure to active ingredients and manufacturing processes.</li><li>Familiarity with six sigma or other continuous improvement methodologies.</li><li>Experience working more with manufacturing sites than laboratory environments, including support for selection and qualification of toll manufacturers.</li><li>Ability to develop and refine SOPs and quality processes for new and existing CMOs and tolling partners.</li><li>Strong discipline and process orientation, with a focus on implementing, following, and continuously improving quality systems.</li><li>Demonstrated capability in technology transfer and product launch support, including coordination with cross-functional teams.</li><li>Proven ability to anticipate and mitigate quality risks before they impact customers or supply.</li><li>Track record of balancing compliance rigor with the flexibility and agility needed in a growing organization.</li><li>Experience promoting a culture of quality and accountability across internal teams and external partners.</li><li>Forward-thinking mindset with strong planning and strategic thinking abilities, including comfort with evolving priorities.</li></ul>Work EnvironmentThis role operates in a dynamic, fast-paced startup environment that relies heavily on external manufacturing partners across multiple regions. The position focuses more on collaboration with manufacturing sites and external CMOs and toll manufacturers than on laboratory-based work. Priorities may shift as the organization grows and plans for the near future, so the successful candidate will demonstrate flexibility, adaptability, and comfort with evolving job functions. The culture emphasizes strategic thinking, continuous improvement, and strong cross-functional collaboration, with an expectation of clear communication and constructive partnership with internal stakeholders and external suppliers.Job Type &amp; LocationThis is a Contract to Hire position based out of Dallas, TX.Pay and BenefitsThe pay range for this position is $57.60 - $63.00/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 remote position.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 & Compliance Specialist - 100% REMOTE

Job Title: Quality Analyst – Inventory &amp;amp; Materials ControlJob DescriptionThe Quality Analyst – Inventory &amp;amp; Materials Control ensures the accuracy, quality, and traceability of materials issued from the warehouse to the manufacturing floor in a high-volume production environment. This role focuses on validating work order material requests, monitoring replenishment triggers, and confirming that materials are correctly backfilled to work centers. The position is part of a critical process improvement initiative and offers strong potential to grow into a long-term opportunity as the organization continues to enhance inventory hygiene and scalable manufacturing processes.Responsibilities<ul><li>Validate work order material requests to ensure accuracy, completeness, and alignment with production requirements.</li><li>Monitor replenishment triggers and ensure timely movement of materials from the warehouse to the manufacturing floor.</li><li>Confirm that all materials are correctly backfilled to work centers, maintaining accurate traceability for each work order.</li><li>Track materials using bills of materials (BOMs), including part numbers, serial numbers, and lot numbers, to support full traceability.</li><li>Work hands-on within a production or warehouse setting to verify material counts, locations, and movements.</li><li>Use ERP and/or warehouse management systems (WMS) to review, update, and reconcile work orders and inventory records.</li><li>Support inventory analysis activities to identify discrepancies, improve accuracy, and enhance overall inventory hygiene.</li><li>Apply high attention to detail and compliance-focused practices to ensure adherence to quality and logistics standards, including AS9100 guidelines where applicable.</li><li>Collaborate closely with production, materials, and logistics teams to ensure that materials availability supports production schedules.</li><li>Contribute to continuous improvement efforts aimed at developing scalable, repeatable manufacturing and materials control processes.</li><li>Assist with or perform data analysis on large material datasets, using advanced Excel tools such as pivot tables, when needed to support better auditing and decision-making.</li><li>Maintain clear documentation of materials movements, work order changes, and inventory adjustments to support audits and traceability requirements.</li></ul>Essential Skills<ul><li>3–5+ years of relevant experience in logistics, materials management, inventory control, or a closely related field</li><li>Hands-on experience working in a manufacturing environment, production floor, or warehouse setting.</li><li>Strong proficiency with work order processes and documentation in a manufacturing context.</li><li>Experience tracking materials using bills of materials (BOMs), including part numbers, serial numbers, and lot numbers.</li><li>Hands-on experience with ERP systems and/or warehouse management systems (WMS).</li><li>High attention to detail and accuracy in all materials, logistics, and compliance activities.</li><li>Background in logistics or materials management.</li><li>Inventory analysis experience, including identifying and resolving discrepancies.</li><li>Ability to work with limited direct oversight and operate independently while maintaining high standards.</li><li>Manufacturing experience strongly preferred, ideally within industries such as automotive, light medical manufacturing, or aerospace and defense.</li></ul>Additional Skills &amp;amp; Qualifications<ul><li>Bachelor’s degree preferred in Supply Chain, Business, Accounting, Engineering, or a related field.</li><li>Open to candidates with 7+ years of relevant experience without a degree.</li><li>Advanced Excel skills, including pivot tables and analysis of large material datasets, are a strong plus and indicate strong analytical aptitude.</li><li>AS9100 experience preferred but not required.</li><li>Exposure to automotive, light medical, or aerospace and defense manufacturing environments.</li><li>Interest in working within a mission-oriented organization focused on scalable autonomous equipment and modern defense technology.</li><li>Comfort working in a fast-paced, high-volume manufacturing setting with evolving processes and continuous improvement initiatives.</li></ul>Work EnvironmentThis role is based primarily on the warehouse and manufacturing floor, with approximately 90% of the time spent in a hands-on production environment. The position does not require travel. The shift is Monday through Friday from 3:30pm to 11:30pm. The role is closely tied to materials and production operations, and production teams work mandatory Saturdays every other Saturday, although overtime for this position is available but not mandatory. The environment emphasizes modern, scalable manufacturing processes and the use of ERP and warehouse management systems, as well as strong compliance practices aligned with standards such as AS9100. The organization offers a mission-driven culture focused on supporting critical defense technology through scalable autonomous equipment. There is also a company-wide shutdown from December 23rd to January 1st and 20 holidays throughout the year. The culture values meaningful, challenging work where you understand your contributions, emphasizes staying until the job is done while rarely requiring overtime, and promotes ongoing growth and continuous improvement in manufacturing and materials processes.Job Type &amp; LocationThis is a Contract position based out of Atlanta, GA.Pay and BenefitsThe pay range for this position is $100000.00 - $115000.00/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 Atlanta,GA.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 Analyst

Job Title: Quality Compliance Specialist – Quality AssuranceJob DescriptionThe Quality Compliance Specialist supports quality assurance activities in alignment with FDA, European MDD/MDR, and ISO regulations. Working under supervision, this role focuses on nonconformance (NCR) processes, data analysis, internal and external audits, service order records, supplier files, and monitoring key process metrics. The position requires frequent use of established industry practices, techniques, and standards to help maintain and improve the quality management system.Responsibilities<ul><li>Participate in quality system activities and support internal and external audits in compliance with FDA, European MDD/MDR, and ISO regulations.</li><li>Coordinate audit-related activities, including preparing documents, tracking audit requests, taking notes, scheduling conference rooms, and setting up communication channels.</li><li>Interface with subject matter experts to clarify and respond to audit requests and ensure timely completion of audit actions.</li><li>Work cross-functionally with other teams to track and manage NCR, rework, and deviation activities from initiation through closure.</li><li>Assist with identification, segregation, investigation, and final disposition of affected product associated with NCRs, rework, and deviations.</li><li>Identify and help implement continuous improvement activities within the quality management system (QMS).</li><li>Maintain quality records in accordance with established procedures and regulatory requirements.</li><li>Initiate and maintain supplier files on the approved supplier list, ensuring documentation is complete, accurate, and current.</li><li>Gather and update supplier information as needed to ensure supplier files remain in compliance with internal supplier procedures.</li><li>Manage Service Order Requests (SOR), including maintaining accurate records of SOR activities.</li><li>Ensure NCR materials associated with SORs are managed to comply with 30-day post-receipt requirements.</li><li>Maintain complete records of all SOR repairs and the costs associated with those repairs.</li><li>Develop, implement, and maintain SOR data logs to support analysis and trending of service-related activities.</li><li>Compile data and prepare presentations for periodic reviews of quality systems such as SORs and cost per SOR.</li><li>Collaborate with cross-functional teams to compile and generate periodic quality reports in a timely manner.</li><li>Work with cross-functional teams to track and ensure quality objectives established during management reviews are met.</li><li>Support organizational goals, objectives, policies, procedures, QSR, and applicable FDA regulations through daily work activities.</li><li>Perform other quality-related duties as assigned to support the overall effectiveness of the quality management system.</li></ul>Essential Skills<ul><li>Bachelor’s degree and a minimum of 2 years of related experience in the medical device industry.</li><li>Experience working within FDA and ISO-regulated environments, including familiarity with audits, NCR processes, and CAPA activities.</li><li>Ability to compile and analyze data, interpret trends, and present information clearly to stakeholders.</li><li>Competent document writing skills with strong attention to detail and accuracy.</li><li>Excellent written and verbal communication skills for effective interaction with cross-functional teams and subject matter experts.</li><li>Basic knowledge of current Good Manufacturing Practices (cGMP), FDA 21 CFR 820 Quality System Regulation (QSR), and ISO or other quality systems.</li><li>Ability to understand and follow QMS procedures, including standard operating procedures (SOPs) and test methods.</li><li>Proficiency with computer-based applications such as MS Word and MS Excel, and the ability to work with other office productivity tools.</li><li>Strong time management skills and the ability to prioritize and multi-task in a fast-paced environment.</li><li>Ability to operate effectively both as part of a team and independently, while demonstrating flexibility to changing requirements.</li><li>Hands-on experience in quality assurance, quality control, or compliance within the medical device sector.</li><li>Working knowledge of NCR and quality system processes, including data entry and documentation in quality systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with FDA and ISO audits, including preparation, coordination, and follow-up, is a plus.</li><li>Practical experience with NCR, CAPA, and deviation management is highly desirable.</li><li>Expereince in regulatory compliance and quality systems such as GMP and QMS is beneficial.</li><li>Experience with compiling quality metrics for trending and preparing presentations for management or quality reviews.</li><li>Familiarity with quality assurance methodologies, audit practices, and supplier quality controls.</li><li>Exposure to service order management, repair tracking, and cost analysis related to service activities.</li><li>Ability to collaborate with engineering, operations, and other cross-functional partners in a regulated environment.</li><li>Strong analytical mindset and problem-solving skills to support continuous improvement initiatives.</li><li>Interest in contributing to innovative cardiovascular medical technologies and advancing standards of care.</li></ul>Work EnvironmentThis role operates in a collaborative, office-based environment within a regulated medical device setting. You will work closely with an immediate team of approximately two colleagues and regularly interact cross-functionally with an additional two to three team members from other departments. The work involves frequent use of computer-based applications such as MS Word and MS Excel, preparation of documentation for audits, and maintenance of electronic records and data logs. The environment is fast-paced and dynamic, requiring flexibility, strong time management, and clear communication. The culture emphasizes innovation in cardiovascular therapy, adherence to FDA, MDD/MDR, and ISO quality standards, and continuous improvement of quality systems. Standard professional office attire is expected, with most activities performed in a typical office and meeting room setting.Job Type &amp; LocationThis is a Contract to Hire position based out of Santa Clara, CA.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 Santa Clara,CA.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 Assurance

Job Title: Quality Assurance ManagerFor immediate consideration you can apply using this link: https://talentassistant.actalentservices.com/assistant/bookings/85Y6bmzc﻿Job DescriptionThe Quality Assurance Manager leads all site-level quality and food safety operations at a Massachusetts manufacturing facility that produces annatto-derived ingredients through distillation. This role serves as the site authority on quality systems and regulatory compliance, oversees the implementation and maintenance of the Food Safety Plan, and ensures adherence to applicable FDA regulations (21 CFR 111 and 117). The Quality Assurance Manager manages the site Quality Management System (QMS) and holds quality responsibilities for both warehouse and production activities, acting as the primary quality leader for the entire facility.Responsibilities<ul><li>Lead all site-level quality assurance and food safety operations for a manufacturing facility producing annatto-derived ingredients through distillation.</li><li>Serve as the site authority on quality systems and regulatory compliance, ensuring alignment with internal policies and external regulatory requirements.</li><li>Oversee the implementation, maintenance, and continuous improvement of the Food Safety Plan in compliance with FDA regulations, including 21 CFR 111 and 21 CFR 117.</li><li>Manage and maintain the site Quality Management System (QMS), ensuring effective document control, standard operating procedures (SOPs), and quality records.</li><li>Ensure compliance with Good Manufacturing Practices (GMP) and applicable regulatory standards across production and warehouse operations.</li><li>Oversee quality responsibilities for warehouse and production activities, including inspection, in-process checks, and final product quality verification.</li><li>Direct and review batch records and production records to support accurate product release and traceability.</li><li>Lead and coordinate internal and external quality audits, including preparation, execution, response, and follow-up on corrective and preventive actions (CAPA).</li><li>Implement, monitor, and improve CAPA processes to address nonconformances and drive sustainable quality improvements.</li><li>Oversee laboratory-related quality activities, including testing, data review, and verification of food quality and safety parameters.</li><li>Ensure effective food safety and HACCP-related practices are implemented, monitored, and documented throughout manufacturing and warehousing operations.</li><li>Collaborate closely with production and warehouse teams to support compliant and efficient food manufacturing processes.</li><li>Monitor and verify compliance with regulatory requirements, customer specifications, and internal quality standards for all products.</li><li>Perform and oversee quality checks, inspections, and data entry related to quality metrics, ensuring accuracy and completeness of records.</li><li>Provide leadership, training, and guidance to staff on quality, food safety, GMP, and regulatory expectations.</li><li>Communicate clearly and effectively with cross-functional teams to resolve quality issues and support continuous improvement initiatives.</li><li>Use analytical, problem-solving, and decision-making skills to investigate quality deviations and implement effective solutions.</li><li>Utilize Microsoft Office and project management tools to manage documentation, reporting, and quality-related projects.</li><li>Act as the primary quality leader for the facility, overseeing the entire site’s quality and food safety performance.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Food Science, Chemistry, Biology, or a related technical field.</li><li>Advanced degree in a relevant technical discipline preferred.</li><li>Minimum 5–10 years of progressive quality assurance experience in food, dietary supplements, or ingredient manufacturing.</li><li>Deep working knowledge of FDA regulation 21 CFR 117 and familiarity with 21 CFR 111.</li><li>Proven experience with quality assurance in a manufacturing environment, including product release and production records review.</li><li>PCQI (Preventive Controls Qualified Individual) certification with demonstrated experience in overseeing food safety and product release.</li><li>Strong understanding of quality assurance, quality control, and quality management principles in food or ingredient manufacturing.</li><li>Hands-on experience with food safety programs, including HACCP and GMP implementation.</li><li>Experience with SOP development and management, CAPA processes, audits, batch record review, and document control.</li><li>Knowledge of laboratory practices related to food science, chemistry, and biology as they pertain to quality and food safety.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, PowerPoint, and Access.</li><li>Excellent analytical, problem-solving, and decision-making skills applied in a quality and regulatory context.</li><li>Strong communication skills, both written and verbal, with the ability to document clearly and present information effectively.</li><li>Demonstrated leadership skills with the ability to guide, influence, and support cross-functional teams.</li><li>Experience in food manufacturing, food quality, and food safety compliance within a regulated environment.</li><li>Familiarity with regulatory compliance requirements for food, dietary supplements, or ingredient manufacturing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in the food and beverage industry, particularly in food manufacturing or ingredient production, is strongly preferred.</li><li>Experience in annatto-derived ingredients, distillation processes, or similar ingredient manufacturing environments is beneficial.</li><li>Experience with quality checks, inspections, and data entry in a production or laboratory setting.</li><li>Exposure to regulatory compliance activities, including FDA inspections or third-party audits.</li><li>Experience with project management tools to support quality and continuous improvement projects.</li><li>Ability to manage multiple priorities and deadlines in a fast-paced manufacturing environment.</li><li>Strong organizational skills with attention to detail in documentation and record-keeping.</li><li>Comfort working closely with production, warehouse, and laboratory teams to support operational excellence.</li><li>Commitment to continuous improvement in quality systems, food safety, and regulatory compliance.</li></ul>Work EnvironmentThis is an on-site role based at a Massachusetts manufacturing facility that produces annatto-derived ingredients through distillation. The standard schedule is Monday through Friday from 8:30 a.m. to 4:30 p.m. The work environment includes close collaboration with production, warehouse, and laboratory areas, where adherence to Good Manufacturing Practices and food safety protocols is essential. The role involves working with quality systems, documentation, and regulatory records, as well as spending time on the production floor and in storage areas to oversee inspections, quality checks, and compliance activities. Appropriate professional and safety attire, including any required personal protective equipment, is expected in production and laboratory areas to maintain a safe and compliant facility.Job Type &amp; LocationThis is a Permanent position based out of Hadley, MA.Pay and BenefitsThe pay range for this position is $110000.00 - $140000.00/yr.PTO, Holiday, Summer HoursWorkplace TypeThis is a fully onsite position in Hadley,MA.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 Compliance Specialist II– Medical DeviceJob DescriptionThe Quality Compliance Specialist supports quality assurance activities in alignment with FDA, European MDD/MDR, and ISO regulations. Working under supervision, this role focuses on nonconformance (NCR) processes, data analysis, internal and external audits, service order records, supplier files, and monitoring key process metrics. The position requires frequent use of established industry practices, techniques, and standards to help maintain and improve the quality management system.Responsibilities<ul><li>Participate in quality system activities and support internal and external audits in compliance with FDA, European MDD/MDR, and ISO regulations.</li><li>Coordinate audit-related activities, including preparing documents, tracking audit requests, taking notes, scheduling conference rooms, and setting up communication channels.</li><li>Interface with subject matter experts to clarify and respond to audit requests and ensure timely completion of audit actions.</li><li>Work cross-functionally with other teams to track and manage NCR, rework, and deviation activities from initiation through closure.</li><li>Assist with identification, segregation, investigation, and final disposition of affected product associated with NCRs, rework, and deviations.</li><li>Identify and help implement continuous improvement activities within the quality management system (QMS).</li><li>Maintain quality records in accordance with established procedures and regulatory requirements.</li><li>Initiate and maintain supplier files on the approved supplier list, ensuring documentation is complete, accurate, and current.</li><li>Gather and update supplier information as needed to ensure supplier files remain in compliance with internal supplier procedures.</li><li>Manage Service Order Requests (SOR), including maintaining accurate records of SOR activities.</li><li>Ensure NCR materials associated with SORs are managed to comply with 30-day post-receipt requirements.</li><li>Maintain complete records of all SOR repairs and the costs associated with those repairs.</li><li>Develop, implement, and maintain SOR data logs to support analysis and trending of service-related activities.</li><li>Compile data and prepare presentations for periodic reviews of quality systems such as SORs and cost per SOR.</li><li>Collaborate with cross-functional teams to compile and generate periodic quality reports in a timely manner.</li><li>Work with cross-functional teams to track and ensure quality objectives established during management reviews are met.</li><li>Support organizational goals, objectives, policies, procedures, QSR, and applicable FDA regulations through daily work activities.</li><li>Perform other quality-related duties as assigned to support the overall effectiveness of the quality management system.</li></ul>Essential Skills<ul><li>Bachelor’s degree and a minimum of 2 years of related experience in the medical device industry.</li><li>Experience working within FDA and ISO-regulated environments, including familiarity with audits, NCR processes, and CAPA activities.</li><li>Ability to compile and analyze data, interpret trends, and present information clearly to stakeholders.</li><li>Competent document writing skills with strong attention to detail and accuracy.</li><li>Excellent written and verbal communication skills for effective interaction with cross-functional teams and subject matter experts.</li><li>Basic knowledge of current Good Manufacturing Practices (cGMP), FDA 21 CFR 820 Quality System Regulation (QSR), and ISO or other quality systems.</li><li>Ability to understand and follow QMS procedures, including standard operating procedures (SOPs) and test methods.</li><li>Proficiency with computer-based applications such as MS Word and MS Excel, and the ability to work with other office productivity tools.</li><li>Strong time management skills and the ability to prioritize and multi-task in a fast-paced environment.</li><li>Ability to operate effectively both as part of a team and independently, while demonstrating flexibility to changing requirements.</li><li>Hands-on experience in quality assurance, quality control, or compliance within the medical device sector.</li><li>Working knowledge of NCR and quality system processes, including data entry and documentation in quality systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with FDA and ISO audits, including preparation, coordination, and follow-up, is a plus.</li><li>Practical experience with NCR, CAPA, and deviation management is highly desirable.</li><li>Experience in regulatory compliance and quality systems such as GMP and QMS is beneficial.</li><li>Experience with compiling quality metrics for trending and preparing presentations for management or quality reviews.</li><li>Familiarity with quality assurance methodologies, audit practices, and supplier quality controls.</li><li>Exposure to service order management, repair tracking, and cost analysis related to service activities.</li><li>Ability to collaborate with engineering, operations, and other cross-functional partners in a regulated environment.</li><li>Strong analytical mindset and problem-solving skills to support continuous improvement initiatives.</li><li>Interest in contributing to innovative cardiovascular medical technologies and advancing standards of care.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Santa Clara, CA.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 Santa Clara,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 Assurance AssociateJob DescriptionThe Quality Assurance Associate supports a robust quality system by managing product complaints, conducting investigations, and ensuring compliance with applicable regulations and internal procedures. This role independently handles customer inquiries, performs detailed complaint evaluations, supports regulatory reporting, and contributes to process improvements that enhance product quality and customer satisfaction.Responsibilities<ul><li>Independently field inquiries received by phone, electronic, or verbal correspondence and determine whether they qualify as complaints in accordance with applicable standard operating procedures.</li><li>Document reported issues accurately and completely, following all relevant SOPs and quality system requirements.</li><li>Provide technical support and remote troubleshooting guidance to users and customers as needed.</li><li>Review associated records independently and contact users and customers to collect detailed information on treatments, product performance, and functionality.</li><li>Conduct periodic follow-up with customers and internal stakeholders to ensure timely closure of complaints.</li><li>Manage customer relationships and expectations throughout the complaint investigation process, maintaining clear and professional communication.</li><li>Independently complete complaint investigations, including coordinating or executing product returns and subsequent evaluations as required.</li><li>Review manufacturing records and other relevant documentation as part of complaint investigations, ensuring proper approvals are obtained prior to closure.</li><li>Develop practical solutions to a variety of moderately complex problems related to product quality and performance.</li><li>Conduct statistical analysis of complaint trends and provide insights that support quality improvement initiatives.</li><li>Support the training program by training users on the complaint process, tools, and methods used to assess and investigate complaints.</li><li>Support and, when appropriate, identify operational changes to improve efficiencies in all aspects of complaint handling.</li><li>Sometimes lead investigations associated with product deviations, product non-conformances, corrective and preventive actions (CAPAs), scrap, and rework, and analyze data to identify root causes and opportunities for quality improvement.</li><li>Update internal operating procedures and specifications through the document change process to reflect process improvements and regulatory requirements.</li><li>Support and participate in internal quality system audits by providing documentation, explanations, and follow-up actions.</li><li>Support external quality system audits by assisting with preparation, participating in audit activities, and implementing corrective actions as needed.</li><li>Evaluate complaints to determine whether submission of a Medical Device Report (MDR) or other Vigilance Report is required based on regulatory criteria.</li><li>Prepare and submit MDRs and Vigilance Reports within required regulatory timelines, ensuring accuracy and completeness of information.</li></ul>Essential Skills<ul><li>Experience in quality assurance or other regulated industry or similar experience (preferred).</li><li>Knowledge of quality principles and practices, including inspection activities (inspect*).</li><li>Familiarity with FDA regulations and expectations for regulated products.</li><li>Understanding of Good Manufacturing Practices (GMP).</li><li>Understanding of Good Laboratory Practices (GLP).</li><li>Experience or exposure to medical device (Med* Device) quality or regulatory environments.</li><li>Strong technical writing skills, with the ability to document investigations, complaints, and reports clearly and accurately (required).</li><li>Strong general problem-solving skills and the ability to develop solutions to moderately complex issues (required).</li><li>Ability to manage multiple priorities and work effectively despite interruptions (required).</li><li>Customer service skills, including the ability to manage customer expectations and maintain professional communication.</li><li>Proficiency with Microsoft Excel for tracking, trending, and statistical analysis of complaint data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor of Science (BS) in a Physical Science or Engineering, or equivalent experience (required).</li><li>Experience working within a quality system in a regulated industry, such as medical devices, pharmaceuticals, or related fields (preferred).</li><li>Experience supporting or participating in internal and external quality system audits.</li><li>Experience with complaint handling processes, including documentation, investigation, and closure.</li><li>Familiarity with Medical Device Reporting (MDR) and Vigilance reporting requirements and timelines.</li><li>Ability to adapt to constant and sometimes sudden changes in role, processes, or organizational priorities.</li><li>Strong interpersonal and communication skills for collaborating with cross-functional teams and training users on complaint processes.</li><li>Attention to detail and accuracy in documentation, data analysis, and regulatory reporting.</li></ul>Work EnvironmentThis is a first-shift position with core hours of 7:00 a.m. to 3:30 p.m., Monday through Friday, with an additional hour of work per day expected. There may be occasions when work of up to four hours on Saturdays is requested; while this is typically voluntary, candidates should be comfortable and capable of working Saturdays as required. The work environment supports a family-oriented culture where team members actively support one another and collaborate to achieve shared goals. The organization regularly undergoes change, so the ideal candidate is comfortable working in a dynamic environment where responsibilities and processes may evolve. The role operates within a regulated quality system environment, using standard office and computer-based tools such as Microsoft Excel, and involves frequent communication by phone and electronic correspondence with customers and internal teams.Job Type &amp; LocationThis is a Contract position based out of Sturtevant, WI.Pay and BenefitsThe pay range for this position is $24.00 - $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 Sturtevant,WI.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 Assurance Associate

Job Title: Part Time Quality Assurance SpecialistJob DescriptionThe Quality Assurance Specialist provides quality oversight for manufacturing operations within an ISO-regulated IVD manufacturing environment. This role focuses on detailed review of batch records and manufacturing documentation to ensure accuracy, completeness, and regulatory compliance prior to product release. The specialist supports lot release activities, maintains quality system records, and contributes to investigations and audits that uphold high standards of quality and regulatory compliance.Responsibilities<ul><li>Review manufacturing batch records and associated documentation to ensure accuracy, completeness, and compliance prior to product release.</li><li>Examine raw material inspection records and verify that materials meet established specifications and quality requirements.</li><li>Review equipment calibration documentation to confirm that instruments and equipment are properly calibrated and suitable for use in manufacturing.</li><li>Support lot release activities by verifying that all required quality checks and documentation are complete and compliant.</li><li>Prepare Certificates of Analysis as needed to support product release and customer or regulatory requirements.</li><li>Review and approve quality system records including nonconformance reports (NCRs), corrective and preventive actions (CAPAs), complaints, deviations, and change orders.</li><li>Support and participate in investigations of quality events by identifying discrepancies, gathering relevant data, and contributing to root cause analyses.</li><li>Perform risk assessments related to quality events and verify the effectiveness of implemented corrective and preventive actions.</li><li>Maintain accurate and organized quality records in accordance with ISO standards and regulatory requirements.</li><li>Support internal and external audits by providing documentation, answering quality-related questions, and demonstrating compliance with applicable standards and regulations.</li><li>Participate in training activities to maintain current knowledge of quality procedures, regulatory requirements, and best practices.</li><li>Assist with various quality projects and initiatives as business needs arise, contributing to continuous improvement of quality systems and processes.</li><li>Help maintain compliance with ISO standards and support quality system activities within a regulated IVD/CDMO environment.</li><li>Apply knowledge of 21 CFR 820 regulations to daily quality assurance activities and decisions.</li><li>Collaborate with Operations, Manufacturing, Quality, and leadership teams to ensure alignment on quality expectations and decisions.</li><li>Communicate quality findings and recommendations clearly to both technical and non-technical stakeholders.</li><li>Contribute to document control activities to ensure that procedures, work instructions, and records are current, controlled, and properly implemented.</li></ul>Essential Skills<ul><li>At least 3 years of quality assurance experience in regulated manufacturing environments.</li><li>Bachelor's degree in Life Sciences, Engineering, Business, or a related field.</li><li>Demonstrated experience with ISO-regulated quality systems, including maintaining compliance with ISO standards.</li><li>Working knowledge of 21 CFR 820 regulations and their application in an IVD or CDMO setting.</li><li>Strong batch record review skills, with the ability to identify errors, discrepancies, and gaps in documentation.</li><li>Hands-on experience reviewing and managing NCRs, CAPAs, complaints, deviations, and other quality events.</li><li>Understanding of GMP, FDA expectations, and regulatory compliance in a manufacturing context.</li><li>Proficiency in quality assurance and quality control principles, including risk assessment and effectiveness checks.</li><li>Strong document control skills, including managing and reviewing controlled procedures and records.</li><li>Ability to interpret regulatory requirements and quality standards and apply them to practical manufacturing and quality decisions.</li><li>Independent problem-solving and decision-making capabilities in a regulated environment.</li><li>Strong communication skills with both technical and non-technical stakeholders.</li><li>Proficiency with computer systems and reporting tools used for quality documentation and data analysis.</li></ul>Additional Skills &amp; Qualifications<ul><li>Preferred knowledge of IVDR and its application to IVD products.</li><li>Experience working in an IVD or CDMO environment supporting genomics, molecular diagnostics, or biotechnology products.</li><li>Familiarity with ISO 13485 or similar ISO standards applicable to medical devices and diagnostics.</li><li>Experience supporting internal and external audits, including preparation of documentation and responses to findings.</li><li>Expirience in conducting or supporting root cause analyses and continuous improvement projects.</li><li>Ability to collaborate effectively with cross-functional teams in Operations, Manufacturing, Quality, and leadership.</li><li>Comfort working in a high-visibility quality role with direct influence on product release and regulatory compliance.</li></ul>Work EnvironmentThis position is onsite and offers a flexible part-time schedule of approximately 20–30 hours per week. The role is based in a regulated IVD/CDMO manufacturing environment that supports cutting-edge genomics, molecular diagnostics, and biotechnology products. You will work closely with Operations, Manufacturing, Quality, and leadership teams in a rapidly growing organization. The environment emphasizes collaboration, regulatory compliance, and continuous improvement, with diverse responsibilities spanning batch review, quality systems, investigations, audits, and change control.Job Type &amp; LocationThis is a Contract position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $30.00 - $37.00/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 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.

Lead Food Safety. Drive Quality. Make an Impact.Are you passionate about food safety and quality excellence? Do you thrive in a fast-paced manufacturing environment where your expertise directly impacts product integrity and consumer trust? We are seeking a Quality Assurance Lead to help champion our food safety culture, support our growing operations, and lead a team dedicated to delivering high-quality products every day.This is an exciting opportunity for a quality professional who enjoys being hands-on on the production floor, mentoring team members, and partnering across departments to continuously improve food safety and quality systems.<hr><h2>About the Role</h2>As the Quality Assurance Lead, you will play a key leadership role in ensuring our products consistently meet regulatory requirements, customer expectations, and internal quality standards. You will oversee quality monitoring activities, environmental and allergen testing programs, equipment calibrations, and documentation processes while providing guidance and support to QA Technicians.Success in this role requires strong technical knowledge, sound decision-making abilities, and a commitment to creating a culture of accountability, transparency, and continuous improvement.<hr><h2>What You'll Do</h2><h3>Food Safety &amp; Quality Oversight</h3><ul><li>Lead quality assurance activities on the production floor to ensure compliance with food safety regulations and company standards.</li><li>Monitor production processes and verify adherence to product specifications, quality requirements, and food safety protocols.</li><li>Perform daily calibrations of scales, thermometers, and other quality-related equipment to ensure accurate measurements.</li><li>Investigate and resolve quality deviations, equipment issues, and out-of-specification findings.</li><li>Escalate critical food safety concerns, including Critical Control Point (CCP) deviations, for immediate corrective action.</li></ul><h3>Testing &amp; Verification</h3><ul><li>Conduct and support environmental monitoring activities, including environmental swabbing programs.</li><li>Perform ATP verification and allergen testing while maintaining accurate documentation of results.</li><li>Troubleshoot issues identified during testing and implement corrective actions to reduce food safety risks.</li></ul><h3>Documentation &amp; Compliance</h3><ul><li>Maintain thorough and accurate quality records to support traceability, audits, and regulatory compliance.</li><li>Verify completion and accuracy of production records, line checks, inspection reports, and quality documentation.</li><li>Support internal audits, customer audits, and regulatory inspections.</li><li>Document product holds, quality incidents, and corrective actions in accordance with company procedures.</li></ul><h3>Leadership &amp; Team Development</h3><ul><li>Provide day-to-day leadership, coaching, and support to Quality Assurance Technicians.</li><li>Conduct onboarding, training, and retraining activities related to food safety and quality standards.</li><li>Identify development opportunities and help build technical capabilities across the QA team.</li><li>Make informed decisions regarding product disposition, inspections, and quality-related concerns.</li></ul><h3>Continuous Improvement</h3><ul><li>Partner with Production, Operations, and other departments to resolve quality issues and prevent recurrence.</li><li>Support initiatives that strengthen food safety programs, improve operational performance, and enhance product quality.</li><li>Contribute ideas and recommendations in an environment that values collaboration and innovation.</li></ul><hr><h2>What We're Looking For</h2><h3>Required Qualifications</h3><ul><li>2–3 years of Quality Assurance experience within food manufacturing.</li><li>3+ years of overall food manufacturing experience, ideally within bakery, pizza, or related food production environments.</li><li>1+ year of leadership or supervisory experience with demonstrated success leading teams.</li><li>Associate degree in Food Science, Microbiology, or a related field, or an equivalent combination of education and experience.</li><li>Strong knowledge of food safety regulations, quality systems, and audit requirements.</li><li>Understanding of HACCP principles and Preventive Controls for Human Food (PCQI) requirements.</li><li>Experience conducting calibrations, environmental monitoring, ATP testing, and allergen verification.</li><li>Excellent documentation, communication, and problem-solving skills.</li><li>Ability to confidently enforce food safety standards and make quality-related decisions in a fast-paced manufacturing environment.</li></ul><h3>Preferred Qualifications</h3><ul><li>Bakery or pizza manufacturing experience.</li><li>PCQI and/or HACCP certification.</li><li>Educational background or coursework in Chemistry, Food Science, Microbiology, or related disciplines.</li><li>Experience supporting audits, regulatory inspections, and continuous improvement initiatives.</li></ul><hr><h2>Why Join Us?</h2>Growth Opportunities – Advance your career in a growing organization that invests in employee development.Professional Certifications – Gain opportunities to earn valuable industry certifications such as PCQI and HACCP.Leadership Exposure – Work in a transparent, open-door culture where leadership is accessible and employee input is valued.Meaningful Impact – Play a critical role in protecting consumers and maintaining the highest food safety standards.Collaborative Environment – Be part of a team committed to quality, accountability, and continuous improvement.<hr><h2>Work Environment &amp; Schedule</h2><ul><li>Shift: Second Shift (Typically 2:00 PM – 10:30 PM)</li><li>Shift Differential: Available for second and third shifts</li><li>Work within a modern food manufacturing environment producing pizza and bakery products.</li><li>Split your time between the production floor and QA office areas conducting inspections, testing, documentation, and team support.</li><li>Join a collaborative quality team consisting of Quality Technicians, a Quality Supervisor, and the Quality Assurance Lead.</li></ul><hr><h3>Ready to Take the Lead in Quality Excellence?</h3>If you're a quality-focused leader who is passionate about food safety, team development, and continuous improvement, we'd love to hear from you. Apply today and help us deliver safe, high-quality products that customers can trust.Job Type &amp; LocationThis is a Contract to Hire position based out of Bourbonnais, IL.Pay and BenefitsThe pay range for this position is $23.00 - $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 Bourbonnais,IL.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 Assurance Lead

Job Title: Quality Assurance Manager Job DescriptionWe are seeking a Quality Assurance Manager with expertise in QA Lifecycle management to join our team. The successful candidate will partner with Regulatory, Manufacturing, QA, and QC liaisons to build dossier components and ensure compliance with company SOPs and health authority regulations. This role involves managing a team of QA specialists and overseeing various quality management and audit activities.Responsibilities<ul><li>Partner with Regulatory, Manufacturing, QA, and QC liaisons to build dossier components.</li><li>Work within the document change system and track progress of documentation.</li><li>Interact with responsible parties to ensure timely tracking and distribution of documents.</li><li>Independently complete daily activities in compliance with company SOPs and regulations.</li><li>Review documents to ensure data consistency and compliance with required formats.</li><li>Perform audits for the Quality Management System, including investigations, documentation, training, QC and MFG data, and vendor management.</li><li>Maintain the Training system and documentation.</li><li>Provide monthly metrics to Quality Management.</li><li>Ensure quality systems comply with regulatory requirements and meet AIM needs.</li><li>Collaborate with stakeholders to keep systems updated with regulatory trends and industry standards.</li><li>Manage a team of direct reports, overseeing their training, performance, and career development.</li><li>Lead and coordinate on-site audits by regulatory authorities, ensuring audit readiness and follow-ups.</li><li>Manage internal audit and supplier management programs.</li><li>Oversee the document management system according to internal procedures.</li><li>Review, assess, and approve change controls, non-conformances, and CAPAs.</li><li>Ensure product quality meets company and cGMP standards.</li><li>Perform gap analysis and propose plans to improve QMS performance.</li><li>Identify improvement opportunities for the QMS through quality metrics evaluation.</li><li>Oversee document storage according to company needs.</li><li>Meet regularly with the Director to update ongoing activities and address issues.</li><li>Ensure compliance with Health, Safety, and Environment protection rules.</li></ul>Essential Skills<ul><li>Bachelor's or Master's degree in Sciences.</li><li>Experience in the pharmaceutical industry, preferably with small to mid-sized companies.</li><li>Expertise in QA Lifecycle management.</li><li>Managerial experience overseeing 2-3 direct reports.</li><li>Proficiency in technical writing, data review, quality control, internal audit, and documentation review.</li><li>Knowledge of GMP and pharmaceutical standards.</li></ul>Additional Skills &amp; Qualifications<ul><li>Excellent written and verbal communication skills.</li><li>Effective time management and organizational skills.</li><li>Ability to establish and maintain effective working relationships.</li><li>Availability to travel and manage travel schedules.</li><li>Valid driver's license and proficient driving skills.</li><li>Ability to lift up to 50 pounds.</li><li>Awareness of research regulatory requirements, GDP, and ICH guidelines.</li><li>Proficiency with Microsoft Office Suite.</li><li>Knowledge of medical terminology.</li></ul>Work EnvironmentCandidates will work in a fast-paced manufacturing environment with a team-oriented culture. The position is onsite five days a week with standard hours from 8:30 AM to 5:00 PM. Flexibility for overtime is required, with occasional work outside standard hours. The dress code is business casual. Candidates should be comfortable handling physical files and lifting up to 20 pounds.Job Type &amp; LocationThis is a Contract to Hire position based out of New Brunswick, NJ.Pay and BenefitsThe pay range for this position is $61.00 - $72.00/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 New Brunswick,NJ.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 Assurance Manager

Job Title: Quality Assurance SpecialistJob DescriptionThe Quality Assurance Specialist maintains and continuously improves the site’s quality management system and food safety programs for food ingredient manufacturing facility that supplies ingredients to the food industry. This role functions as a junior Quality Assurance Manager in training, offering significant autonomy and exposure to quality systems, audits, and regulatory compliance, with a clear path toward a full Quality Assurance Manager position.Responsibilities<ul><li>Maintain, update, and improve the quality management system (QMS) and all related documentation across the facility.</li><li>Review, investigate, and document non-conformances, ensuring timely corrective actions and proper records of corrections and outcomes.</li><li>Manage change control requests and quality documentation to ensure all changes meet internal standards and regulatory requirements.</li><li>Maintain and improve the food safety program (PCQI), including cleaning and hygiene protocols, to ensure consistent product safety.</li><li>Maintain, update, and implement the HACCP plan and follow corrective and preventive action (CAPA) processes as needed.</li><li>Perform and lead internal and external audits, including FDA audits, FSSC audits, and other regulatory or certification audits.</li><li>Ensure ongoing compliance with regulatory requirements, including FDA, FSMA, and CFIA regulations.</li><li>Oversee product labeling for new products and regulatory changes, and ensure internal stakeholders receive timely updates on requirements.</li><li>Coordinate, deliver, and maintain food safety training for all personnel on site, ensuring training records remain current.</li><li>Handle audits, CAPA activities, root cause analyses (RCA), and non-conformance management for the entire site.</li><li>Maintain quality documentation and quality tracking systems to support continuous improvement and regulatory readiness.</li><li>Report monthly on findings, including corrective actions, resolutions, improvements, and root causes, and present these to relevant stakeholders.</li><li>Collaborate with production, laboratory, and other functional teams to ensure quality and food safety standards are consistently applied throughout the plant.</li></ul>Essential Skills<ul><li>Demonstrated experience in quality assurance within a food or food-ingredient manufacturing environment.</li><li>Hands-on knowledge of quality management systems (QMS) and their implementation in a plant setting.</li><li>Practical experience with HACCP (Hazard Analysis Critical Control Point) programs, including plan maintenance and execution.</li><li>Proficiency with PCQI (Preventive Controls Qualified Individual) responsibilities and food safety program management.</li><li>Working knowledge of FSMA (Food Safety Modernization Act) requirements and their application in manufacturing.</li><li>Familiarity with CFIA (Canadian Food Inspection Agency) regulations and expectations.</li><li>Experience with FSSC-based audits or similar food safety certification schemes.</li><li>Ability to manage and document CAPA processes, root cause analyses (RCA), and non-conformance investigations.</li><li>Strong documentation, reporting, and organizational skills to maintain complete and accurate quality records.</li><li>Ability to lead and participate in internal and external audits, including regulatory and certification audits.</li><li>Capability to coordinate and deliver food safety training across a site.</li><li>Comfort working with cross-functional teams in a manufacturing environment to uphold quality and food safety standards.</li></ul>Additional Skills &amp; Qualifications<ul><li>Background in Food Safety, Microbiology, Biology, or a related scientific discipline.</li><li>Formal training or certification in HACCP.</li><li>PCQI training or certification.</li><li>Familiarity with FDA, FSMA, CFIA, and FSSC frameworks and expectations.</li><li>Experience with quality assurance with ingredient production is beneficial.</li><li>Interest in growing into a full Quality Assurance Manager role and taking on broader leadership responsibilities over time.</li><li>Strong analytical and problem-solving skills, especially in investigating non-conformances and implementing sustainable improvements.</li><li>Effective communication skills to clearly convey quality and food safety requirements to diverse teams.</li></ul>Work EnvironmentThe Quality Assurance Specialist works closely with all departments in the facility and primarily operates from an office environment, with occasional visits to production areas and laboratories as needed for audits, investigations, and verification activities. The position follows a first-shift schedule, Monday through Friday, with a flexible start time to support work–life balance. The site is smaller in scale, which allows one person to manage the quality systems more effectively and gain broad exposure to all aspects of quality and food safety. The organization offers strong benefits, including comprehensive medical coverage, and emphasizes autonomy, professional growth, and promotion opportunities within quality assurance.Job Type &amp; LocationThis is a Permanent position based out of Glendale, WI.Pay and BenefitsThe pay range for this position is $70000.00 - $80000.00/yr.This company offers health insurance, dental insurance, and vision insurance. They also offer 401k match, paid vacation, and paid holidays. Their health insurance covers 100% of their medical so it is a very strong benefits program.Workplace TypeThis is a fully onsite position in Glendale,WI.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 Assurance Specialist

Description
					Provide quality oversight for manufacturing operations, ensuring compliance with cGMP regulations and internal procedures.
Review and disposition raw materials, plasmids, drug substance, and drug product batches.
Review and approve batch production records, testing records, and manufacturing documentation.
Support batch record review and release activities for materials and products.
Review, investigate, and document deviations, ensuring appropriate corrective and preventive actions are implemented.
Author, review, and revise SOPs, batch records, policies, and training materials.
Participate in real-time quality oversight activities within manufacturing operations and cleanroom environments.
Partner with cross-functional teams to support manufacturing readiness, startup activities, and continuous improvement initiatives.
Ensure adherence to data integrity principles and training requirements.
Monitor manufacturing operations for compliance with established specifications and procedures.
Support internal audits and regulatory inspection readiness activities.
Escalate quality, manufacturing, and safety concerns as appropriate.
Serve as a subject matter expert (SME) and mentor for new team members.
Lead and contribute to quality and compliance-related projects across multiple functional groups.
Drive root cause investigations and corrective actions for complex quality issues.
										Skills
					Quality assurance, drug substance, drug product, Batch record, raw materials, deviations, change control, environmental monitoring, microbioloigcal testing, Batch record review, Authoring SOPs, Sop, audit, compliance
										Top Skills Details
					Quality assurance,drug substance,drug product,Batch record,raw materials,deviations,change control,environmental monitoring,microbioloigcal testing,Batch record review
										Additional Skills &amp; Qualifications
					BS or equalivalent experience with in science industry within quality assurance
 2-5 Years experience 
Knowledge of FDA, EU, ICH guidelines, and relevant regulations.
Experience with quality systems, including batch record review, deviation management, and change control.
Proficiency in authoring and reviewing GMP documentation.
Familiarity with environmental monitoring and microbiological testing.
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Contract position based out of Norwood, MA.Pay and BenefitsThe pay range for this position is $42.00 - $52.00/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 Norwood,MA.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.

QA SpecialistJob DescriptionThe Quality Systems Specialist supports cGMP quality system activities within a biopharmaceutical manufacturing environment, executing and maintaining processes managed through the MasterControl electronic Quality Management System (eQMS). This role involves building and managing a supplier and vendor quality program, including qualification and auditing of suppliers, with occasional domestic and international travel required. The specialist is responsible for GMP training programs, validation and qualification document review, deviations, investigations, CAPAs, and change controls. Collaboration cross-functionally to ensure compliance with internal procedures and global regulatory requirements is essential.Responsibilities<ul><li>Build and manage a supplier and vendor quality program, including qualification and auditing of suppliers.</li><li>Execute and maintain processes managed through the MasterControl eQMS.</li><li>Conduct GMP training programs, validation and qualification document reviews.</li><li>Handle deviations, investigations, CAPAs, and change controls.</li><li>Collaborate cross-functionally to ensure compliance with internal procedures and global regulatory requirements.</li><li>Support continuous improvement initiatives.</li><li>Coordinate internal and external audits.</li><li>Manage training documentation and oversee change control governance.</li><li>Support Annual Product Review (APR) preparation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree or above in a Scientific discipline</li><li>1+ years of quality experience in the biopharma/pharmaceutical industry preferred</li><li>Experience in managing vendors and auditing</li></ul>Work EnvironmentThe position operates on a 1st shift schedule from Monday to Friday, starting between 7-9am for 8-hour workdays. This position operates in an office based environment.Job Type &amp; LocationThis is a Permanent position based out of Waunakee, WI.Pay and BenefitsThe pay range for this position is $62000.00 - $90000.00/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 Waunakee,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 Assurance Specialist (Contract)Job DescriptionThe Quality Assurance Specialist will support a state-of-the-art lentiviral vector development and manufacturing facility by overseeing quality documentation for externally manufactured products, managing incoming GMP material release and disposition, and contributing to broader QA activities. This role partners closely with Supply Chain, Manufacturing, and external vendors to ensure product quality, regulatory compliance, and continuous improvement in a dynamic cell and gene therapy environment.Responsibilities<ul><li>Perform detailed quality review of executed batch records, manufacturing records, and associated release documentation received from Contract Manufacturing Organizations (CMOs).</li><li>Review manufacturing deviations, investigations, change controls, corrective and preventive actions (CAPAs), and other quality events that impact external batch disposition.</li><li>Evaluate manufacturing and testing documentation to support final external batch release disposition decisions in alignment with cGMP and regulatory expectations.</li><li>Perform quality review and disposition of incoming GMP materials used in the GMP manufacturing facility, ensuring materials meet specifications and are appropriately controlled.</li><li>Support the Vendor Management program by participating in vendor oversight activities and helping ensure vendors meet quality and regulatory requirements, as needed.</li><li>Author, review, and approve Standard Operating Procedures (SOPs) and other controlled documents as a Quality Assurance representative, ensuring documentation is accurate, compliant, and current.</li><li>Collaborate cross-functionally with QA Operations, Supply Chain, Manufacturing, and vendors to resolve issues, support continuous improvement, and maintain alignment on quality standards.</li><li>Work with materials management documentation, including revisions related to out-of-specification (OOS) results, deviations, batch record review, and updates within the ERP system (NetSuite).</li><li>Participate in or support PQ (Performance Qualification) testing and related quality activities, as applicable.</li><li>Communicate effectively with vendors and suppliers, as needed, to clarify quality requirements, address documentation questions, and support timely batch disposition.</li><li>Contribute to the implementation and maintenance of quality management system elements, including risk management practices that support Phase 1 and first-in-human programs.</li><li>Demonstrate a continuous improvement mindset by identifying opportunities to streamline processes, enhance compliance, and improve documentation quality.</li><li>Perform other quality-related duties as assigned to support evolving business and operational needs.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or another life science discipline.</li><li>Minimum of 5 years of work experience in an FDA-regulated industry, or a similar combination of education and experience.</li><li>Demonstrated understanding of quality management systems and relevant pharmaceutical regulations and regulatory guidance.</li><li>Experience supporting a cGMP biopharmaceutical manufacturing facility within a Quality organization.</li><li>Strong knowledge of current Good Manufacturing Practices (cGMP) and their application to manufacturing and testing operations.</li><li>Hands-on experience with material release, material disposition, and material management in a GMP environment.</li><li>Proficiency in quality review of batch records, manufacturing records, and associated release documentation.</li><li>Experience reviewing and managing deviations, investigations, change controls, CAPAs, and other quality events.</li><li>Familiarity with handling out-of-specification (OOS) investigations and related documentation.</li><li>Experience working with ERP systems, preferably NetSuite ERP, in support of materials management and quality processes.</li><li>Understanding of risk management principles and their application within a quality system, particularly for Phase 1 and first-in-human products and programs.</li><li>Strong communication skills, with the ability to convey complex quality and compliance concepts clearly to cross-functional partners and vendors.</li><li>Strong organizational skills and attention to detail, with the ability to manage multiple priorities in a fast-paced environment.</li><li>Demonstrated ability to work effectively and efficiently in a collaborative manner across multiple functional areas and external partners.</li><li>Commitment to collaborative values, accountability, continuous improvement, and solution-oriented thinking.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience with a vendor management program in a cGMP environment.</li><li>Experience in cGMP cell and gene therapy manufacturing and/or testing facilities.</li><li>Experience with PQ (Performance Qualification) testing in a GMP setting.</li><li>Familiarity with FDA expectations for advanced therapy and biologics manufacturing.</li><li>Comfort working in an emerging, innovation-driven biotech environment focused on novel immunotherapy platforms.</li><li>Ability to bring new ideas, support lean and continuous improvement initiatives, and contribute to a culture of innovation.</li><li>Proactive, communicative, and solution-oriented approach, with a focus on being accountable yet kind and collaborative.</li><li>Ability to gown aseptically and work in a cleanroom environment, if required.</li><li>Ability to work while gowned for extended periods of time, if required.</li><li>Ability to stand for extended periods of time to fulfill on-the-floor quality duties, if required.</li><li>Ability to work around laboratories, manufacturing areas, and equipment, including regular lifting of 10–20 lbs and occasional lifting of up to 50 lbs.</li><li>Ability to work occasional nights and weekends as needed to support operational demands.</li><li>Ability to primarily work onsite, with flexibility to work remotely when appropriate.</li></ul>Work EnvironmentThe role is primarily onsite at a state-of-the-art lentiviral vector development and manufacturing facility that supports cell and gene therapy manufacturing. The standard schedule is Monday through Friday, approximately 8:00 a.m. to 5:00 p.m., with general flexibility to support caretaking responsibilities such as childcare or school drop-off. Occasional night and weekend work may be required based on operational needs. The position operates in a collaborative, shared-resource model with QA Operations, Supply Chain, and Manufacturing, often described as a 'One QC' approach, emphasizing teamwork and cross-functional support. The environment includes laboratories, manufacturing suites, and cleanroom areas, where aseptic gowning and working while gowned for extended periods may be required. The role involves regular movement around labs and production areas, use of laboratory equipment, and handling of chemicals and biological materials. Team members may need to regularly lift 10–20 lbs and periodically up to 50 lbs. The culture emphasizes diversity, equity, inclusion, continuous improvement, innovation, and a strong sense of purpose in developing transformative cancer therapies, with a focus on collaborative, communicative, and solution-oriented work.Job Type &amp; LocationThis is a Contract position based out of Louisville, CO.Pay and BenefitsThe pay range for this position is $40.97 - $50.63/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 Louisville,CO.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 Assurance Specialist 3rd Shift Only Job DescriptionThe Quality Assurance Specialist supports production operations by spending the majority of their time on the manufacturing floor, performing verifications, walkthroughs, onsite reviews, and mini audits to ensure processes follow established procedures and regulatory requirements. This role also reviews and issues critical documentation, such as executed batch records, cleaning records, and logbooks, and helps identify and implement solutions when issues arise, including initiating deviations and supporting CAPA activities. The position combines hands-on floor presence with office-based documentation review and reporting.Responsibilities<ul><li>Spend approximately 60–70% of working time on the production floor supporting operations and verifying that activities comply with established procedures and quality standards.</li><li>Conduct routine walkthroughs of production areas to observe operations, identify potential issues, and ensure processes occur as intended.</li><li>Perform onsite reviews and mini audits to confirm adherence to GMP, FDA, ISO, and internal quality requirements.</li><li>Collaborate with operations personnel to identify problems, propose solutions, and help initiate deviations when necessary.</li><li>Review executed batch records, cleaning records, logbooks, and other quality-related documents for accuracy, completeness, and compliance.</li><li>Issue batch records as needed to support production activities and ensure proper documentation is in place before manufacturing.</li><li>Document findings from floor walkthroughs, reviews, and audits, and report observations to appropriate stakeholders in a clear and timely manner.</li><li>Support CAPA and document control activities related to quality events, deviations, and audit findings, as needed.</li><li>Follow area-specific gowning and safety requirements, ranging from safety shoes to full gowning, depending on the production area.</li><li>Use electronic quality management systems (EQMS) and other office tools to manage documentation, track activities, and maintain records.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in any science discipline preferred.</li><li>Experience in pharmaceutical manufacturing or a similar regulated production environment preferred.</li><li>Familiarity with FDA regulations and pharmaceutical quality systems preferred.</li><li>0–2+ years of experience in a regulated industry environment such as GMP, FDA, or ISO-regulated operations.</li><li>Experience or familiarity with batch records, batch record review, and document control practices.</li><li>Ability to work 12-hour shifts on a rotating schedule, including overnight hours for third shift.</li></ul>Work EnvironmentThis is an on-site role based primarily on the production floor, with the majority of time spent in manufacturing areas and the remainder in an office setting for documentation and reporting. Current openings are on third shift. New hires begin on first shift (Monday–Friday, 8:00 a.m. to 4:30 p.m.) for approximately 6–8 weeks of training, with efforts made to have team members on the same shift train together. The environment includes time on the production floor and time in an office area outside of production, with regular interaction with an electronic quality management system (EQMS) and other office tools. Job Type &amp; LocationThis is a Permanent position based out of Waunakee, WI.Pay and BenefitsThe pay range for this position is $62000.00 - $72000.00/yr.Eligible for Medical, Dental and Vision on day 1 of employment. 
The company provides Basic Life insurance, Basic AD&amp;D insurance along with Short-term disability on all full-time employees. 
Employees have the option to elect Voluntary Life, Voluntary AD&amp;D along with Long-term disability coverage. 
Health and Flexible spending account options. 
Full-time employees can contribute to their 401k upon hire and are eligible for a company contribution. 
Annually, the company offers 160 hours of vacation &amp; 40 hours of sick time (both pro-rated base on hire date) and 9 paid holidays.Workplace TypeThis is a fully onsite position in Waunakee,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 Assurance SpecialistJob DescriptionThe Quality Assurance Specialist provides day-to-day technical, quality, and operational support to pharmaceutical manufacturing operations. This role ensures that all production activities comply with cGMP standards, regulatory expectations, and safety requirements while supporting efficient, consistent, and high-quality output. The specialist works closely with cross-functional teams on the production floor to troubleshoot issues, maintain compliant documentation, and drive continuous improvement across processes and equipment.Responsibilities<ul><li>Provide floor-level technical support to manufacturing operators and supervisors to ensure smooth and compliant production activities.</li><li>Troubleshoot equipment issues, process deviations, and workflow bottlenecks to minimize downtime and maintain product quality.</li><li>Monitor production performance and assist with implementing corrective and preventive actions to address quality and operational concerns.</li><li>Prepare, revise, and maintain GMP documentation, including standard operating procedures (SOPs), batch records, logbooks, and related quality records.</li><li>Ensure adherence to FDA and other global regulatory requirements by supporting daily operations and documentation practices.</li><li>Support investigations into deviations and non-conformances, assist with CAPA development, and participate in change control processes.</li><li>Perform data collection, analysis, and review to support compliance, trend monitoring, and continuous improvement initiatives.</li><li>Partner with process control teams to support equipment qualification and validation activities in accordance with regulatory and internal standards.</li><li>Assist with process improvements, optimization initiatives, and technology transfers to enhance efficiency and product quality.</li><li>Support coordination of preventive and corrective maintenance activities with Engineering and Maintenance departments to maintain equipment reliability.</li><li>Train manufacturing personnel on procedures, new equipment, and process changes to ensure consistent understanding and execution.</li><li>Act as a subject matter liaison between Production, Quality, and Maintenance teams to facilitate clear communication and alignment.</li><li>Communicate production issues, progress updates, and risks to leadership in a timely and accurate manner.</li><li>Uphold and promote a strong culture of safety and compliance on the production floor, reinforcing best practices and expectations.</li><li>Participate in internal and external audits, walkthroughs, and safety reviews to support inspection readiness and continuous improvement.</li><li>Support environmental monitoring and compliance activities as needed to maintain controlled manufacturing environments.</li><li>Perform quality assurance activities such as in-process quality checks, inspections, and oversight of quality control practices.</li><li>Contribute to audit preparation and response efforts to ensure quality systems and processes remain robust and inspection-ready.</li></ul>Essential Skills<ul><li>1–3+ years of experience in a pharmaceutical, biotech, or other regulated manufacturing environment.</li><li>Working knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).</li><li>Understanding of applicable regulatory guidelines and expectations for regulated manufacturing.</li><li>Strong analytical and problem-solving skills with the ability to troubleshoot technical and process issues.</li><li>Excellent communication skills, both written and verbal, to support documentation, training, and cross-functional collaboration.</li><li>Strong documentation skills with attention to accuracy, completeness, and compliance.</li><li>Demonstrated ability to work effectively in a fast-paced, highly regulated environment.</li><li>Experience supporting quality assurance activities such as quality checks, inspections, and audits.</li><li>Familiarity with environmental monitoring and quality control concepts in manufacturing settings.</li><li>High attention to detail and accuracy in all aspects of work.</li><li>Technical troubleshooting skills related to processes, equipment, and production workflows.</li><li>Strong collaboration and cross-functional communication skills to work with Production, Quality, Engineering, and Maintenance teams.</li><li>Effective time management and prioritization skills to handle multiple tasks and deadlines.</li><li>A continuous improvement mindset with a strong focus on compliance and quality.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in sterile or aseptic operations and biologics manufacturing.</li><li>Knowledge of Six Sigma or other continuous improvement methodologies.</li><li>Familiarity with batch records, inventory management systems, and Laboratory Information Management Systems (LIMS).</li><li>Experience participating in or supporting internal and external audits.</li><li>in quality assurance, including quality control, quality checks, and inspection activities.</li><li>Exposure to environmental monitoring programs within cleanroom or controlled environments.</li><li>Ability to serve as a trainer for manufacturing personnel on procedures, equipment, and process changes.</li><li>Comfort working with cross-functional teams to support equipment qualification, validation, and process optimization.</li></ul>Work EnvironmentThis role is primarily on-site within pharmaceutical manufacturing areas, including cleanrooms and other controlled environments. Work in classified areas requires appropriate gowning and adherence to strict hygiene and contamination control procedures. The typical first-shift production schedule consists of four 10-hour days, with standard hours from 6:00 AM to 4:30 PM. Candidates must be available for various days of the week and may be scheduled on a 5-day workweek as needed. Occasional off-shift or weekend support may be required during critical operations. The environment is highly regulated and safety-focused, with close collaboration between Production, Quality, Engineering, and Maintenance teams and regular use of GMP documentation, electronic systems, and monitoring tools.Job Type &amp; LocationThis is a Permanent position based out of Syracuse, NY.Pay and BenefitsThe pay range for this position is $52000.00 - $62400.00/yr.Company Benefits
Company Benefits
Company Benefits
Company Benefits
• 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 Syracuse,NY.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.

Description
					Provide quality oversight for manufacturing operations, ensuring compliance with cGMP regulations and internal procedures.
Review and disposition raw materials, plasmids, drug substance, and drug product batches.
Review and approve batch production records, testing records, and manufacturing documentation.
Support batch record review and release activities for materials and products.
Review, investigate, and document deviations, ensuring appropriate corrective and preventive actions are implemented.
Author, review, and revise SOPs, batch records, policies, and training materials.
Participate in real-time quality oversight activities within manufacturing operations and cleanroom environments.
Partner with cross-functional teams to support manufacturing readiness, startup activities, and continuous improvement initiatives.
Ensure adherence to data integrity principles and training requirements.
Monitor manufacturing operations for compliance with established specifications and procedures.
Support internal audits and regulatory inspection readiness activities.
Escalate quality, manufacturing, and safety concerns as appropriate.
Serve as a subject matter expert (SME) and mentor for new team members.
Lead and contribute to quality and compliance-related projects across multiple functional groups.
Drive root cause investigations and corrective actions for complex quality issues.
										Skills
					Quality assurance, drug substance, drug product, Batch record, raw materials, deviations, change control, environmental monitoring, microbioloigcal testing, Batch record review, Authoring SOPs, Sop, audit, compliance
										Top Skills Details
					Quality assurance,drug substance,drug product,Batch record,raw materials,deviations,change control,environmental monitoring,microbioloigcal testing,Batch record review
										Additional Skills &amp; Qualifications
					BS or equalivalent experience with in science industry within quality assurance
 2-5 Years experience 
Knowledge of FDA, EU, ICH guidelines, and relevant regulations.
Experience with quality systems, including batch record review, deviation management, and change control.
Proficiency in authoring and reviewing GMP documentation.
Familiarity with environmental monitoring and microbiological testing.
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Contract position based out of Norwood, MA.Pay and BenefitsThe pay range for this position is $42.00 - $52.00/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 Norwood,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.

<h3>Supplier Quality Specialist</h3>Location: Westborough, MASchedule: Monday - Friday Industry: Biotechnology / Pharmaceutical Manufacturing<h4>About the Role</h4>We are seeking a Supplier Quality Specialist to support supplier quality and compliance activities within a regulated manufacturing environment. This role will work closely with internal stakeholders and external suppliers to ensure materials, services, and vendors meet established quality, regulatory, and business requirements.The ideal candidate will have experience supporting supplier qualification, audits, CAPA activities, quality systems, and supplier performance management within a GMP-regulated environment.<h4>Responsibilities</h4><ul><li>Support the qualification, onboarding, and ongoing management of suppliers, vendors, and service providers.</li><li>Maintain supplier quality documentation, including qualification records, quality agreements, audit reports, and supporting documentation.</li><li>Coordinate supplier assessments, audits, and periodic supplier evaluations.</li><li>Participate in supplier audits and review documentation related to quality systems, compliance, and corrective actions.</li><li>Collaborate with sourcing, procurement, quality, operations, and other cross-functional teams to support supplier-related activities.</li><li>Manage supplier communication processes and support supplier change management initiatives.</li><li>Review supplier notifications and coordinate cross-functional impact assessments.</li><li>Monitor supplier performance metrics and track quality-related issues.</li><li>Support investigation, documentation, and follow-up of supplier CAPAs and corrective action plans.</li><li>Maintain accurate records within quality systems and tracking tools.</li><li>Drive timely closure of supplier quality action items and commitments.</li><li>Support continuous improvement initiatives focused on supplier quality, risk mitigation, compliance, and operational excellence.</li></ul><h4>Qualifications</h4><ul><li>Bachelor's degree in Engineering, Life Sciences, Chemistry, Biology, or a related technical discipline, or equivalent experience.</li><li>2–5 years of experience in a regulated manufacturing, quality, supplier quality, or technical operations environment.</li><li>Experience supporting supplier qualification, supplier assessments, supplier audits, and vendor management programs.</li><li>Working knowledge of GMP, GxP, quality systems, and regulatory requirements.</li><li>Experience with CAPA, change control, deviation management, and supplier performance monitoring.</li><li>Strong organizational skills with the ability to manage multiple priorities and deadlines.</li><li>Excellent communication and cross-functional collaboration skills.</li></ul><h4>Preferred Qualifications</h4><ul><li>Experience participating in or leading supplier, internal, or external audits.</li><li>Knowledge of risk management methodologies and continuous improvement principles.</li><li>Experience supporting advanced manufacturing technologies or pharmaceutical/biotech operations.</li><li>Familiarity with quality management systems and supplier quality software tools.</li></ul>If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. Job Type &amp; LocationThis is a Contract to Hire position based out of Westborough, MA.Pay and BenefitsThe pay range for this position is $38.00 - $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 Westborough,MA.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 Assurance Specialist – Supplier Quality

DescriptionSupport the qualification and onboarding of external suppliers, vendors, and service providers to meet business and operational needs.Maintain supplier quality and compliance documentation, including qualification records, agreements, and supporting documentation.Coordinate and support the planning, scheduling, and tracking of supplier assessments and periodic evaluations.Participate in supplier assessments and review documentation associated with quality, compliance, and corrective actions.Collaborate cross-functionally with internal stakeholders across operations, sourcing, procurement, quality, and other business functions.Administer supplier communication and change management processes.Review supplier notifications and coordinate cross-functional impact assessments.Support evaluation and implementation of supplier-related changes as needed.Monitor supplier performance and corrective action activities.Maintain tracking systems and documentation associated with supplier quality issues and corrective actions.Drive follow-up activities and ensure timely completion of action items and commitments.Support continuous improvement initiatives related to supplier management, risk mitigation, and quality systems.Skillsvendor management, Gmp, Quality assurance, supplier audit, supplier management, Capa, Audit, Batch recordTop Skills Detailsvendor management,Gmp,Quality assurance,supplier audit,supplier managementAdditional Skills &amp; QualificationsBachelor’s degree in a scientific, engineering, or related technical discipline, or an equivalent combination of education, training, and professional experience. Experience with advanced manufacturing technologies is a plus.2–5 years of experience in a regulated industry environment, quality organization, manufacturing operation, or related technical setting is required.Experience supporting supplier quality activities, including supplier qualification and assessments, performance monitoring, corrective and preventive action (CAPA) management, and change control processes.Working knowledge of applicable GxP regulations, quality systems, and industry standards.Experience participating in or leading internal, external, or supplier audits.Strong understanding of quality management principles, risk assessment methodologies, and continuous improvement practices.Excellent organizational, communication, and cross-functional collaboration skills.Job Type &amp; LocationThis is a Contract to Hire position based out of Framingham, MA.Pay and BenefitsThe pay range for this position is $38.00 - $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 Framingham,MA.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.

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