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

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

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



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



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



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



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



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

public

Quality Engineer

<h1>Job Title: Quality Engineer</h1>Job DescriptionWe are seeking a Quality Engineer who will identify root causes through corrective and preventive actions, implement and validate these plans, and oversee the quality management system. The role involves improving production methods, product quality, and equipment performance. You will be responsible for data collection, entry, and reporting for product conformance and process capability, and for developing and implementing methods and standards for products, materials, equipment, returns, testing, calibration, and processes. Support for AS9100 and ISO 9001 quality management standards, utilizing statistical process control, and supporting mechanical and electrical testing are also key aspects of this role. Our products support multiple industries such as Aerospace/Defense and Medical device. Responsibilities<ul><li>Identify root causes through corrective and preventive actions</li><li>Implement and validate corrective and preventive action plans</li><li>Oversee the quality management system</li><li>Improve production methods, product quality, and equipment performance</li><li>Collect, enter, and report data for product conformance and process capability</li><li>Develop and implement methods and standards for products, materials, equipment, returns, testing, calibration, and processes</li><li>Support AS9100 and ISO 9001 quality management standards</li><li>Utilize statistical process control to support process capability</li><li>Support mechanical and electrical testing</li><li>Execute gap analysis</li></ul>Essential Skills<ul><li>Bachelor's Degree in a related discipline preferred</li><li>2+ years of experience within a quality function</li><li>Working knowledge and experience with problem-solving methodologies</li><li>Experience with quality management systems</li><li>Skills in quality function management</li><li>Continuous improvement and lean/six sigma methodologies</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with root cause analysis and corrective action plans</li></ul>Work EnvironmentYou will report to the Quality Manager and work within a group of engineers and technicians. Our company is a leader in connectors and cables for fiber optics, supporting regulated environments such as government, aerospace, defense, medical, and industrial sectors. This role requires U.S. citizenship, as we cannot provide visa sponsorship. Our work culture promotes growth within the quality and other departments, and we offer a tuition reimbursement program once you are direct with the organization.#mneng26Job Type &amp; LocationThis is a Permanent position based out of Owatonna, MN.Pay and BenefitsThe pay range for this position is $70000.00 - $90000.00/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
• 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 Owatonna,MN.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 EngineerJob DescriptionThe Quality Engineer will execute quality control activities within a fabrication shop supporting microelectronics capital projects. This engineering role focuses on ensuring products meet stringent quality standards the first time, with minimal rework or delays. The position requires an experienced, forward-thinking quality professional who contributes actively as a member of the Quality Team and helps secure the expected quality of all fabricated products.Responsibilities<ul><li>Execute quality control activities in a fabrication shop environment for microelectronics capital projects.</li><li>Ensure products meet defined quality requirements on the first pass, minimizing rework, defects, and schedule delays.</li><li>Perform welding inspections to verify compliance with applicable standards and specifications.</li><li>Review and interpret blueprints, mechanical drawings, and structural documentation to validate quality criteria.</li><li>Apply ISO 9001 principles and procedures to maintain and improve the quality management system.</li><li>Conduct supplier audits to assess and monitor supplier quality performance and adherence to standards.</li><li>Support and perform quality assurance activities throughout the production process.</li><li>Identify, investigate, and document nonconformities and quality issues.</li><li>Lead or participate in root cause analysis to determine underlying causes of defects or process deviations.</li><li>Recommend and help implement corrective and preventive actions to improve product and process quality.</li><li>Collaborate with engineering, production, and other cross-functional teams to resolve quality-related concerns.</li><li>Contribute to continuous improvement initiatives, leveraging Six Sigma tools and methodologies where applicable.</li><li>Maintain accurate quality records, inspection reports, and audit documentation.</li><li>Support a culture of quality and accountability within the fabrication shop and broader project teams.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience in quality engineering.</li><li>Hands-on experience with quality engineering in a fabrication or manufacturing environment.</li><li>Strong knowledge of ISO 9001 and its application within a quality management system.</li><li>Experience performing welding inspections and evaluating weld quality.</li><li>Ability to read and interpret blueprints, mechanical drawings, and structural documents.</li><li>Proficiency in quality assurance practices and quality control methodologies.</li><li>Experience conducting supplier audits and assessing supplier quality performance.</li><li>Proven ability to perform root cause analysis and develop effective corrective actions.</li><li>Familiarity with Six Sigma principles; Six Sigma Green Belt certification preferred.</li><li>Attention to detail and strong analytical and problem-solving skills.</li><li>Effective communication skills to collaborate with cross-functional teams and document findings clearly.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certified Welding Inspector (CWI) or AWS certification is a strong plus.</li><li>Experience in microelectronics or capital project environments is beneficial.</li><li>Experience in mechanical or structural fabrication quality is advantageous.</li><li>Demonstrated ability to support continuous improvement initiatives using Six Sigma tools.</li><li>Strong organizational skills and ability to manage multiple quality activities simultaneously.</li><li>Forward-thinking mindset with a focus on improving processes and preventing defects.</li><li>Interest in professional growth and taking on increasing responsibility over time.</li></ul>Work EnvironmentThis role is primarily based in a cubicle office setting, with regular collaboration across engineering and production teams. The Quality Engineer will spend occasional time on the fabrication shop floor to conduct inspections, audits, and investigations, and may travel domestically on a minimal basis for supplier visits or project needs. The environment supports complex and technically interesting projects in the microelectronics capital space, offering opportunities for growth and involvement in impactful, high-visibility work.Job Type &amp; LocationThis is a Permanent position based out of Brooklyn Park, MN.Pay and BenefitsThe pay range for this position is $90000.00 - $105000.00/yr.Strong Internal Company Benefits. If you have any questions or wish to see a copy of the benefits, please feel free to reach out.Workplace TypeThis is a fully onsite position in Brooklyn Park,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.

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

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

Description<ul><li>Implement interim and permanent corrective actions to resolve quality issues using 8D tool, 6 panel, etc.</li><li>Manage and direct statistical process control activities</li><li>Knowledge of and ability to execute measurement systems analysis &amp; variable data analysis</li><li>Identify sources of variation within a production environment effectively and efficiently</li><li>Establish tolerance limits and facilitate appropriate corrective actions</li><li>Establish and monitor quality target levels for each build</li><li>Provide input for design and assembly concepts which will yield nominal variations</li><li>Establish critical characteristics for gauging and measuring data collection methods</li><li>Determine inspection equipment and facility requirements </li><li>Support expedited concern resolution with cross functional teams including the Quality Department, Production and Suppliers</li><li>Review internal/external suppliers for critical characteristics process compatibility</li><li>Review incoming quality concerns to maintain quality with assigned area; must have experience with initiating containment, determining root cause and implementing corrective actions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Minimum of five years of manufacturing or quality experience</li><li>Ability to work independently and make decisions with minimal supervision</li><li>Ability to lead cross-functional groups to resolve concerns</li><li>Strong written and oral communication skills: you will be speaking or presenting to leadership or representing company while engaging with 3rd party suppliers</li><li>High level of analytical and statistical skills to trend quality data and take appropriate actions</li><li>Ability to positively influence change</li><li>Ability to handle complex issues and multi-taskin</li><li>Strong organizational skills</li><li>Proficiency in using Outlook, Excel, and PowerPoint. Understanding of the concepts and principles surrounding Business Objects, SharePoint</li></ul>Job Type &amp; LocationThis is a Contract position based out of Sterling Heights, MI.Pay and BenefitsThe pay range for this position is $42.30 - $46.53/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 Sterling Heights,MI.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.

<h3>Quality Engineer</h3>Summary:Responsible for maintaining and improving quality systems, leading root cause investigations and CAPA activities, supporting new product introductions, and ensuring compliance with ISO 13485 (medical device) and regulatory requirements.Requirements:<ul><li>Bachelor's degree in Engineering or related field</li><li>3-5+ years of Quality Engineering experience, preferably in medical devices</li><li>Experience with QMS, CAPA, root cause analysis, SPC, and risk management</li><li>Knowledge of ISO 13485 and manufacturing processes</li><li>Proficient with Minitab, Excel, and ERP systems (SAP/Oracle preferred)</li></ul>Preferred:<ul><li>ASQ certification</li></ul>Job Type &amp; LocationThis is a Contract position based out of Waukegan, IL.Pay and BenefitsThe pay range for this position is $42.00 - $46.00/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 Waukegan,IL.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 EngineerJob DescriptionThe Quality Engineer owns and drives Corrective and Preventive Action (CAPA) activities end-to-end, manages Non-Conforming Material Reports (NCMRs), and supports design quality across the product lifecycle with a focus outside manufacturing operations. This role operates with a strong sense of urgency to resolve quality events, identifies and addresses gaps in quality processes, and collaborates closely with Engineering, Regulatory, and Operations teams to improve product quality and patient outcomes. The position offers the opportunity to take ownership of quality initiatives, build and refine processes, and grow within a collaborative, mission-driven environment.Responsibilities<ul><li>Own and drive CAPA activities from initial investigation through root cause analysis, implementation of corrective and preventive actions, and formal closure.</li><li>Manage and resolve Non-Conforming Material Reports (NCMRs), ensuring appropriate disposition and documentation.</li><li>Support design quality efforts across the product lifecycle, with a primary focus on activities outside of manufacturing operations.</li><li>Collaborate cross-functionally with Engineering, Regulatory, and Operations to investigate and resolve quality issues and ensure alignment on quality standards.</li><li>Identify gaps in existing quality processes and proactively propose, develop, and implement improvements.</li><li>Operate with a strong sense of urgency to ensure timely resolution of quality events and minimize impact on products and patients.</li><li>Balance hands-on execution and effective delegation, while remaining directly involved in technical quality work as needed.</li><li>Independently manage quality investigations and CAPA tasks with limited direction, maintaining high standards of documentation and compliance.</li><li>Support both technical execution and process ownership for quality systems and initiatives.</li><li>Contribute to building and refining quality processes in a fast-paced, evolving environment.</li></ul>Essential Skills<ul><li>2–6+ years of experience in Quality Engineering within medical devices or a regulated industry.</li><li>Hands-on experience independently managing CAPAs and conducting quality investigations.</li><li>Experience working with Non-Conforming Material Reports (NCMRs).</li><li>Exposure to design quality principles, with focus not strictly limited to manufacturing or operations.</li><li>Strong problem-solving skills and the ability to think critically through complex quality issues.</li><li>Proven ability to work independently with limited direction while maintaining accountability for results.</li><li>Excellent communication skills, with the ability to clearly convey technical information to cross-functional partners.</li><li>Demonstrated cross-functional collaboration skills with Engineering, Regulatory, and Operations teams.</li><li>Comfort working in fast-paced, evolving environments with a degree of ambiguity.</li><li>Demonstrated ability to quickly ramp up and hit the ground running in new roles.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in a Contract Manufacturer (CMO) or small to mid-sized medical device company.</li><li>Prior experience supporting both technical execution and ownership of quality processes.</li><li>Motivation to build and improve quality processes in a growing, innovative organization.</li><li>Interest in contributing to product quality and patient outcomes in a mission-driven setting.</li><li>Ability to balance detailed technical work with broader process improvement initiatives.</li><li>Eligibility for equity upon full-time conversion, subject to company policies.</li></ul>Work EnvironmentThe role is based in a growing, innovative medical device environment that is fast-paced and evolving, with a culture that values ownership, collaboration, and mission-driven work focused on improving patient outcomes. The team operates with core collaboration hours from 9:00 AM to 3:00 PM, offering flexibility outside of those hours to support work-life balance. You will work closely with Engineering, Regulatory, and Operations in a highly cross-functional setting, with an emphasis on both technical quality execution and continuous process improvement. The organization uses a work model designed to ensure mutual fit, allowing you to grow into full-time opportunities and potentially participate in equity programs upon conversion.Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Paul, MN.Pay and BenefitsThe pay range for this position is $45.00 - $60.00/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 Paul,MN.Application DeadlineThis position is anticipated to close on Aug 5, 2026.About Actalent 

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



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



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



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



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



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

Quality Engineer / CMM ProgrammerJob DescriptionWe are seeking a skilled Quality Engineer / CMM Programmer with expertise in operating and programming Faro Arm CMM using Polyworks software. The ideal candidate should be able to program CMM using PC-DMIS software, particularly offline, and work with CAD models without requiring a physical part or 2D print.Responsibilities<ul><li>Operate and program Faro Arm CMM with Polyworks software.</li><li>Program CMM using PC-DMIS software, especially offline.</li><li>Mount, install, align, and secure tools, attachments, fixtures, and workpieces on CMM machine using hand tools and precision measuring instruments.</li><li>Measure dimensions of components and finished products to ensure conformance to specifications using precision measuring instruments, templates, and fixtures.</li><li>Read and write CMM reports accurately.</li><li>Develop work instructions for CMM setup and operation for various programs.</li><li>Use calipers, height gauges, micrometers, and various other hand tools.</li><li>Ensure accuracy and precision in measurements for sample layouts and production for first piece and dimensional checks.</li><li>Assist the Quality Director in dimensional inspection of products for PPAPs and investigations.</li><li>Collect and analyze data for measurement systems analysis, capability studies, design of experiments, and gauge R&amp;R.</li><li>Review acceptance criteria defined by customer documents to ensure appropriate inspection methods and identify and document any drawing/specification errors.</li><li>Compile and submit First Article Inspection Reports (FAIR) to customers for approval.</li><li>Assist the Quality Director in defining and delivering responses to customer requests and inquiries related to product quality.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Lake Forest, IL.Pay and BenefitsThe pay range for this position is $70000.00 - $80000.00/yr.Company benefits include 401K, medical, dental, visionWorkplace TypeThis is a fully onsite position in Lake Forest,IL.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 Engineer / CMM Programmer

Quality Engineer II (Contract)Job DescriptionThe Quality Engineer II is a skilled quality assurance professional with extensive experience in quality or manufacturing within a highly regulated industry. This role focuses on evaluating and improving production processes and performance in manufacturing, with a strong emphasis on contamination and cross-contamination understanding, aseptic practices, and compliance inspections. This position plays a critical role in supporting manufacturing by providing quality input, initiating deviations, and ensuring the production and release of quality bulk drug substances for clinical and commercial clients.Responsibilities<ul><li>Oversee activities and provide QA-related input.</li><li>Collaborate with cross-functional teams to develop, optimize, and improve processes to enhance efficiency, productivity, and quality.</li><li>Conduct thorough audits and inspections to ensure sustained compliance with industry standards and regulations.</li><li>Observe aseptic practices and provide immediate coaching to site colleagues to prevent contamination and cross-contamination.</li><li>Participate in client and regulatory audits as a Subject Matter Expert (SME) on Fit and Finish, Changeover, and Change Control procedures.</li><li>Observe critical process steps to ensure adherence to guiding procedures, batch records, and established aseptic practices.</li><li>Perform daily GEMBAs of manufacturing areas and provide immediate feedback to ensure compliance with cGMPs, site procedures, and regulatory requirements.</li><li>Perform QA approval of suite and equipment changeover between client processes.</li><li>Conduct autoclave logbook review and facilitate corrections.</li><li>Perform Fit and Finish inspections per risk assessment and guiding procedures.</li><li>Perform monthly aseptic observations of critical activities in Biosafety Cabinets.</li><li>Attend and actively participate in Manufacturing and QA OTF Tier 1 huddles.</li><li>Act as Quality Management Representative as needed.</li><li>Develop personal knowledge and skills in quality standards.</li><li>Provide training, coaching, and mentorship to new and less experienced team members on quality standards.</li><li>Qualify new team members for tasks requiring QSME training.</li><li>Write and review deviations in Trackwise.</li><li>Author, revise, and review procedures in eDMS.</li><li>Write and implement CAPAs as needed.</li><li>Conduct and participate in investigation interviews/RAPIDs.</li></ul>Essential Skills<ul><li>Quality assurance expertise.</li><li>Inspection and auditing skills.</li><li>GMP and FDA pharmaceutical QA experience.</li><li>On-floor QA oversight over processes.</li><li>CAPA management.</li><li>SOP and batch record experience.</li><li>Root cause analysis.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's Degree in Life Sciences (biology, chemistry, biochemistry) or a related field with a minimum of three years of relevant experience.</li><li>Cleanroom manufacturing experience preferred.</li><li>Non-science degrees considered with a minimum of seven years of directly related experience.</li><li>Understanding of quality practices and cGMP regulations.</li><li>Experience with investigational writing software (Trackwise) and root cause analysis tools.</li><li>Technical writing skills and proficiency with document management software.</li><li>Tech transfer experience is a plus.</li><li>Experience with Lean Manufacturing and Six Sigma methodologies is a plus.</li><li>Excellent problem-solving and analytical skills.</li></ul>Work EnvironmentThe work involves spending 80% of the time in a cleanroom environment, requiring full gowning (bodysuit, gloves, hair &amp; beard nets, face covers, safety glasses) and meeting cleanroom gowning requirements. The remaining 20% involves desk work. The role operates on a 2nd shift from 2 PM to 12:30 AM, with rotating 10-hour shifts. Employees must be able to lift a minimum of 25 lbs independently and stand for 80% of the shift.Job Type &amp; LocationThis is a Contract position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $33.00 - $38.46/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 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 Engineer II (Contract)

Job Description: Quality Engineering ManagerThe Quality Engineering Manager leads the development, implementation, and maintenance of robust quality standards for industrial processes, materials, and products across diverse markets such as aerospace, automotive, medical, energy, robotics, and industrial machinery. This role oversees both Quality Control and Quality Assurance functions, ensuring consistent delivery of high-quality products, continuous improvement of processes, and exceptional service to customers. The manager provides strategic direction to the quality organization, drives best practices in quality engineering and inspection, and ensures that quality systems and teams effectively support both new and existing customers.Responsibilities<ul><li>Plan, direct, and oversee activities related to the development, application, and maintenance of quality standards for industrial processes, materials, and products.</li><li>Lead and manage Quality Control and Quality Assurance activities to ensure consistent product quality and compliance with customer and industry requirements.</li><li>Manage staff resources and organizational structure within the Quality Engineering Department to align with business objectives for new and existing customers.</li><li>Identify opportunities to improve Quality Engineering Department processes and implement best practices to enhance efficiency and effectiveness.</li><li>Review and improve Inspection Department processes, ensuring the adoption and maintenance of best practices.</li><li>Maintain and oversee the Customer Issue Report, ensuring issues are accurately documented, tracked, and resolved.</li><li>Coordinate and monitor the Returned Goods Authorization (RGA) process and status, ensuring timely handling and resolution of returned products.</li><li>Lead the Material Review Board (MRB), including scheduling and conducting reviews of discrepant hold areas and making disposition decisions.</li><li>Manage the Corrective Action System, including identifying root causes, defining corrective actions, verifying effectiveness, and ensuring completeness and accuracy of all related information.</li><li>Oversee the Late Shipment System and ensure appropriate actions are taken to address and reduce late deliveries.</li><li>Gain a comprehensive understanding of the total work volume handled by the Quality Department, including QC40 tickets, late shipments, RGAs, and related activities on a monthly, quarterly, and yearly basis.</li><li>Develop and implement strategies to address unfavorable quality trends, with the goal of reducing the frequency and quantity of quality issues.</li><li>Maintain and manage budgetary spending within the Quality Engineering Department, ensuring alignment with financial objectives.</li><li>Monitor and mentor Quality Engineering and Inspection leaders on departmental spending, ensuring adherence to approved and adjusted budgets.</li><li>Monitor the Quality Engineering Phone Loop to verify that the ACD phone system is properly staffed during business hours, report weekly results, and develop plans to correct any significant variances.</li><li>Review and provide input on financial budgets for the Quality Engineering Department, suggesting ideas to optimize resource utilization.</li><li>Lead, motivate, and inspire direct reports, fostering a high-performance, collaborative, and continuous-improvement culture.</li><li>Monitor and review the performance of direct reports, providing timely and objective coaching, mentoring, and counseling.</li><li>Resolve performance, job satisfaction, and interpersonal issues within the team, balancing employee needs with departmental and organizational goals.</li><li>Develop onboarding and training programs for Quality Engineering and Inspection staff, and guide the creation of individual development plans.</li><li>Manage the quality engineering team, including involvement in recruitment, selection, and development of team members.</li></ul>Essential Skills<ul><li>Four-year Bachelor of Science degree in Engineering from an accredited four-year college or university.</li><li>Five to ten years of related experience in quality engineering or a closely related field.</li><li>Minimum of seven years of experience in a role supervising quality engineers.</li><li>Proven experience implementing Quality Management Systems (QMS), including system deployment, maintenance, and continuous improvement.</li><li>Strong experience in Supplier Quality Assurance and quality auditing.</li><li>In-depth understanding of APQP (Advanced Product Quality Planning) and PPAP (Production Part Approval Process).</li><li>Proficiency in Gage Repeatability &amp; Reproducibility (Gage R&amp;R) studies.</li><li>Experience with Statistical Process Control (SPC) and capability charts.</li><li>Knowledge and practical experience with AS9102 and Industrial Validation Documents.</li><li>Experience with S1002s, First Article Inspection Reports, Process Failure Mode and Effects Analysis (PFMEA), Process Flow Diagrams, and Control Plans.</li><li>Strong understanding of ISO 9001 quality management standards.</li><li>Knowledge of IATF 16949 automotive quality management requirements.</li><li>Knowledge of AS9100 aerospace quality management standards.</li><li>Minitab experience for statistical analysis and data-driven decision making.</li><li>Ability to work permanently in the United States (authorization to work in the US on a permanent basis).</li></ul>Additional Skills &amp; Qualifications<ul><li>Black Belt certification preferred, indicating advanced skills in process improvement and problem solving.</li><li>Experience in the medical field preferred, particularly in environments governed by stringent regulatory and quality requirements.</li><li>Experience working within ISO 9000 and ISO 9001 quality management frameworks.</li><li>Demonstrated ability to lead and develop teams, including coaching, mentoring, and performance management.</li><li>Strong analytical and problem-solving skills, with the ability to interpret complex data and drive corrective and preventive actions.</li><li>Excellent communication skills, with the ability to collaborate effectively across departments and with customers.</li><li>Experience managing budgets and financial planning for departmental operations.</li><li>Proven ability to design and implement onboarding, training, and development programs for technical and quality-focused teams.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Deer Park, IL.Pay and BenefitsThe pay range for this position is $120000.00 - $135000.00/yr.5.5% 401k company Match. Everything else available upon an offerWorkplace TypeThis is a fully onsite position in Deer Park,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 Engineering Manager

Quality Engineering Technicians NeededHelp Build the Future of Electric Vehicles!Join an innovative team at the forefront of EV manufacturing as a 2nd Shift Quality Technician (GA/Chassis/Battery). In this hands-on role, you'll be responsible for ensuring the quality, safety, and performance of cutting-edge electric vehicle systems. If you're passionate about quality, problem-solving, and making an impact in a fast-paced production environment, this is your opportunity to be part of a company transforming the future of transportation.Responsibilities<ul><li>Conduct quality inspections on vehicles to ensure compliance with standards.</li><li>Implement quality control measures to improve production processes.</li><li>Collaborate with cross-functional teams to enhance product reliability.</li><li>Maintain and calibrate test equipment.</li><li>Prepare test data and identify areas for quality control improvement.</li></ul>Essential Skills<ul><li>Troubleshooting and use of test equipment.</li><li>Experience in quality inspections, especially in the automotive or aerospace industry.</li><li>Proficiency in data analysis software.</li><li>Strong skills in Microsoft Office applications such as PowerPoint, Word, and Excel.</li><li>Experience in quality control, quality assurance, and electronics.</li><li>Ability to conduct root cause analysis.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience in quality control or assurance in a manufacturing environment, preferably in the automotive industry.</li><li>3+ years of experience in a related field.</li><li>Proficient in using inspection and testing equipment like calipers, micrometers, and multimeters.</li><li>Strong analytical and problem-solving skills.</li></ul>Work EnvironmentThe position will initially start on the 1st shift for 1-2 months, transitioning to the 2nd shift. Flexibility to work mandatory overtime and Saturdays is required. The role requires physical fitness and experience working on large vehicle structures.Job Type &amp; LocationThis is a Contract position based out of Garden Grove, CA.Pay and BenefitsThe pay range for this position is $25.00 - $32.00/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 Garden Grove,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 Engineering Technician

Quality Engineering Technicians NeededHelp Build the Future of Electric Vehicles!Join an innovative team at the forefront of EV manufacturing as a 2nd Shift Quality Technician (GA/Chassis/Battery). In this hands-on role, you'll be responsible for ensuring the quality, safety, and performance of cutting-edge electric vehicle systems. If you're passionate about quality, problem-solving, and making an impact in a fast-paced production environment, this is your opportunity to be part of a company transforming the future of transportation.Responsibilities<ul><li>Conduct quality inspections on vehicles to ensure compliance with standards.</li><li>Implement quality control measures to improve production processes.</li><li>Collaborate with cross-functional teams to enhance product reliability.</li><li>Maintain and calibrate test equipment.</li><li>Prepare test data and identify areas for quality control improvement.</li></ul>Essential Skills<ul><li>Troubleshooting and use of test equipment.</li><li>Experience in quality inspections, especially in the automotive or aerospace industry.</li><li>Proficiency in data analysis software.</li><li>Strong skills in Microsoft Office applications such as PowerPoint, Word, and Excel.</li><li>Experience in quality control, quality assurance, and electronics.</li><li>Ability to conduct root cause analysis.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience in quality control or assurance in a manufacturing environment, preferably in the automotive industry.</li><li>3+ years of experience in a related field.</li><li>Proficient in using inspection and testing equipment like calipers, micrometers, and multimeters.</li><li>Strong analytical and problem-solving skills.</li></ul>Work EnvironmentThe position will initially start on the 1st shift for 1-2 months, transitioning to the 2nd shift. Flexibility to work mandatory overtime and Saturdays is required. The role requires physical fitness and experience working on large vehicle structures.Job Type &amp; LocationThis is a Contract position based out of Garden Grove, CA.Pay and BenefitsThe pay range for this position is $25.00 - $32.00/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 Garden Grove,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: Quality Engineering TechnicianJob DescriptionThe Quality Engineering Technician leads inspection activities across incoming, in-process, and final inspection within a regulated aerospace and defense manufacturing environment. This role ensures strict compliance with AS9100 standards, customer specifications, and internal procedures while mentoring junior inspectors and supporting root cause investigation and corrective action implementation. The position plays a key role in maintaining product quality, driving continuous improvement, and upholding regulatory and customer requirements.Responsibilities<ul><li>Lead incoming, in-process, and final inspection activities for aerospace and defense components and assemblies.</li><li>Ensure all inspection work complies with AS9100 requirements, customer specifications, and internal quality procedures.</li><li>Read and interpret engineering drawings and blueprints, including GD&amp;T tolerancing, using CREO, CAD, and related tools.</li><li>Perform detailed mechanical inspections using calipers, gauges, micrometers, and other metrology equipment.</li><li>Conduct First Article Inspections (FAI) and document results in accordance with applicable standards and customer requirements.</li><li>Identify, document, and process nonconforming material, including generating Non-Conformance Reports (NCRs).</li><li>Support and lead root cause analysis activities for nonconformances and quality issues.</li><li>Participate in and support Corrective and Preventive Action (CAPA) processes to address quality problems and prevent recurrence.</li><li>Analyze GD&amp;T requirements to verify dimensional compliance and ensure proper interpretation of tolerances.</li><li>Collaborate with production, engineering, and quality teams to resolve quality issues and improve processes.</li><li>Mentor and guide junior inspectors, providing training and support on inspection techniques, tools, and quality procedures.</li><li>Utilize quality assurance and quality control best practices to maintain consistent inspection standards.</li><li>Support final inspection activities to verify that products meet all contractual, regulatory, and customer requirements prior to shipment.</li><li>Contribute to continuous improvement initiatives, including Six Sigma or Lean Manufacturing activities where applicable.</li><li>Maintain accurate inspection records, reports, and documentation in accordance with internal and external requirements.</li><li>Assist with or perform CMM inspections if experienced with CMM operation and programming.</li><li>Ensure adherence to applicable aerospace and defense regulations, including ITAR and DFARS, where required.</li></ul>Essential Skills<ul><li>2+ years of quality inspection experience</li><li>Strong knowledge of Geometric Dimensioning and Tolerancing (GD&amp;T) and blueprint reading.</li><li>Experience working in AS9100-regulated environments and familiarity with related standards such as AS9102.</li><li>Proficiency in mechanical inspection using calipers, gauges, micrometers, and other metrology tools.</li><li>Ability to read and interpret engineering drawings and blueprints in CREO, CAD, AutoCAD, and similar platforms.</li><li>Hands-on experience with incoming, in-process, and final inspection of parts and assemblies.</li><li>Experience performing First Article Inspections (FAI) and documenting results.</li><li>Proven experience with Non-Conformance Reports (NCRs) and nonconforming material processes.</li><li>Demonstrated capability in root cause analysis and Corrective and Preventive Action (CAPA) processes.</li></ul>Work EnvironmentThe role is based in a small manufacturing company environment with approximately 60 employees across production, engineering, quality, and front office support functions. The organization operates as a leading supplier to the aerospace industry, particularly in moisture control solutions. The standard schedule follows four 10-hour shifts per week, providing every Friday off. The work involves hands-on inspection activities in a regulated aerospace and defense manufacturing setting, using mechanical measurement tools, metrology equipment, CAD platforms, and potentially CMM systems. Team members collaborate closely across departments in a dynamic, quality-focused environment that supports continuous improvement and structured quality processes.Job Type &amp; LocationThis is a Permanent position based out of Princeton, NJ.Pay and BenefitsThe pay range for this position is $28.84 - $31.25/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 Princeton,NJ.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 Engineering Technicians NeededHelp Build the Future of Electric Vehicles!Join an innovative team at the forefront of EV manufacturing as a 2nd Shift Quality Technician (GA/Chassis/Battery). In this hands-on role, you'll be responsible for ensuring the quality, safety, and performance of cutting-edge electric vehicle systems. If you're passionate about quality, problem-solving, and making an impact in a fast-paced production environment, this is your opportunity to be part of a company transforming the future of transportation.Responsibilities<ul><li>Conduct quality inspections on vehicles to ensure compliance with standards.</li><li>Implement quality control measures to improve production processes.</li><li>Collaborate with cross-functional teams to enhance product reliability.</li><li>Maintain and calibrate test equipment.</li><li>Prepare test data and identify areas for quality control improvement.</li></ul>Essential Skills<ul><li>Troubleshooting and use of test equipment.</li><li>Experience in quality inspections, especially in the automotive or aerospace industry.</li><li>Proficiency in data analysis software.</li><li>Strong skills in Microsoft Office applications such as PowerPoint, Word, and Excel.</li><li>Experience in quality control, quality assurance, and electronics.</li><li>Ability to conduct root cause analysis.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience in quality control or assurance in a manufacturing environment, preferably in the automotive industry.</li><li>3+ years of experience in a related field.</li><li>Proficient in using inspection and testing equipment like calipers, micrometers, and multimeters.</li><li>Strong analytical and problem-solving skills.</li></ul>Work EnvironmentThe position will initially start on the 1st shift for 1-2 months, transitioning to the 2nd shift. Flexibility to work mandatory overtime and Saturdays is required. The role requires physical fitness and experience working on large vehicle structures.Job Type &amp; LocationThis is a Contract position based out of Garden Grove, CA.Pay and BenefitsThe pay range for this position is $25.00 - $32.00/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 Garden Grove,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: Senior Quality Engineering TechnicianJob DescriptionThe Senior Quality Engineering Technician leads inspection activities across incoming, in-process, and final inspection within a regulated aerospace and defense manufacturing environment. This role ensures strict compliance with AS9100 standards, customer specifications, and internal procedures while mentoring junior inspectors and supporting root cause investigation and corrective action implementation. The position plays a key role in maintaining product quality, driving continuous improvement, and upholding regulatory and customer requirements.Responsibilities<ul><li>Lead incoming, in-process, and final inspection activities for aerospace and defense components and assemblies.</li><li>Ensure all inspection work complies with AS9100 requirements, customer specifications, and internal quality procedures.</li><li>Read and interpret engineering drawings and blueprints, including GD&amp;T tolerancing, using CREO, CAD, and related tools.</li><li>Perform detailed mechanical inspections using calipers, gauges, micrometers, and other metrology equipment.</li><li>Conduct First Article Inspections (FAI) and document results in accordance with applicable standards and customer requirements.</li><li>Identify, document, and process nonconforming material, including generating Non-Conformance Reports (NCRs).</li><li>Support and lead root cause analysis activities for nonconformances and quality issues.</li><li>Participate in and support Corrective and Preventive Action (CAPA) processes to address quality problems and prevent recurrence.</li><li>Analyze GD&amp;T requirements to verify dimensional compliance and ensure proper interpretation of tolerances.</li><li>Collaborate with production, engineering, and quality teams to resolve quality issues and improve processes.</li><li>Mentor and guide junior inspectors, providing training and support on inspection techniques, tools, and quality procedures.</li><li>Utilize quality assurance and quality control best practices to maintain consistent inspection standards.</li><li>Support final inspection activities to verify that products meet all contractual, regulatory, and customer requirements prior to shipment.</li><li>Contribute to continuous improvement initiatives, including Six Sigma or Lean Manufacturing activities where applicable.</li><li>Maintain accurate inspection records, reports, and documentation in accordance with internal and external requirements.</li><li>Assist with or perform CMM inspections if experienced with CMM operation and programming.</li><li>Ensure adherence to applicable aerospace and defense regulations, including ITAR and DFARS, where required.</li></ul>Essential Skills<ul><li>5+ years of quality inspection experience in aerospace or defense manufacturing.</li><li>Strong knowledge of Geometric Dimensioning and Tolerancing (GD&amp;T) and blueprint reading.</li><li>Experience working in AS9100-regulated environments and familiarity with related standards such as AS9102.</li><li>Proficiency in mechanical inspection using calipers, gauges, micrometers, and other metrology tools.</li><li>Ability to read and interpret engineering drawings and blueprints in CREO, CAD, AutoCAD, and similar platforms.</li><li>Hands-on experience with incoming, in-process, and final inspection of parts and assemblies.</li><li>Experience performing First Article Inspections (FAI) and documenting results.</li><li>Proven experience with Non-Conformance Reports (NCRs) and nonconforming material processes.</li><li>Demonstrated capability in root cause analysis and Corrective and Preventive Action (CAPA) processes.</li><li>Background in quality assurance and quality control within a manufacturing environment.</li><li>Strong leadership skills with the ability to mentor and support junior inspectors.</li><li>Effective communication skills to collaborate with cross-functional teams and document findings clearly.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with Coordinate Measuring Machine (CMM) operation and programming.</li><li>Familiarity with ITAR and DFARS compliance requirements in aerospace and defense environments.</li><li>Background in Six Sigma or Lean Manufacturing methodologies.</li><li>Experience working as a Mechanical Inspector or Quality Control Inspector.</li><li>Exposure to GD&amp;T analysis and interpretation in complex mechanical assemblies.</li><li>Ability to interpret detailed blueprints and drawings for both simple and complex parts.</li><li>Experience with quality inspection in a highly regulated environment, including aerospace and defense.</li><li>Comfort working with quality inspection tools and software used for documentation and reporting.</li></ul>Work EnvironmentThe role is based in a small manufacturing company environment with approximately 60 employees across production, engineering, quality, and front office support functions. The organization operates as a leading supplier to the aerospace industry, particularly in moisture control solutions. The standard schedule follows four 10-hour shifts per week, providing every Friday off. The work involves hands-on inspection activities in a regulated aerospace and defense manufacturing setting, using mechanical measurement tools, metrology equipment, CAD platforms, and potentially CMM systems. Team members collaborate closely across departments in a dynamic, quality-focused environment that supports continuous improvement and structured quality processes.Job Type &amp; LocationThis is a Contract to Hire position based out of Cookstown, NJ.Pay and BenefitsThe pay range for this position is $28.84 - $31.25/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 Cookstown,NJ.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 Engineering Technicians NeededHelp Build the Future of Electric Vehicles!Join an innovative team at the forefront of EV manufacturing as a 2nd Shift Quality Technician (GA/Chassis/Battery). In this hands-on role, you'll be responsible for ensuring the quality, safety, and performance of cutting-edge electric vehicle systems. If you're passionate about quality, problem-solving, and making an impact in a fast-paced production environment, this is your opportunity to be part of a company transforming the future of transportation.Responsibilities<ul><li>Conduct quality inspections on vehicles to ensure compliance with standards.</li><li>Implement quality control measures to improve production processes.</li><li>Collaborate with cross-functional teams to enhance product reliability.</li><li>Maintain and calibrate test equipment.</li><li>Prepare test data and identify areas for quality control improvement.</li></ul>Essential Skills<ul><li>Troubleshooting and use of test equipment.</li><li>Experience in quality inspections, especially in the automotive or aerospace industry.</li><li>Proficiency in data analysis software.</li><li>Strong skills in Microsoft Office applications such as PowerPoint, Word, and Excel.</li><li>Experience in quality control, quality assurance, and electronics.</li><li>Ability to conduct root cause analysis.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience in quality control or assurance in a manufacturing environment, preferably in the automotive industry.</li><li>3+ years of experience in a related field.</li><li>Proficient in using inspection and testing equipment like calipers, micrometers, and multimeters.</li><li>Strong analytical and problem-solving skills.</li></ul>Work EnvironmentThe position will initially start on the 1st shift for 1-2 months, transitioning to the 2nd shift. Flexibility to work mandatory overtime and Saturdays is required. The role requires physical fitness and experience working on large vehicle structures.Job Type &amp; LocationThis is a Contract to Hire position based out of Garden Grove, CA.Pay and BenefitsThe pay range for this position is $25.00 - $32.00/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 Garden Grove,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: Senior Quality Engineering TechnicianJob DescriptionThe Senior Quality Engineering Technician leads inspection activities across incoming, in-process, and final inspection within a regulated aerospace and defense manufacturing environment. This role ensures strict compliance with AS9100 standards, customer specifications, and internal procedures while mentoring junior inspectors and supporting root cause investigation and corrective action implementation. The position plays a key role in maintaining product quality, driving continuous improvement, and upholding regulatory and customer requirements.Responsibilities<ul><li>Lead incoming, in-process, and final inspection activities for aerospace and defense components and assemblies.</li><li>Ensure all inspection work complies with AS9100 requirements, customer specifications, and internal quality procedures.</li><li>Read and interpret engineering drawings and blueprints, including GD&amp;T tolerancing, using CREO, CAD, and related tools.</li><li>Perform detailed mechanical inspections using calipers, gauges, micrometers, and other metrology equipment.</li><li>Conduct First Article Inspections (FAI) and document results in accordance with applicable standards and customer requirements.</li><li>Identify, document, and process nonconforming material, including generating Non-Conformance Reports (NCRs).</li><li>Support and lead root cause analysis activities for nonconformances and quality issues.</li><li>Participate in and support Corrective and Preventive Action (CAPA) processes to address quality problems and prevent recurrence.</li><li>Analyze GD&amp;T requirements to verify dimensional compliance and ensure proper interpretation of tolerances.</li><li>Collaborate with production, engineering, and quality teams to resolve quality issues and improve processes.</li><li>Mentor and guide junior inspectors, providing training and support on inspection techniques, tools, and quality procedures.</li><li>Utilize quality assurance and quality control best practices to maintain consistent inspection standards.</li><li>Support final inspection activities to verify that products meet all contractual, regulatory, and customer requirements prior to shipment.</li><li>Contribute to continuous improvement initiatives, including Six Sigma or Lean Manufacturing activities where applicable.</li><li>Maintain accurate inspection records, reports, and documentation in accordance with internal and external requirements.</li><li>Assist with or perform CMM inspections if experienced with CMM operation and programming.</li><li>Ensure adherence to applicable aerospace and defense regulations, including ITAR and DFARS, where required.</li></ul>Essential Skills<ul><li>5+ years of quality inspection experience in aerospace or defense manufacturing.</li><li>Strong knowledge of Geometric Dimensioning and Tolerancing (GD&amp;T) and blueprint reading.</li><li>Experience working in AS9100-regulated environments and familiarity with related standards such as AS9102.</li><li>Proficiency in mechanical inspection using calipers, gauges, micrometers, and other metrology tools.</li><li>Ability to read and interpret engineering drawings and blueprints in CREO, CAD, AutoCAD, and similar platforms.</li><li>Hands-on experience with incoming, in-process, and final inspection of parts and assemblies.</li><li>Experience performing First Article Inspections (FAI) and documenting results.</li><li>Proven experience with Non-Conformance Reports (NCRs) and nonconforming material processes.</li><li>Demonstrated capability in root cause analysis and Corrective and Preventive Action (CAPA) processes.</li><li>Background in quality assurance and quality control within a manufacturing environment.</li><li>Strong leadership skills with the ability to mentor and support junior inspectors.</li><li>Effective communication skills to collaborate with cross-functional teams and document findings clearly.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with Coordinate Measuring Machine (CMM) operation and programming.</li><li>Familiarity with ITAR and DFARS compliance requirements in aerospace and defense environments.</li><li>Background in Six Sigma or Lean Manufacturing methodologies.</li><li>Experience working as a Mechanical Inspector or Quality Control Inspector.</li><li>Exposure to GD&amp;T analysis and interpretation in complex mechanical assemblies.</li><li>Ability to interpret detailed blueprints and drawings for both simple and complex parts.</li><li>Experience with quality inspection in a highly regulated environment, including aerospace and defense.</li><li>Comfort working with quality inspection tools and software used for documentation and reporting.</li></ul>Work EnvironmentThe role is based in a small manufacturing company environment with approximately 60 employees across production, engineering, quality, and front office support functions. The organization operates as a leading supplier to the aerospace industry, particularly in moisture control solutions. The standard schedule follows four 10-hour shifts per week, providing every Friday off. The work involves hands-on inspection activities in a regulated aerospace and defense manufacturing setting, using mechanical measurement tools, metrology equipment, CAD platforms, and potentially CMM systems. Team members collaborate closely across departments in a dynamic, quality-focused environment that supports continuous improvement and structured quality processes.Job Type &amp; LocationThis is a Contract to Hire position based out of Cookstown, NJ.Pay and BenefitsThe pay range for this position is $28.84 - $31.25/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 Cookstown,NJ.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 Field TechnicianJob DescriptionThe Quality Field Technician supports on-shift quality coordination on the manufacturing production floor to ensure that all products meet established specifications and customer expectations. This role focuses on real-time analytical testing, quality issue resolution, and adherence to Good Manufacturing Practices while helping to establish and maintain basic quality systems for extended shelf life (ESL) dairy-related products. The Quality Field Technician works closely with Operations to monitor key quality attributes, support problem-solving, and maintain compliance with food safety and regulatory requirements.Responsibilities<ul><li>Achieve assigned goals related to production, safety, quality, performance, and cost.</li><li>Monitor the production floor and provide on-shift coordination, support, and focus for all quality-related issues.</li><li>Notify appropriate personnel of mechanical malfunctions to increase productivity and equipment capabilities, and identify opportunities where operators can assist in resolving concerns.</li><li>Comply with Good Manufacturing Practices (GMPs), Standard Operating Procedures (SOPs), and all plant policies, rules, and regulations.</li><li>Provide assistance and support to all areas related to quality as assigned by the supervisor or lead.</li><li>Ensure technicians maintain proper focus on all quality checks and provide follow-up training when needed.</li><li>Perform finished pallet audits, end-of-shift product reviews, and other quality checks to verify that quality standards are met.</li><li>Track packaging and processing Key Quality Attributes (KQAs), identify problem areas and trends, and respond to production operators’ quality questions and concerns.</li><li>Communicate effectively between shifts and with other departments, execute issue resolution, and escalate issues in a timely manner.</li><li>Communicate product disposition decisions and assist Operations with compliance to quality and specification standards.</li><li>Maintain accurate inventory of product in Quality Hold or retest status by performing routine cycle counts and reconciliations, and assist with cycle counts for reprocess and waste product.</li><li>Audit Operations paperwork for required departments to ensure timely completion and accuracy.</li><li>Participate in the Internal Quality Audit process to improve plant quality systems and GMP compliance.</li><li>Serve as a resource to Operations for auditing, updating, and documenting compliance with the Master Sanitation Schedule.</li><li>Conduct titration testing, verify chemical concentrations, and verify CIP (Clean-in-Place) dilution samples as needed.</li><li>Perform troubleshooting related to quality tests, results, or equipment as needed.</li><li>Perform finished product weight verifications and volumetric checks to confirm packaging accuracy.</li><li>Complete sensory analysis on finished products as required to assess product quality.</li><li>Conduct investigative research on products or materials as assigned by quality leadership.</li><li>Conduct ATP cleaning verification and line release processes per shift requirements.</li><li>Perform Environmental Swabbing as requested by Quality Assurance management.</li><li>Set up documentation and prepare sample shipments using proper shipping methods.</li><li>Cover breaks, lunches, and other staffing needs as assigned by the supervisor or lead.</li><li>Remain compliant with all legal requirements related to dairy processing and safety on the assigned shift and report any concerns to the supervisor or lead.</li><li>Work in a safe manner, promptly report safety concerns, and take corrective actions as necessary to maintain a safe environment.</li><li>Report food safety problems, initiate appropriate actions, and support SQF by maintaining food safety and food quality standards.</li><li>Ensure work areas remain sanitary and strictly adhere to sanitation practices.</li><li>Report to work at scheduled times and communicate tardiness or absences to the supervisor or manager prior to the occurrence.</li><li>Report to work in a condition fit to perform job duties.</li><li>Maintain a well-groomed appearance and dress in position-appropriate attire, including compliance with GMP dress code standards.</li><li>Comply with performance criteria and standards of conduct as outlined in company policies and procedures.</li></ul>Essential Skills<ul><li>Ability to apply basic to complex mathematical concepts, including addition, counting, subtraction, multiplication, division, and knowledge of weights and measures, to perform job tasks accurately.</li><li>Basic understanding of statistics and statistical process control, with strong attention to detail.</li><li>Ability to understand and respond appropriately to basic and complex inquiries from employees, vendors, and customers.</li><li>Ability to read, write, and communicate in English at a level sufficient to perform job functions.</li><li>Ability to operate quality and facility equipment required in the assigned area.</li><li>Ability to satisfactorily complete all required company training.</li><li>Ability to interpret company documents, literature, and UPC/code information.</li><li>Experience using Microsoft Windows and related software tools.</li><li>Minimum of a high school diploma or GED.</li><li>Manufacturing or machine operation experience, preferably 6 months to 2 years in the dairy or food industry (preferred but strongly beneficial).</li><li>Familiarity with SQF or similar quality systems (preferred).</li><li>Strong commitment to safety, food safety, and quality standards.</li><li>Effective communication skills to support cross-functional collaboration and shift-to-shift handoffs.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in chemistry, biology, food science, or agricultural technology science preferred.</li><li>Quality assurance, quality control, and quality inspection experience in a manufacturing environment.</li><li>Knowledge of chemistry and biology as applied to food or dairy processing.</li><li>Experience working with Good Manufacturing Practices (GMPs) and quality standards in a production environment.</li><li>Experience with quality systems such as SQF or similar frameworks.</li><li>Ability to learn and apply company mission, purpose, and goals and understand how the role contributes to achieving them.</li><li>Strong organizational skills to manage documentation, audits, and sample handling.</li><li>Ability to work independently and as part of a team in a fast-paced production environment.</li></ul>Work EnvironmentThis role is based on the manufacturing production floor in a dairy-related facility producing extended shelf life (ESL) products. The Quality Field Technician works on both day and night shifts, supporting continuous operations and interacting closely with production, sanitation, and quality teams. The environment involves working around production machinery, quality testing equipment, and sanitation systems such as CIP processes, as well as handling product samples for analytical, sensory, and microbiological-related verifications. The position requires strict adherence to Good Manufacturing Practices, sanitation standards, and food safety protocols. Team members are expected to maintain a safe work environment, promptly report and help correct safety concerns, and comply with all plant safety and quality procedures. Attire must be appropriate for a production and quality environment and must comply with GMP dress code standards, including any required protective clothing or equipment.Job Type &amp; LocationThis is a Contract to Hire position based out of Cortland, NY.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 Cortland,NY.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 Field Technician

Job Title: Quality Field TechnicianJob DescriptionThe Quality Field Technician supports on-shift quality coordination on the manufacturing production floor to ensure that all products meet established specifications and customer expectations. This role focuses on real-time analytical testing, quality issue resolution, and adherence to Good Manufacturing Practices while helping to establish and maintain basic quality systems for extended shelf life (ESL) dairy-related products. The Quality Field Technician works closely with Operations to monitor key quality attributes, support problem-solving, and maintain compliance with food safety and regulatory requirements.Responsibilities<ul><li>Achieve assigned goals related to production, safety, quality, performance, and cost.</li><li>Monitor the production floor and provide on-shift coordination, support, and focus for all quality-related issues.</li><li>Notify appropriate personnel of mechanical malfunctions to increase productivity and equipment capabilities, and identify opportunities where operators can assist in resolving concerns.</li><li>Comply with Good Manufacturing Practices (GMPs), Standard Operating Procedures (SOPs), and all plant policies, rules, and regulations.</li><li>Provide assistance and support to all areas related to quality as assigned by the supervisor or lead.</li><li>Ensure technicians maintain proper focus on all quality checks and provide follow-up training when needed.</li><li>Perform finished pallet audits, end-of-shift product reviews, and other quality checks to verify that quality standards are met.</li><li>Track packaging and processing Key Quality Attributes (KQAs), identify problem areas and trends, and respond to production operators’ quality questions and concerns.</li><li>Communicate effectively between shifts and with other departments, execute issue resolution, and escalate issues in a timely manner.</li><li>Communicate product disposition decisions and assist Operations with compliance to quality and specification standards.</li><li>Maintain accurate inventory of product in Quality Hold or retest status by performing routine cycle counts and reconciliations, and assist with cycle counts for reprocess and waste product.</li><li>Audit Operations paperwork for required departments to ensure timely completion and accuracy.</li><li>Participate in the Internal Quality Audit process to improve plant quality systems and GMP compliance.</li><li>Serve as a resource to Operations for auditing, updating, and documenting compliance with the Master Sanitation Schedule.</li><li>Conduct titration testing, verify chemical concentrations, and verify CIP (Clean-in-Place) dilution samples as needed.</li><li>Perform troubleshooting related to quality tests, results, or equipment as needed.</li><li>Perform finished product weight verifications and volumetric checks to confirm packaging accuracy.</li><li>Complete sensory analysis on finished products as required to assess product quality.</li><li>Conduct investigative research on products or materials as assigned by quality leadership.</li><li>Conduct ATP cleaning verification and line release processes per shift requirements.</li><li>Perform Environmental Swabbing as requested by Quality Assurance management.</li><li>Set up documentation and prepare sample shipments using proper shipping methods.</li><li>Cover breaks, lunches, and other staffing needs as assigned by the supervisor or lead.</li><li>Remain compliant with all legal requirements related to dairy processing and safety on the assigned shift and report any concerns to the supervisor or lead.</li><li>Work in a safe manner, promptly report safety concerns, and take corrective actions as necessary to maintain a safe environment.</li><li>Report food safety problems, initiate appropriate actions, and support SQF by maintaining food safety and food quality standards.</li><li>Ensure work areas remain sanitary and strictly adhere to sanitation practices.</li><li>Report to work at scheduled times and communicate tardiness or absences to the supervisor or manager prior to the occurrence.</li><li>Report to work in a condition fit to perform job duties.</li><li>Maintain a well-groomed appearance and dress in position-appropriate attire, including compliance with GMP dress code standards.</li><li>Comply with performance criteria and standards of conduct as outlined in company policies and procedures.</li></ul>Essential Skills<ul><li>Ability to apply basic to complex mathematical concepts, including addition, counting, subtraction, multiplication, division, and knowledge of weights and measures, to perform job tasks accurately.</li><li>Basic understanding of statistics and statistical process control, with strong attention to detail.</li><li>Ability to understand and respond appropriately to basic and complex inquiries from employees, vendors, and customers.</li><li>Ability to read, write, and communicate in English at a level sufficient to perform job functions.</li><li>Ability to operate quality and facility equipment required in the assigned area.</li><li>Ability to satisfactorily complete all required company training.</li><li>Ability to interpret company documents, literature, and UPC/code information.</li><li>Experience using Microsoft Windows and related software tools.</li><li>Minimum of a high school diploma or GED.</li><li>Manufacturing or machine operation experience, preferably 6 months to 2 years in the dairy or food industry (preferred but strongly beneficial).</li><li>Familiarity with SQF or similar quality systems (preferred).</li><li>Strong commitment to safety, food safety, and quality standards.</li><li>Effective communication skills to support cross-functional collaboration and shift-to-shift handoffs.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in chemistry, biology, food science, or agricultural technology science preferred.</li><li>Quality assurance, quality control, and quality inspection experience in a manufacturing environment.</li><li>Knowledge of chemistry and biology as applied to food or dairy processing.</li><li>Experience working with Good Manufacturing Practices (GMPs) and quality standards in a production environment.</li><li>Experience with quality systems such as SQF or similar frameworks.</li><li>Ability to learn and apply company mission, purpose, and goals and understand how the role contributes to achieving them.</li><li>Strong organizational skills to manage documentation, audits, and sample handling.</li><li>Ability to work independently and as part of a team in a fast-paced production environment.</li></ul>Work EnvironmentThis role is based on the manufacturing production floor in a dairy-related facility producing extended shelf life (ESL) products. The Quality Field Technician works on both day and night shifts, supporting continuous operations and interacting closely with production, sanitation, and quality teams. The environment involves working around production machinery, quality testing equipment, and sanitation systems such as CIP processes, as well as handling product samples for analytical, sensory, and microbiological-related verifications. The position requires strict adherence to Good Manufacturing Practices, sanitation standards, and food safety protocols. Team members are expected to maintain a safe work environment, promptly report and help correct safety concerns, and comply with all plant safety and quality procedures. Attire must be appropriate for a production and quality environment and must comply with GMP dress code standards, including any required protective clothing or equipment.Job Type &amp; LocationThis is a Contract to Hire position based out of Cortland, NY.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 Cortland,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.

Job Title: Quality InspectorJob DescriptionThis role focuses on performing accurate quality inspections for electro-mechanical and electronics-based products in a high-volume manufacturing environment. The Quality Inspector interprets engineering and manufacturing drawings, uses precision inspection tools to measure parts, and documents inspection results and non-conformities to support consistent product quality.Responsibilities<ul><li>Interpret manufacturing and engineering drawings, including reading drawing notes and understanding measurement requirements, to determine inspection criteria.</li><li>Perform incoming inspection of parts and materials to ensure they meet specifications before release to production.</li><li>Use precision inspection tools such as micrometers, calipers, and gages to measure parts and verify dimensional accuracy against blueprints.</li><li>Conduct visual inspections and use appropriate measuring tools to identify defects, non-conformities, and deviations from specifications.</li><li>Update and maintain inspection reports and quality documentation accurately and in a timely manner.</li><li>Document non-conformities clearly and completely to support corrective actions and continuous improvement.</li><li>Support quality control activities in an electronics and electro-mechanical manufacturing environment, including circuit board and PCBA inspection when applicable.</li><li>Assist in creating and performing First Article Inspection Reports (FAIRs) when required.</li><li>Contribute to quality documentation activities such as PPAPs, PFMEAs, and Control Plans when needed.</li><li>Collaborate with production, engineering, and quality teams to communicate inspection results and help resolve quality issues.</li></ul>Essential Skills<ul><li>At least 2 years of experience in quality inspection, gage calibration, or a quality technician role.</li><li>Proven ability to interpret manufacturing and engineering drawings, including schematics and blueprints.</li><li>Hands-on experience performing quality inspections using inspection tools such as micrometers, calipers, and gages.</li><li>Demonstrated ability to perform visual inspections and use measuring tools to verify parts against specifications.</li><li>Experience measuring parts and comparing results to blueprints and documented requirements.</li><li>Strong understanding of basic measurement principles and dimensional inspection.</li><li>Ability to update and maintain inspection reports and quality documentation accurately.</li><li>Experience in quality control or quality inspection within a manufacturing environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with electronics, including circuit board manufacturing, PCBA, or electro-mechanical manufacturing.</li><li>Exposure to or experience creating and performing First Article Inspection Reports (FAIRs).</li><li>Familiarity with PPAPs (Production Part Approval Process), PFMEA (Process Failure Mode and Effects Analysis), and Control Plans.</li><li>Experience working with quality documentation in a manufacturing setting.</li><li>Comfort working with schematics and technical documentation related to electro-mechanical systems.</li></ul>Work EnvironmentYou will work with precision inspection tools such as micrometers, calipers, and gages, and handle components related to circuit boards, PCBA, and electro-mechanical assemblies.Job Type &amp; LocationThis is a Contract to Hire position based out of Wheeling, IL.Pay and BenefitsThe pay range for this position is $23.00 - $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 Wheeling,IL.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 Inspector

Job Title: Quality InspectorJob DescriptionThe Quality Inspector supports aerospace precision manufacturing by performing dimensional inspections, maintaining accurate documentation, and managing nonconformances across incoming, in-process, and finished goods. This role ensures strict compliance with engineering specifications, AS9100 standards, and customer requirements while contributing to continuous improvement, root cause analysis, and corrective actions in a growing operation.Responsibilities<ul><li>Perform detailed dimensional inspections on incoming, in-process, and finished aerospace components to ensure they meet engineering drawings and specifications.</li><li>Operate coordinate measuring machines (CMM), with a strong focus on Zeiss systems, to verify complex geometries and critical features.</li><li>Interpret blueprints and apply GD&amp;T principles to accurately assess part conformance and identify deviations.</li><li>Use precision measurement tools, including calipers, micrometers, and gauges, to validate dimensions and tolerances.</li><li>Document inspection results accurately in ERP systems and maintain complete traceability records in accordance with AS9100 requirements.</li><li>Create and process nonconformance reports (NCRs) when parts do not meet specifications, ensuring issues are clearly described and properly recorded.</li><li>Support root cause analysis and corrective and preventive actions (CAPA) by providing detailed inspection data and participating in problem-solving activities.</li><li>Handle and move parts safely, including lifting items up to 50 lbs, and assist with occasional shipping and handling responsibilities.</li><li>Ensure all work complies with customer requirements, internal quality procedures, and aerospace/defense industry standards.</li><li>Contribute to continuous improvement efforts by identifying opportunities to enhance inspection processes, documentation accuracy, and overall product quality.</li><li>Collaborate with production, engineering, and quality teams on the manufacturing floor to resolve quality issues in a timely manner.</li><li>Maintain an organized, clean, and safe work area while following all required personal protective equipment (PPE) and safety practices.</li></ul>Essential Skills<ul><li>2–3+ years of quality inspection experience, with approximately 3 years preferred, particularly for weekend shifts.</li><li>Hands-on CMM operation experience (non-negotiable), with the ability to run programs and interpret results.</li><li>Proficiency in blueprint reading and geometric dimensioning and tolerancing (GD&amp;T) interpretation.</li><li>Experience using precision measurement tools such as calipers, micrometers, and gauges.</li><li>Ability to lift up to 50 lbs to support inspection and shipping/handling responsibilities.</li><li>Basic ERP skills and strong computer literacy for accurate documentation and data entry.</li><li>Experience working in an aerospace or AS9100-regulated quality environment.</li><li>Competence in inspection documentation, including nonconformance reports (NCRs), traceability records, and ERP-based quality records.</li><li>High school diploma or equivalent.</li></ul>Additional Skills &amp; Qualifications<ul><li>Zeiss CMM experience strongly preferred, with the ability to contribute as a plug-and-play operator.</li><li>Aerospace or defense manufacturing experience strongly preferred, including exposure to programs such as space or high-reliability applications.</li><li>Participation in root cause analysis and corrective and preventive action (CAPA) activities.</li><li>Technical training or coursework in manufacturing, metrology, or a related field.</li><li>Experience with documentation and traceability requirements typical of aerospace and defense environments.</li><li>Interest in working with high-impact aerospace and defense components and advanced inspection technologies.</li><li>Motivation to grow with a facility undergoing expansion and operational changes.</li></ul>Work EnvironmentThis role is based on a manufacturing floor environment that involves machining operations, metal components, and a consistent level of industrial noise. Personal protective equipment (PPE) is required, and team members work in close proximity to production and inspection equipment. The pace is fast and evolving due to an ongoing facility move and expansion, offering exposure to precision machining and advanced inspection technologies such as Zeiss CMMs and other precision measuring tools. The position includes a blend of inspection duties and occasional shipping and handling responsibilities, including lifting parts up to 50 lbs. Both weekday and weekend shifts are available, with weekend roles offering higher autonomy and a 7% shift differential. The work is hands-on and floor-based rather than a repetitive desk environment, providing opportunities to contribute directly to high-impact aerospace and defense components in a growing operation.Job Type &amp; LocationThis is a Contract to Hire position based out of Denver, CO.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Denver,CO.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 InspectorJob DescriptionThe Quality Inspector ensures that manufactured parts and assemblies meet all quality standards by performing first piece, in-process, and final inspections. This role sets up and uses a variety of gages and measuring equipment, conducts random audits at production machines, and collaborates closely with production teams to identify issues and implement effective solutions. The position requires at least 2 years of recent quality assurance experience in a manufacturing or machining environment, strong inspection skills, and the ability to work independently while contributing to a positive team environment.Responsibilities<ul><li>Perform first piece, in-process, and final inspections to verify that parts and assemblies meet specified requirements and quality standards.</li><li>Set up and use gages, including bore gages, gage blocks, rail gages, and other inspection tools, to accurately measure and validate product dimensions.</li><li>Identify and resolve minor inspection discrepancies during first piece and in-process inspections, and escalate major inspection issues to the Quality Engineer or Quality leadership as appropriate.</li><li>Conduct random inspection audits at production machines to monitor ongoing product quality and ensure adherence to specifications.</li><li>Work effectively with production employees to analyze quality issues, determine root causes, and implement practical corrective actions.</li><li>Promote and maintain a positive, collaborative team environment focused on continuous improvement and high-quality output.</li><li>Operate coordinate measuring machines (CMM) and other measuring devices such as micrometers, calipers, height stands, and comparators to perform precise dimensional checks.</li><li>Read and interpret engineering drawings, blueprints, and specifications to understand product requirements and inspection criteria.</li><li>Apply a general understanding of Geometric Dimensioning and Tolerancing (GD&amp;T) to evaluate part conformity and communicate findings.</li><li>Use Microsoft Office products to document inspection results, prepare reports, and maintain organized quality records.</li><li>Prioritize inspection tasks and manage workload effectively while working with minimal supervision.</li><li>Support calibration activities and proper use of inspection equipment to ensure accurate and reliable measurements.</li><li>Contribute to quality control and quality assurance initiatives within a machining and manufacturing environment, including metals and machine manufacturing operations.</li></ul>Essential Skills<ul><li>Minimum of 2 years of recent quality assurance or quality control experience, preferably in manufacturing or machining.</li><li>Proficiency in performing first piece, in-process, and final inspections.</li><li>Ability to set up and use a variety of gages, including bore gages, gage blocks, rail gages, and related inspection tools.</li><li>Experience with Zeiss Calypso software for CMM programming or operation.</li><li>Experience with Brown &amp; Sharpe MicroVal software for CMM programming or operation.</li><li>Strong ability to read and interpret engineering drawings, blueprints, and specifications.</li><li>General understanding of GD&amp;T application and interpretation in an inspection context.</li><li>Ability to operate coordinate measuring machines (CMM) and use micrometers, calipers, height stands, comparators, and other precision measuring devices.</li><li>Knowledge of manufacturing and machining processes, particularly in metals and machine manufacturing environments.</li><li>Proficiency with Microsoft Office products for documentation, reporting, and data tracking.</li><li>Good organizational skills with attention to detail and accuracy in inspection and recordkeeping.</li><li>Ability to prioritize tasks and work effectively with minimal supervision.</li><li>Strong quality inspection skills, including calibration awareness and quality checking of assemblies and components.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience performing quality control and quality assurance activities in a metals manufacturing environment.</li><li>Familiarity with inspection of assemblies and machine-manufactured components.</li><li>Comfort working with various calibration and measurement tools to maintain equipment reliability.</li><li>Strong communication skills to collaborate with production staff and convey inspection results clearly.</li><li>Demonstrated ability to contribute to a positive team environment and support continuous improvement efforts.</li></ul>Work EnvironmentThe role operates within a manufacturing and machining environment focused on metals and machine-produced components. Work is performed on or near production machinery and inspection areas, using coordinate measuring machines (CMM), micrometers, calipers, height stands, comparators, gage blocks, bore gages, rail gages, and other precision measuring devices. The position involves regular interaction with production employees and quality team members, with an emphasis on collaboration, problem solving, and maintaining high quality standards. The environment requires attention to safety, organization, and accuracy, and typically involves standard manufacturing hours with the need to manage multiple inspection priorities independently.Job Type &amp; LocationThis is a Contract to Hire position based out of South Milwaukee, WI.Pay and BenefitsThe pay range for this position is $25.00 - $33.00/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 South Milwaukee,WI.Application DeadlineThis position is anticipated to close on Aug 4, 2026.About Actalent 

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



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



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



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



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



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

Quality InspectorJob DescriptionJoin our dynamic team as a Quality Inspector Component and play a crucial role in ensuring the highest quality standards for our incoming components. This role offers a fantastic opportunity to grow within a rapidly expanding cosmetic manufacturing company.Responsibilities<ul><li>Inspect incoming components to ensure they meet quality standards.</li><li>Document and report any discrepancies or issues.</li><li>Collaborate with the quality control team to address and resolve any concerns.</li><li>Maintain accurate records of inspections and findings.</li></ul>Essential Skills<ul><li>Experience in first article inspection or a related field.</li><li>Strong attention to detail and analytical skills.</li><li>Excellent communication and documentation abilities.</li><li>Familiarity with industry standards and regulations.</li><li>Experience in non-conformance material report.</li></ul>Additional Skills &amp; Qualifications<ul><li>Proficiency in Microsoft Excel and Microsoft Office.</li><li>Knowledge of Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOP).</li><li>Understanding of quality inspection, quality control, and quality assurance principles.</li></ul>Work EnvironmentWork in a state-of-the-art manufacturing facility that includes a warehouse, lab, and production environment. The position follows a 1st shift schedule from Monday to Friday, with some Saturdays and overtime. Join a company experiencing significant growth and utilize advanced equipment to contribute to our success.Job Type &amp; LocationThis is a Contract to Hire position based out of Moorpark, CA.Pay and BenefitsThe pay range for this position is $22.00 - $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 Moorpark,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 Inspector Job DescriptionThe Quality Inspector supports daily operations by performing critical sampling, inspection, and basic testing of spices and seasonings in a production environment. This role ensures product integrity and quality by monitoring critical control points and verifying compliance with regulatory food safety standards, Good Manufacturing Practices (GMPs), and Good Laboratory Practices (GLPs). The Quality Inspector plays a vital role in identifying deviations, supporting corrective actions, and contributing to continuous improvement in quality manufacturing.Responsibilities<ul><li>Perform sampling and basic physical and organoleptic (sensory) testing of spices and seasonings in both laboratory and production environments.</li><li>Conduct seasoning and batch card reviews to verify accuracy and completeness of production documentation.</li><li>Ensure accurate label and weight verification of raw materials and finished product packaging on production lines.</li><li>Monitor and conduct checks of metal detection control points during production to ensure proper function and product safety.</li><li>Verify correct information and labeling of staged ingredients used in the production of seasoning formulations.</li><li>Ensure adherence to GMPs, GLPs, and all applicable food safety standards throughout daily activities.</li><li>Document and report all deviations and non-conformances to operations leads and quality control supervisors in a timely and accurate manner.</li><li>Maintain cleanliness and sanitation of the work environment, including laboratory and production areas.</li><li>Perform organoleptic sensory testing to evaluate product appearance, aroma, taste, and texture as required.</li><li>Carry out visual inspection and quality control checks on in-process and finished products.</li><li>Accurately enter quality data and test results into appropriate systems and records.</li><li>Support inspection and testing of incoming materials and ingredients as needed.</li><li>Assist with laboratory preparation, sample handling, and basic chemistry-related tasks as assigned.</li><li>Participate in inventory and sample management activities related to quality testing.</li><li>Collaborate with operations and quality teams to support corrective and preventive actions.</li><li>Perform other duties as requested in support of department and business needs.</li></ul>Essential Skills<ul><li>Experience in quality inspection, quality control, or quality assurance in a manufacturing or laboratory environment.</li><li>Ability to perform sample testing, including basic physical and organoleptic (sensory) evaluations.</li><li>Strong attention to detail with a focus on accuracy in documentation, labeling, and data entry.</li><li>Strong decision-making skills based on training and experience, with the ability to recognize and escalate quality issues.</li><li>Proactive approach with initiative to follow through on tasks to resolution.</li><li>Previous experience in a laboratory or food manufacturing environment (preferred).</li><li>Excellent verbal and written communication skills for clear reporting and collaboration.</li><li>Excellent interpersonal skills to work effectively with cross-functional teams.</li><li>Excellent time management skills with a proven ability to meet deadlines in a fast-paced environment.</li><li>Excellent organizational skills with the ability to handle multiple assignments simultaneously.</li><li>Proficiency with Microsoft Office Suite for documentation, reporting, and data management.</li><li>Comfort working with quality control inspection tools and processes, including visual inspection and metal detection checks.</li><li>Ability to maintain cleanliness and follow GMPs, GLPs, and food safety standards consistently.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree preferred, ideally in a scientific, food science, or related discipline.</li><li>Experience in a food manufacturing facility, particularly with spices or seasonings, is an advantage.</li><li>Familiarity with Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs).</li><li>Experience working in laboratory environments, including handling chemicals of varying hazards.</li><li>Comfort with organoleptic sensory testing, including evaluation of taste, smell, and appearance.</li><li>Background in basic chemistry, laboratory preparation, or sample receiving and management is beneficial.</li><li>Experience with data entry and maintaining quality records and documentation.</li><li>Ability to adapt to changing priorities and support multiple facilities or production lines as needed.</li></ul>Work EnvironmentThis role operates in both manufacturing and laboratory settings. The position involves moderate standing, walking, reaching, climbing, stacking, and lifting throughout the shift. The production environment can be loud and may have varying temperatures, ranging from hot to cold, and often carries strong spice odors and dust. The role also requires working in a laboratory setting with chemicals of varying hazards, following appropriate safety procedures and protocols. The Quality Inspector works around production equipment, metal detection systems, and packaging lines while adhering to Good Manufacturing Practices and sanitation standards. Attire typically includes appropriate personal protective equipment suitable for a food manufacturing and laboratory environment.Job Type &amp; LocationThis is a Contract to Hire position based out of Jessup, MD.Pay and BenefitsThe pay range for this position is $18.00 - $20.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality InspectorJob DescriptionThe Quality Inspector supports daily operations by performing critical sampling, inspection, and basic testing of spices and seasonings in a production environment. This role ensures product integrity and quality by monitoring critical control points and verifying compliance with regulatory food safety standards, Good Manufacturing Practices (GMPs), and Good Laboratory Practices (GLPs). The Quality Inspector plays a vital role in identifying deviations, supporting corrective actions, and contributing to continuous improvement in quality manufacturing.Responsibilities<ul><li>Perform sampling and basic physical and organoleptic (sensory) testing of spices and seasonings in both laboratory and production environments.</li><li>Conduct seasoning and batch card reviews to verify accuracy and completeness of production documentation.</li><li>Ensure accurate label and weight verification of raw materials and finished product packaging on production lines.</li><li>Monitor and conduct checks of metal detection control points during production to ensure proper function and product safety.</li><li>Verify correct information and labeling of staged ingredients used in the production of seasoning formulations.</li><li>Ensure adherence to GMPs, GLPs, and all applicable food safety standards throughout daily activities.</li><li>Document and report all deviations and non-conformances to operations leads and quality control supervisors in a timely and accurate manner.</li><li>Maintain cleanliness and sanitation of the work environment, including laboratory and production areas.</li><li>Perform organoleptic sensory testing to evaluate product appearance, aroma, taste, and texture as required.</li><li>Carry out visual inspection and quality control checks on in-process and finished products.</li><li>Accurately enter quality data and test results into appropriate systems and records.</li><li>Support inspection and testing of incoming materials and ingredients as needed.</li><li>Assist with laboratory preparation, sample handling, and basic chemistry-related tasks as assigned.</li><li>Participate in inventory and sample management activities related to quality testing.</li><li>Collaborate with operations and quality teams to support corrective and preventive actions.</li><li>Perform other duties as requested in support of department and business needs.</li></ul>Essential Skills<ul><li>Experience in quality inspection, quality control, or quality assurance in a manufacturing or laboratory environment.</li><li>Ability to perform sample testing, including basic physical and organoleptic (sensory) evaluations.</li><li>Strong attention to detail with a focus on accuracy in documentation, labeling, and data entry.</li><li>Strong decision-making skills based on training and experience, with the ability to recognize and escalate quality issues.</li><li>Proactive approach with initiative to follow through on tasks to resolution.</li><li>Previous experience in a laboratory or food manufacturing environment (preferred).</li><li>Excellent verbal and written communication skills for clear reporting and collaboration.</li><li>Excellent interpersonal skills to work effectively with cross-functional teams.</li><li>Excellent time management skills with a proven ability to meet deadlines in a fast-paced environment.</li><li>Excellent organizational skills with the ability to handle multiple assignments simultaneously.</li><li>Proficiency with Microsoft Office Suite for documentation, reporting, and data management.</li><li>Comfort working with quality control inspection tools and processes, including visual inspection and metal detection checks.</li><li>Ability to maintain cleanliness and follow GMPs, GLPs, and food safety standards consistently.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree preferred, ideally in a scientific, food science, or related discipline.</li><li>Experience in a food manufacturing facility, particularly with spices or seasonings, is an advantage.</li><li>Familiarity with Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs).</li><li>Experience working in laboratory environments, including handling chemicals of varying hazards.</li><li>Comfort with organoleptic sensory testing, including evaluation of taste, smell, and appearance.</li><li>Experience in basic chemistry, laboratory preparation, or sample receiving and management is beneficial.</li><li>Experience with data entry and maintaining quality records and documentation.</li><li>Ability to adapt to changing priorities and support multiple facilities or production lines as needed.</li></ul>Work EnvironmentThis role operates in both manufacturing and laboratory settings. The position involves moderate standing, walking, reaching, climbing, stacking, and lifting throughout the shift. The production environment can be loud and may have varying temperatures, ranging from hot to cold, and often carries strong spice odors and dust. The role also requires working in a laboratory setting with chemicals of varying hazards, following appropriate safety procedures and protocols. The Quality Inspector works around production equipment, metal detection systems, and packaging lines while adhering to Good Manufacturing Practices and sanitation standards. Attire typically includes appropriate personal protective equipment suitable for a food manufacturing and laboratory environment.Job Type &amp; LocationThis is a Contract to Hire position based out of Jessup, MD.Pay and BenefitsThe pay range for this position is $18.00 - $20.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality InvestigatorJob DescriptionThe Quality Investigator serves as an individual contributor within the QA Compliance department and works cross‑functionally across the plant to ensure that quality and compliance requirements are consistently maintained. This role leads and documents investigations, identifies root causes, recommends and tracks corrective and preventive actions, and supports audits and continuous improvement initiatives within an FDA‑regulated manufacturing environment.Responsibilities<ul><li>Investigate and complete site-related exceptions, including minor, major, and critical investigations, in alignment with departmental priorities and timelines.</li><li>Lead and perform Phase II out-of-specification (OOS) investigations, ensuring thorough, inspection-ready documentation that complies with GMP expectations.</li><li>Identify true root causes of deviations and non-conformances and recommend appropriate, sustainable corrective and preventive actions (CAPAs) to prevent recurrence.</li><li>Support external audits and inspections by regulatory agencies and customers, including activities such as document running, documentation pre-review, and acting as a scribe.</li><li>Assist the department in trending and analyzing quality metrics, including Cost of Poor Quality, Key Performance Indicators, Quality Management Reviews, and data trend analysis.</li><li>Support data compilation and documentation for site Annual Product Reviews (APRs) and other quality reports as required.</li><li>Participate as a team member in cross-functional problem-solving and brainstorming initiatives to drive continuous improvement across the site.</li><li>Revise, update, and create Standard Operating Procedures (SOPs) as needed to reflect current practices and regulatory expectations.</li><li>Prepare GEMBA plans and conduct GEMBA walks to drive compliance, enhance quality, and improve safety at the site.</li><li>Track the progress and performance of assigned investigations and tasks through to completion, and meet with management on a regular basis to report status and escalate issues as needed.</li><li>Make independent decisions and exercise sound personal judgment based on company policies, SOPs, and GMP requirements when executing investigations and quality activities.</li><li>Utilize SAP and other electronic systems to document investigations, track CAPAs, and manage quality records.</li><li>Work safely in accordance with applicable regulations, standards, and procedures, and act in a manner that minimizes risk to health and the environment.</li><li>Promptly notify management of unsafe conditions or practices, unlawful activities, or activities that present unreasonable health or environmental risk, and report all safety or environmental incidents immediately.</li><li>Support various information requests from corporate and other departments, and collaborate with corporate support groups to help drive global continuous improvement programs.</li><li>Perform other quality and compliance-related duties as assigned by management.</li></ul>Essential Skills<ul><li>Proven ability to lead minor, major, and critical quality investigations, including Phase II OOS investigations, using sound judgment and GMP principles.</li><li>Strong capability in root cause analysis, including the ability to identify true root causes and develop effective, sustainable CAPAs.</li><li>Deep working knowledge of FDA-regulated environments, including SOPs, cGMP requirements, and inspection expectations.</li><li>High proficiency in quality documentation, including investigation writing, metric trending, SOP revisions, and audit support, with strong attention to detail and data integrity.</li><li>Demonstrated ability to work effectively across Operations, Quality, Engineering, Supply Chain, and other functions to gather information, drive investigations, and close actions.</li><li>Minimum of 3–5 years of experience in a pharmaceutical, biological, or other FDA-regulated industry setting.</li><li>Good documentation practice skills and strong written and verbal communication skills to support investigations and cross-functional coordination.</li><li>Ability to work both as an individual contributor and as part of a team, with strong self-organization and follow-through.</li><li>Proficiency in SAP for quality and documentation-related activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry, Microbiology, Biology, Engineering, or another science-related discipline is preferred; relevant job experience may be considered in lieu of a degree.</li><li>Familiarity and skilled competency with computers and common business software.</li><li>Proficiency with MS Office applications, including Word, Excel, and Outlook.</li><li>Detail-oriented mindset with a strong focus on accuracy and data integrity.</li><li>Demonstrated ability to learn new skill sets and adapt to evolving processes and systems.</li></ul>Work EnvironmentThis is a first-shift position, Monday through Friday, typically from 8:00 a.m. to 4:30 p.m., based on-site at a manufacturing plant. The role primarily operates in an office setting within the plant and involves frequent use of computer systems for documentation, data analysis, and communication. The position requires periodic visits to laboratories, manufacturing areas, warehouses, and other plant locations, which may involve exposure to standard manufacturing noise and typical plant conditions. The role may require periodic gowning and entry into cleanroom-classified production areas in accordance with site procedures. Personal Protective Equipment (PPE) must be worn as required. The position requires the ability to lift, carry, push, or pull up to 40 pounds; frequent use of hands and fingers for typing, operating printers, and reviewing documentation; and the ability to sit, stand, and walk for extended periods. The role requires reliable on-site presence Monday through Friday and may occasionally require weekend work based on business needs.Job Type &amp; LocationThis is a Contract position based out of Raleigh, NC.Pay and BenefitsThe pay range for this position is $45.00 - $49.00/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 Raleigh,NC.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 Investigator

Job Title: Quality InvestigatorJob DescriptionThe Quality Investigator serves as an individual contributor within the QA Compliance department and works cross‑functionally across the plant to ensure that quality and compliance requirements are consistently maintained. This role leads and documents investigations, identifies root causes, recommends and tracks corrective and preventive actions, and supports audits and continuous improvement initiatives within an FDA‑regulated manufacturing environment.Responsibilities<ul><li>Investigate and complete site-related exceptions, including minor, major, and critical investigations, in alignment with departmental priorities and timelines.</li><li>Lead and perform Phase II out-of-specification (OOS) investigations, ensuring thorough, inspection-ready documentation that complies with GMP expectations.</li><li>Identify true root causes of deviations and non-conformances and recommend appropriate, sustainable corrective and preventive actions (CAPAs) to prevent recurrence.</li><li>Support external audits and inspections by regulatory agencies and customers, including activities such as document running, documentation pre-review, and acting as a scribe.</li><li>Assist the department in trending and analyzing quality metrics, including Cost of Poor Quality, Key Performance Indicators, Quality Management Reviews, and data trend analysis.</li><li>Support data compilation and documentation for site Annual Product Reviews (APRs) and other quality reports as required.</li><li>Participate as a team member in cross-functional problem-solving and brainstorming initiatives to drive continuous improvement across the site.</li><li>Revise, update, and create Standard Operating Procedures (SOPs) as needed to reflect current practices and regulatory expectations.</li><li>Prepare GEMBA plans and conduct GEMBA walks to drive compliance, enhance quality, and improve safety at the site.</li><li>Track the progress and performance of assigned investigations and tasks through to completion, and meet with management on a regular basis to report status and escalate issues as needed.</li><li>Make independent decisions and exercise sound personal judgment based on company policies, SOPs, and GMP requirements when executing investigations and quality activities.</li><li>Utilize SAP and other electronic systems to document investigations, track CAPAs, and manage quality records.</li><li>Work safely in accordance with applicable regulations, standards, and procedures, and act in a manner that minimizes risk to health and the environment.</li><li>Promptly notify management of unsafe conditions or practices, unlawful activities, or activities that present unreasonable health or environmental risk, and report all safety or environmental incidents immediately.</li><li>Support various information requests from corporate and other departments, and collaborate with corporate support groups to help drive global continuous improvement programs.</li><li>Perform other quality and compliance-related duties as assigned by management.</li></ul>Essential Skills<ul><li>Proven ability to lead minor, major, and critical quality investigations, including Phase II OOS investigations, using sound judgment and GMP principles.</li><li>Strong capability in root cause analysis, including the ability to identify true root causes and develop effective, sustainable CAPAs.</li><li>Deep working knowledge of FDA-regulated environments, including SOPs, cGMP requirements, and inspection expectations.</li><li>High proficiency in quality documentation, including investigation writing, metric trending, SOP revisions, and audit support, with strong attention to detail and data integrity.</li><li>Demonstrated ability to work effectively across Operations, Quality, Engineering, Supply Chain, and other functions to gather information, drive investigations, and close actions.</li><li>Minimum of 3–5 years of experience in a pharmaceutical, biological, or other FDA-regulated industry setting.</li><li>Good documentation practice skills and strong written and verbal communication skills to support investigations and cross-functional coordination.</li><li>Ability to work both as an individual contributor and as part of a team, with strong self-organization and follow-through.</li><li>Proficiency in SAP for quality and documentation-related activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry, Microbiology, Biology, Engineering, or another science-related discipline is preferred; relevant job experience may be considered in lieu of a degree.</li><li>Familiarity and skilled competency with computers and common business software.</li><li>Proficiency with MS Office applications, including Word, Excel, and Outlook.</li><li>Detail-oriented mindset with a strong focus on accuracy and data integrity.</li><li>Demonstrated ability to learn new skill sets and adapt to evolving processes and systems.</li></ul>Work EnvironmentThis is a first-shift position, Monday through Friday, typically from 8:00 a.m. to 4:30 p.m., based on-site at a manufacturing plant. The role primarily operates in an office setting within the plant and involves frequent use of computer systems for documentation, data analysis, and communication. The position requires periodic visits to laboratories, manufacturing areas, warehouses, and other plant locations, which may involve exposure to standard manufacturing noise and typical plant conditions. The role may require periodic gowning and entry into cleanroom-classified production areas in accordance with site procedures. Personal Protective Equipment (PPE) must be worn as required. The position requires the ability to lift, carry, push, or pull up to 40 pounds; frequent use of hands and fingers for typing, operating printers, and reviewing documentation; and the ability to sit, stand, and walk for extended periods. The role requires reliable on-site presence Monday through Friday and may occasionally require weekend work based on business needs.Job Type &amp; LocationThis is a Contract to Hire position based out of Raleigh, NC.Pay and BenefitsThe pay range for this position is $45.00 - $49.00/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 Raleigh,NC.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 InvestigatorJob DescriptionThe Quality Investigator serves as an individual contributor within the QA Compliance department and works cross‑functionally across the plant to ensure that quality and compliance requirements are consistently maintained. This role leads and documents investigations, identifies root causes, recommends and tracks corrective and preventive actions, and supports audits and continuous improvement initiatives within an FDA‑regulated manufacturing environment.Responsibilities<ul><li>Investigate and complete site-related exceptions, including minor, major, and critical investigations, in alignment with departmental priorities and timelines.</li><li>Lead and perform Phase II out-of-specification (OOS) investigations, ensuring thorough, inspection-ready documentation that complies with GMP expectations.</li><li>Identify true root causes of deviations and non-conformances and recommend appropriate, sustainable corrective and preventive actions (CAPAs) to prevent recurrence.</li><li>Support external audits and inspections by regulatory agencies and customers, including activities such as document running, documentation pre-review, and acting as a scribe.</li><li>Assist the department in trending and analyzing quality metrics, including Cost of Poor Quality, Key Performance Indicators, Quality Management Reviews, and data trend analysis.</li><li>Support data compilation and documentation for site Annual Product Reviews (APRs) and other quality reports as required.</li><li>Participate as a team member in cross-functional problem-solving and brainstorming initiatives to drive continuous improvement across the site.</li><li>Revise, update, and create Standard Operating Procedures (SOPs) as needed to reflect current practices and regulatory expectations.</li><li>Prepare GEMBA plans and conduct GEMBA walks to drive compliance, enhance quality, and improve safety at the site.</li><li>Track the progress and performance of assigned investigations and tasks through to completion, and meet with management on a regular basis to report status and escalate issues as needed.</li><li>Make independent decisions and exercise sound personal judgment based on company policies, SOPs, and GMP requirements when executing investigations and quality activities.</li><li>Utilize SAP and other electronic systems to document investigations, track CAPAs, and manage quality records.</li><li>Work safely in accordance with applicable regulations, standards, and procedures, and act in a manner that minimizes risk to health and the environment.</li><li>Promptly notify management of unsafe conditions or practices, unlawful activities, or activities that present unreasonable health or environmental risk, and report all safety or environmental incidents immediately.</li><li>Support various information requests from corporate and other departments, and collaborate with corporate support groups to help drive global continuous improvement programs.</li><li>Perform other quality and compliance-related duties as assigned by management.</li></ul>Essential Skills<ul><li>Proven ability to lead minor, major, and critical quality investigations, including Phase II OOS investigations, using sound judgment and GMP principles.</li><li>Strong capability in root cause analysis, including the ability to identify true root causes and develop effective, sustainable CAPAs.</li><li>Deep working knowledge of FDA-regulated environments, including SOPs, cGMP requirements, and inspection expectations.</li><li>High proficiency in quality documentation, including investigation writing, metric trending, SOP revisions, and audit support, with strong attention to detail and data integrity.</li><li>Demonstrated ability to work effectively across Operations, Quality, Engineering, Supply Chain, and other functions to gather information, drive investigations, and close actions.</li><li>Minimum of 3–5 years of experience in a pharmaceutical, biological, or other FDA-regulated industry setting.</li><li>Good documentation practice skills and strong written and verbal communication skills to support investigations and cross-functional coordination.</li><li>Ability to work both as an individual contributor and as part of a team, with strong self-organization and follow-through.</li><li>Proficiency in SAP for quality and documentation-related activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry, Microbiology, Biology, Engineering, or another science-related discipline is preferred; relevant job experience may be considered in lieu of a degree.</li><li>Familiarity and skilled competency with computers and common business software.</li><li>Proficiency with MS Office applications, including Word, Excel, and Outlook.</li><li>Detail-oriented mindset with a strong focus on accuracy and data integrity.</li><li>Demonstrated ability to learn new skill sets and adapt to evolving processes and systems.</li></ul>Work EnvironmentThis is a first-shift position, Monday through Friday, typically from 8:00 a.m. to 4:30 p.m., based on-site at a manufacturing plant. The role primarily operates in an office setting within the plant and involves frequent use of computer systems for documentation, data analysis, and communication. The position requires periodic visits to laboratories, manufacturing areas, warehouses, and other plant locations, which may involve exposure to standard manufacturing noise and typical plant conditions. The role may require periodic gowning and entry into cleanroom-classified production areas in accordance with site procedures. Personal Protective Equipment (PPE) must be worn as required. The position requires the ability to lift, carry, push, or pull up to 40 pounds; frequent use of hands and fingers for typing, operating printers, and reviewing documentation; and the ability to sit, stand, and walk for extended periods. The role requires reliable on-site presence Monday through Friday and may occasionally require weekend work based on business needs.Job Type &amp; LocationThis is a Contract position based out of Raleigh, NC.Pay and BenefitsThe pay range for this position is $45.00 - $49.00/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 Raleigh,NC.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: Quality InvestigatorJob DescriptionWe are seeking a dedicated Quality Investigator to join our QA Compliance department. As an individual contributor, you will work cross-functionally to maintain quality and compliance standards across the plant. This role is pivotal in ensuring the integrity of our processes and products.Responsibilities<ul><li>Investigate and complete site-related exceptions, including minor, major, and critical investigations, with coaching as needed.</li><li>Identify root causes and recommend appropriate Corrective and Preventive Actions (CAPAs) to address these causes.</li><li>Perform Phase II Out of Specification (OOS) investigations.</li><li>Support external audits from regulatory agencies and customers, including roles such as Document Runner, Documentation Pre-Review, and Scribe.</li><li>Assist in trending metrics such as Cost of Poor Quality, Key Performance Indicators, Quality Management Reviews, and Data Trend Analysis.</li><li>Compile data for site Annual Product Reviews (APRs).</li><li>Participate in brainstorming initiatives for continuous improvement.</li><li>Revise Standard Operating Procedures (SOPs) as needed.</li><li>Prepare GEMBA plans and conduct compliance and safety improvement walks.</li><li>Track and report the progress of assignments to management weekly.</li><li>Make independent decisions and exercise personal judgment based on company policies, SOPs, and Good Manufacturing Practices (GMPs).</li><li>Utilize SAP proficiently.</li><li>Perform other duties as assigned by management.</li></ul>Essential Skills<ul><li>Proficiency in deviation investigations, root cause analysis, and GMP compliance.</li><li>Proven ability to lead investigations, including Phase II OOS, using sound judgment and GMP principles.</li><li>Strong capability to identify true root causes and develop effective, sustainable CAPAs.</li><li>Deep working knowledge of FDA-regulated environments, SOPs, and cGMP requirements.</li><li>Ability to work effectively across Operations, Quality, Engineering, and Supply Chain.</li><li>High proficiency in investigation writing, metric trending, SOP revisions, and audit support with attention to detail and data integrity.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry, Microbiology, Biology, Engineering, or other science-related fields preferred.</li><li>3-5 years of experience in a pharmaceutical, biological, or other FDA-regulated industry setting.</li><li>Competency with computers and MS Office software (Word, Excel, and Outlook).</li><li>Good documentation practice skills.</li><li>Strong written and verbal communication skills.</li><li>Detail-oriented and self-organized.</li><li>Ability to work independently or as part of a team.</li><li>Demonstrated ability to learn new skill sets.</li></ul>Work EnvironmentThis position operates on the first shift, Monday through Friday, from 8am to 4:30pm. The role involves working in an office setting within a manufacturing plant, with visits to laboratories, manufacturing, warehouse, and other plant areas as needed. The position requires frequent use of computer systems and may involve periodic gowning and entry into cleanroom classified production areas. Exposure to standard manufacturing noise is possible. The role requires the ability to wear appropriate Personal Protective Equipment (PPE), lift up to 40 lbs, and involves frequent use of hands and fingers for typing and reviewing documentation. The ability to sit, stand, and walk for extended periods is required. Weekend work may be necessary if needed.Job Type &amp; LocationThis is a Contract position based out of Raleigh, NC.Pay and BenefitsThe pay range for this position is $45.00 - $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 fully onsite position in Raleigh,NC.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.

Description
					Shift 1 (8am-5pm) and 3rd - (11pm-7am) - only when certain products are produced

Baxter Bill Rate: $30.00

Job Responsibilities
• Perform chemical quantitative and qualitative analysis on intravenous solutions, sets, devices, raw materials, and plant water (distilled, non-distilled water) utilizing ‘wet’ chemistry techniques and instrument analysis
• Use laboratory instrumentation, computer systems and software to collect and record data
• Must be able to use standard software applications such as MS Office Suite
• Perform analysis requiring precise analytical skills and understanding of chemistry principles
• Perform investigations utilizing problem solving and troubleshooting
• Prepare and perform protocols
• Investigate deviations and ability to write exception documents
• Ensure regulatory compliance
• Learn, understand and apply rigorous quality standards, Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP).
• Complete and peer-review documentation
• Complete all testing, including special projects / protocol testing in a timely and appropriate manner
• Must perform all other duties and responsibilities as determined by supervision/management
• Must have knowledge of both plant and department environmental health and safety regulations and comply with said regulations accordingly
• Must be able to work off shift hours and some weekends
• Must notify the supervisor and take appropriate action if any safety, quality, mechanical or discrepancy issues occur
• Must sustain a clean and safe work area using 6S principles

Knowledge, Skill and Abilities
• Computer competency, required
• Ability to work independently
• Good organizational and time management skills
• Good oral and written communication skills.
• Ability to handle multiple priorities in a fast-paced environment

HPLC Experience Preferred

Physical Requirements
Candidate must not be color blind as determined by the Isihara’s Test for Color Deficiency
Candidates must meet near vision visual acuity requirements annually as documented in the Baxter-Cleveland Visual Acuity procedure CL-01-01-037

Required Education and Experience
• B.S. Degree in Science (Chemistry, Chemical Engineering, Physical Chemistry, Biology with Chemistry preferred)
• Quantitative analysis or equivalent lab experience
• Experience with instrumental analysis, required
• 2-4 Years experience

Other Duties as Assigned
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Overtime is worked as required.
										Skills
					Laboratory, Gmp, Chemistry, Biology, Hplc, Quality control, Analytical chemistry, Wet chemistry
										Top Skills Details
					Laboratory,Gmp,Chemistry,Biology,Hplc
										
					
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Contract position based out of Cleveland, MS.Pay and BenefitsThe pay range for this position is $18.75 - $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 Cleveland,MS.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

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



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



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



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



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



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

Quality Lab Associate I

Job Title: Quality Lab Technician – Raw Materials Job DescriptionThe Quality Lab Technician – Raw Materials plays a key role in ensuring that all incoming raw materials meet established quality standards before they enter production. This position focuses on inspecting, sampling, and testing materials, documenting findings, and collaborating closely with quality control and quality assurance teams to resolve issues and support continuous improvement in a fast-growing cosmetic manufacturing environment.Responsibilities<ul><li>Inspect incoming raw materials to verify they meet defined quality standards and specifications.</li><li>Perform sampling and first-article inspections on received materials in accordance with standard operating procedures (SOPs).</li><li>Conduct quality inspections using laboratory equipment such as pH meters and viscometers.</li><li>Process samples and compare results against Certificates of Analysis (COA) and internal criteria.</li><li>Document and report any discrepancies, defects, or non-conformances in raw materials.</li><li>Prepare and maintain Non-Conformance Material Reports (NCMR) and other quality documentation.</li><li>Collaborate with the quality control and quality assurance teams to address and resolve material-related concerns.</li><li>Maintain accurate and organized records of inspections, test results, and findings in Microsoft Excel and other Microsoft Office applications.</li><li>Follow Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and company SOPs at all times.</li><li>Support receiving inspection activities to ensure timely release or rejection of materials for production.</li><li>Participate in continuous improvement initiatives related to inspection processes and quality standards.</li><li>Ensure laboratory and production work areas remain clean, safe, and compliant with internal and regulatory requirements.</li></ul>Essential Skills<ul><li>Previous experience in raw material inspection or a closely related quality control or laboratory role.</li><li>Hands-on experience with sampling, receiving inspection, and first-article inspection of raw materials.</li><li>Strong attention to detail with the ability to identify and document discrepancies accurately.</li><li>Analytical skills to interpret test results and evaluate material conformity to specifications.</li><li>Proficiency with Microsoft Excel and familiarity with other Microsoft Office applications for documentation and reporting.</li><li>Experience processing samples and performing quality inspections using pH meters, viscometers, and other lab instruments.</li><li>Working knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).</li><li>Ability to follow and apply Standard Operating Procedures (SOPs) and quality standards consistently.</li><li>Experience preparing and managing Non-Conformance Material Reports (NCMR) and related quality documentation.</li><li>Effective written and verbal communication skills to collaborate with quality teams and production staff.</li><li>Ability to maintain accurate inspection records and quality documentation in a fast-paced environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with industry standards and regulations relevant to cosmetic or manufacturing environments.</li><li>Experience reviewing and verifying Certificates of Analysis (COA) from suppliers.</li><li>Background in quality control or quality assurance within a manufacturing or laboratory setting.</li><li>Understanding of general quality inspection principles and quality systems.</li><li>Ability to work cross-functionally with multiple departments in a growing organization.</li><li>Strong organizational skills and ability to manage multiple inspections and reports simultaneously.</li></ul>Work EnvironmentThis role operates within both laboratory and production environments in a state-of-the-art cosmetic manufacturing facility. The position is primarily on first shift, Monday through Friday, with some Saturdays and overtime as needed to support production demands. You will work with modern laboratory equipment, including pH meters and viscometers, and follow Good Manufacturing Practices, Good Laboratory Practices, and established SOPs. The environment emphasizes safety, cleanliness, and adherence to quality standards while providing opportunities to collaborate across departments and grow with a company experiencing significant expansion.Job Type &amp; LocationThis is a Contract position based out of Moorpark, CA.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/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 Moorpark,CA.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

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



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



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



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



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



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

Quality Lab Tech Raw Materials

Quality Lab techJob DescriptionThe Quality Lab Technician on 2nd shift supports quality control activities by processing samples, performing laboratory tests, and maintaining equipment and supplies in a state-of-the-art cosmetic manufacturing facility. This role ensures that raw materials and bulk products meet established quality standards by following Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP), and current Good Manufacturing Practices (cGMP). The technician works closely with laboratory and production teams to keep accurate records, uphold safety and housekeeping standards, and contribute to a growing organization.Responsibilities<ul><li>Assist in sample processing in accordance with Standard Operating Procedures (SOPs) and quality control requirements.</li><li>Issue and apply release stickers on approved raw materials and bulk products to indicate quality status.</li><li>Calibrate laboratory equipment, including instruments such as pH meters and viscometers, to ensure accurate test results.</li><li>Perform routine equipment maintenance and document activities as required.</li><li>Maintain inventory and ensure proper levels of laboratory and department supplies.</li><li>Order, unpack, log, and store laboratory supplies in an organized and traceable manner.</li><li>Assist in completing laboratory paperwork, documenting information accurately, completely, and in a timely manner.</li><li>Log, label, and process specimens and associated paperwork for testing according to established procedures.</li><li>Perform housekeeping and preventative maintenance of laboratory instruments to ensure reliable operation.</li><li>Ensure the laboratory area remains neat, clean, and organized at all times.</li><li>Maintain an ongoing awareness of cGMP, Good Laboratory Practices (GLP), good housekeeping standards, and safety requirements in the laboratory.</li><li>Collaborate with team members and supervisors to support production and quality objectives.</li><li>Follow verbal and written instructions accurately to complete assigned tasks.</li><li>Perform other duties as assigned to support overall laboratory and production operations.</li></ul>Essential Skills<ul><li>Ability to assist with sample processing in a quality control laboratory environment.</li><li>Hands-on experience or familiarity with pH meters and viscometers.</li><li>Working knowledge of Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP).</li><li>Proficiency with Microsoft Office applications, including Word, Excel, and Outlook.</li><li>Ability to accurately complete laboratory documentation and maintain detailed records.</li><li>Strong attention to detail and commitment to accuracy in testing and documentation.</li><li>Ability to prioritize tasks, multitask effectively, and manage time well in a fast-paced environment.</li><li>Excellent written and verbal communication skills.</li><li>Demonstrated reliability and punctuality.</li><li>Ability to work cooperatively with team members and supervisors.</li><li>Ability to understand and follow verbal and written directions.</li><li>High school diploma or GED.</li></ul>Additional Skills &amp; Qualifications<ul><li>BA or BS degree in Biological Science, Chemistry, or a combination of education and related experience.</li><li>Experience working in a laboratory environment is preferred.</li><li>Experience in the cosmetology or cosmetic manufacturing industry is preferred.</li><li>Knowledge of quality control principles and practices.</li><li>Comfort working with viscosity measurements and related testing.</li><li>Ability to adapt to changing priorities and support multiple departments as needed.</li></ul>Work EnvironmentThis role is based in a laboratory and production environment within a state-of-the-art cosmetic manufacturing facility that utilizes modern, state-of-the-art equipment. The position is scheduled on 2nd shift, with a typical shift starting at 12:00 p.m., and flexibility to work other shifts and Saturdays is desired to support production needs. The work involves regular interaction with laboratory instruments, sample handling, and movement between lab and production areas while maintaining high standards of cleanliness, organization, and safety.Job Type &amp; LocationThis is a Contract to Hire position based out of Moorpark, CA.Pay and BenefitsThe pay range for this position is $22.00 - $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 Moorpark,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.

Quality Lab Technician

Quality Lab Technician ($17/hr) - Lubbock, TX<h3>Overview</h3>Join one of the largest cotton seed operations in the world as a Quality Lab Technician. In this role, you’ll help ensure high-quality seed production by performing lab tests and inspections that support farmers across the U.S. and Mexico.Estimated Interview Date: July 24, 2026<h3>Key Responsibilities</h3><ul><li>Perform visual quality inspections on seed samples</li><li>Conduct lab testing (pH, moisture, protein assays, titrations)</li><li>Complete germination testing (warm &amp; cool)</li><li>Analyze seed purity and perform accurate seed counts</li><li>Collect and organize product samples</li></ul><h3>Requirements</h3><ul><li>High school diploma or GED</li><li>Degree in Agriculture, Plant Science, Natural Science, Chemistry, Biology or Science related field is a plus**</li><li>Experience in quality inspection, lab work, or agriculture preferred</li><li>Experience with seed testing, farm work, or manufacturing QC</li><li>Basic knowledge of biology, chemistry, or QC processes</li><li>Strong attention to detail and accuracy</li><li>Must provide Passport or Birth Certificate for onboarding</li></ul><h3>Schedule &amp; Environment</h3><ul><li>Standard: Mon–Fri, 7:00 AM – 5:30 PM</li><li>Peak season (Nov–Jan): Day &amp; night shifts available, up to 50 hrs/week</li><li>Feb–May: Weekend availability may be required</li><li>Fast-paced lab and production environment</li></ul>Job Type &amp; LocationThis is a Contract position based out of Lubbock, TX.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/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 Lubbock,TX.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 Lab Technician ($17/hr) - Lubbock, TX<h3>Overview</h3>Join one of the largest cotton seed operations in the world as a Quality Lab Technician. In this role, you’ll help ensure high-quality seed production by performing lab tests and inspections that support farmers across the U.S. and Mexico.Estimated Interview Date: July 30, 2026<h3></h3><h3>Key Responsibilities</h3><ul><li>Perform visual quality inspections on seed samples</li><li>Conduct lab testing (pH, moisture, protein assays, titrations)</li><li>Complete germination testing (warm &amp; cool)</li><li>Analyze seed purity and perform accurate seed counts</li><li>Collect and organize product samples</li></ul><h3>Requirements</h3><ul><li>High school diploma or GED</li><li>Degree in Agriculture, Plant Science, Natural Science, Chemistry, Biology or Science related field is a plus**</li><li>Experience in quality inspection, lab work, or agriculture preferred</li><li>Experience with seed testing, farm work, or manufacturing QC</li><li>Basic knowledge of biology, chemistry, or QC processes</li><li>Strong attention to detail and accuracy</li><li>Must provide Passport or Birth Certificate for onboarding</li></ul><h3>Schedule &amp; Environment</h3><ul><li>Standard: Mon–Fri, 7:00 AM – 5:30 PM</li><li>Peak season (Nov–Jan): Day &amp; night shifts available, up to 50 hrs/week</li><li>Feb–May: Weekend availability may be required</li><li>Fast-paced lab and production environment</li></ul>Job Type &amp; LocationThis is a Contract position based out of Lubbock, TX.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/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 Lubbock,TX.Application DeadlineThis position is anticipated to close on Aug 8, 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 Lab TechnicianJob DescriptionThe Quality Lab Technician is tasked with inspecting raw materials, in-process production, and finished goods to ensure they meet established quality standards and customer requirements. This role supports manufacturing operations by performing testing, documenting results, identifying quality concerns, and collaborating with production teams to drive continuous improvement. Safety, accuracy, and attention to detail are critical components of this position.Responsibilities<ul><li>Conduct quality testing on raw materials, work-in-process, and finished products.</li><li>Perform laboratory testing on raw materials and finished products.</li><li>Perform visual and dimensional inspections using standard measuring tools and equipment.</li><li>Verify product conformance to specifications and established quality requirements.</li><li>Collect product samples and perform routine testing procedures.</li><li>Record inspection and test results accurately and maintain quality documentation.</li><li>Assist in investigating product defects, nonconforming materials, and quality concerns.</li><li>Communicate quality issues to production leadership and manufacturing personnel.</li><li>Support incoming material inspections and supplier quality verification activities.</li><li>Participate in product evaluations and process audits.</li><li>Utilize computer systems to enter data, generate reports, and maintain records.</li><li>Follow established testing procedures, work instructions, and quality standards.</li><li>Maintain laboratory and inspection equipment in a clean and organized condition.</li><li>Assist with continuous improvement initiatives focused on quality, efficiency, and waste reduction.</li><li>Collaborate with production teams to improve product quality and reduce defects.</li><li>Train and support employees on quality procedures as needed.</li><li>Adhere to all safety policies, procedures, and personal protective equipment requirements.</li><li>Maintain a clean, safe, and organized work environment.</li><li>Perform additional duties as assigned.</li></ul>Essential Skills<ul><li>Quality control</li><li>Laboratory testing</li><li>Chemistry</li><li>Biology</li><li>Quality assurance</li><li>Titration</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma or equivalent required.</li><li>Degree in a technical life science discipline preferred.</li><li>Minimum one year of quality, laboratory, inspection, or manufacturing experience preferred.</li><li>Experience in a manufacturing environment is highly desired.</li></ul>Work EnvironmentThe work environment includes a bakery plant and laboratory setting. This role requires adherence to all safety protocols and the use of personal protective equipment. The environment is dynamic, supporting continuous improvement and growth, with a 50% chance of the position becoming permanent.Job Type &amp; LocationThis is a Contract position based out of Indianapolis, IN.Pay and BenefitsThe pay range for this position is $24.55 - $24.55/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 Indianapolis,IN.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.

<h1>🌱 Now Hiring: Laboratory Technicians – Seed Quality Testing</h1>Location: Lubbock, TXPay: $17/hrStart Date: August 2026Contract Opportunity with Potential for Long-Term EmploymentLooking for a hands-on role in agriculture and laboratory testing? Join a leading agricultural operation and help ensure the quality of seed products used by farmers across North America.<h3>What You'll Do</h3>✅ Perform visual inspections of seed samples✅ Conduct basic lab testing (pH, moisture, protein assays, titrations)✅ Complete germination and purity testing✅ Count, organize, and process samples✅ Follow laboratory procedures and accurately document results<h3>Qualifications</h3><ul><li>High School Diploma or GED required</li><li>Bachelor's degree in Agriculture, Plant Science, Natural Science, or related field preferred</li><li>Strong attention to detail and ability to follow procedures</li><li>Passport or Birth Certificate required for onboarding</li></ul><h3>Schedule</h3><ul><li>Regular Hours: Monday–Friday, 7:00 AM–5:30 PM</li><li>Peak Season (Nov–Jan): Must be open to 1st or 2nd shift, overtime, and weekend work</li><li>Up to 50 hours/week during busy seasons</li></ul><h3>Why Apply?</h3>🌾 Gain valuable laboratory and agricultural experience📈 Opportunity for long-term employment🩺 Medical, dental, and vision benefits available🤝 Join a team supporting the production of high-quality agricultural products<ul><li>Apply today to launch your career in laboratory science and agriculture! 🌱</li></ul>Job Type &amp; LocationThis is a Contract position based out of Lubbock, TX.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/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 Lubbock,TX.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 Lab Technician ($17/hr) - Lubbock, TX<h3>Overview</h3>Join one of the largest cotton seed operations in the world as a Quality Lab Technician. In this role, you’ll help ensure high-quality seed production by performing lab tests and inspections that support farmers across the U.S. and Mexico.Estimated Interview Date: July 24, 2026<h3>Key Responsibilities</h3><ul><li>Perform visual quality inspections on seed samples</li><li>Conduct lab testing (pH, moisture, protein assays, titrations)</li><li>Complete germination testing (warm &amp; cool)</li><li>Analyze seed purity and perform accurate seed counts</li><li>Collect and organize product samples</li></ul><h3>Requirements</h3><ul><li>High school diploma or GED</li><li>Degree in Agriculture, Plant Science, Natural Science, Chemistry, Biology or Science related field is a plus**</li><li>Experience in quality inspection, lab work, or agriculture preferred</li><li>Experience with seed testing, farm work, or manufacturing QC</li><li>Basic knowledge of biology, chemistry, or QC processes</li><li>Strong attention to detail and accuracy</li><li>Must provide Passport or Birth Certificate for onboarding</li></ul><h3>Schedule &amp; Environment</h3><ul><li>Standard: Mon–Fri, 7:00 AM – 5:30 PM</li><li>Peak season (Nov–Jan): Day &amp; night shifts available, up to 50 hrs/week</li><li>Feb–May: Weekend availability may be required</li><li>Fast-paced lab and production environment</li></ul>Job Type &amp; LocationThis is a Contract position based out of New Deal, TX.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/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 Deal,TX.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 Lab Technician ($17/hr) - Lubbock, TX<h3>Overview</h3>Join one of the largest cotton seed operations in the world as a Quality Lab Technician. In this role, you’ll help ensure high-quality seed production by performing lab tests and inspections that support farmers across the U.S. and Mexico.Estimated Interview Date: July 24, 2026<h3>Key Responsibilities</h3><ul><li>Perform visual quality inspections on seed samples</li><li>Conduct lab testing (pH, moisture, protein assays, titrations)</li><li>Complete germination testing (warm &amp; cool)</li><li>Analyze seed purity and perform accurate seed counts</li><li>Collect and organize product samples</li></ul><h3>Requirements</h3><ul><li>High school diploma or GED</li><li>Degree in Agriculture, Plant Science, Natural Science, Chemistry, Biology or Science related field is a plus**</li><li>Experience in quality inspection, lab work, or agriculture preferred</li><li>Experience with seed testing, farm work, or manufacturing QC</li><li>Basic knowledge of biology, chemistry, or QC processes</li><li>Strong attention to detail and accuracy</li><li>Must provide Passport or Birth Certificate for onboarding</li></ul><h3>Schedule &amp; Environment</h3><ul><li>Standard: Mon–Fri, 7:00 AM – 5:30 PM</li><li>Peak season (Nov–Jan): Day &amp; night shifts available, up to 50 hrs/week</li><li>Feb–May: Weekend availability may be required</li><li>Fast-paced lab and production environment</li></ul>Job Type &amp; LocationThis is a Contract position based out of Wolfforth, TX.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/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 Wolfforth,TX.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 Lab Technician – 2nd Shift Job DescriptionThe Quality Lab Technician on 2nd shift supports quality control activities by processing samples, performing laboratory tests, and maintaining equipment and supplies in a state-of-the-art cosmetic manufacturing facility. This role ensures that raw materials and bulk products meet established quality standards by following Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP), and current Good Manufacturing Practices (cGMP). The technician works closely with laboratory and production teams to keep accurate records, uphold safety and housekeeping standards, and contribute to a growing organization.Responsibilities<ul><li>Assist in sample processing in accordance with Standard Operating Procedures (SOPs) and quality control requirements.</li><li>Issue and apply release stickers on approved raw materials and bulk products to indicate quality status.</li><li>Calibrate laboratory equipment, including instruments such as pH meters and viscometers, to ensure accurate test results.</li><li>Perform routine equipment maintenance and document activities as required.</li><li>Maintain inventory and ensure proper levels of laboratory and department supplies.</li><li>Order, unpack, log, and store laboratory supplies in an organized and traceable manner.</li><li>Assist in completing laboratory paperwork, documenting information accurately, completely, and in a timely manner.</li><li>Log, label, and process specimens and associated paperwork for testing according to established procedures.</li><li>Perform housekeeping and preventative maintenance of laboratory instruments to ensure reliable operation.</li><li>Ensure the laboratory area remains neat, clean, and organized at all times.</li><li>Maintain an ongoing awareness of cGMP, Good Laboratory Practices (GLP), good housekeeping standards, and safety requirements in the laboratory.</li><li>Collaborate with team members and supervisors to support production and quality objectives.</li><li>Follow verbal and written instructions accurately to complete assigned tasks.</li><li>Perform other duties as assigned to support overall laboratory and production operations.</li></ul>Essential Skills<ul><li>Ability to assist with sample processing in a quality control laboratory environment.</li><li>Hands-on experience or familiarity with pH meters and viscometers.</li><li>Working knowledge of Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP).</li><li>Proficiency with Microsoft Office applications, including Word, Excel, and Outlook.</li><li>Ability to accurately complete laboratory documentation and maintain detailed records.</li><li>Strong attention to detail and commitment to accuracy in testing and documentation.</li><li>Ability to prioritize tasks, multitask effectively, and manage time well in a fast-paced environment.</li><li>Excellent written and verbal communication skills.</li><li>Demonstrated reliability and punctuality.</li><li>Ability to work cooperatively with team members and supervisors.</li><li>Ability to understand and follow verbal and written directions.</li><li>High school diploma or GED.</li></ul>Additional Skills &amp; Qualifications<ul><li>BA or BS degree in Biological Science, Chemistry, or a combination of education and related experience.</li><li>Experience working in a laboratory environment is preferred.</li><li>Experience in the cosmetology or cosmetic manufacturing industry is preferred.</li><li>Knowledge of quality control principles and practices.</li><li>Comfort working with viscosity measurements and related testing.</li><li>Ability to adapt to changing priorities and support multiple departments as needed.</li></ul>Work EnvironmentThis role is based in a laboratory and production environment within a state-of-the-art cosmetic manufacturing facility that utilizes modern, state-of-the-art equipment. The position is scheduled on 2nd shift, with a typical shift starting at 12:00 p.m., and flexibility to work other shifts and Saturdays is desired to support production needs. The work involves regular interaction with laboratory instruments, sample handling, and movement between lab and production areas while maintaining high standards of cleanliness, organization, and safety.Job Type &amp; LocationThis is a Contract to Hire position based out of Moorpark, CA.Pay and BenefitsThe pay range for this position is $22.00 - $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 Moorpark,CA.Application DeadlineThis position is anticipated to close on Jul 30, 2026.About Actalent 

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



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



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



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



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



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

Quality Lab Technician 2nd Shift

Job Title: Quality Line AuditorJob DescriptionThe Quality Line Auditor ensures that production lines consistently meet all requirements outlined in Batch Records, product specifications, and current Good Manufacturing Practices (cGMP). This role focuses on auditing production processes, inspecting manufacturing equipment for cleanliness, and driving corrective actions to maintain high-quality standards. The Quality Line Auditor also supports a culture of continuous improvement and lean practices while contributing to a diverse manufacturing environment that produces a wide range of consumer products.Responsibilities<ul><li>Audit production lines on time with a strong focus on detail to verify conformance to Batch Records, product specifications, and cGMP requirements.</li><li>Inspect manufacturing equipment for cleanliness and readiness prior to and during production.</li><li>Accurately record audit results in Batch Records and other required documentation.</li><li>Initiate corrective adjustments to manufacturing processes when needed, document all adjustments, and perform documented rechecks to verify that changes are effective.</li><li>Escalate issues according to established procedures to ensure timely correction and containment.</li><li>Immediately report non-conformances and quality concerns to the Quality Unit.</li><li>Support investigations of quality events as needed to identify root causes and help resolve issues.</li><li>Comply at all times with Standard Work, cGMP, Standard Operating Procedures (SOPs), and Work Instructions.</li><li>Understand, promote, and maintain a culture of lean action within the department, striving to continuously improve processes and eliminate waste.</li><li>Implement and maintain standards and processes that reduce or eliminate waste throughout the department.</li><li>Apply and utilize lean tools to implement permanent process improvements.</li><li>Institutionalize 5S (Sort, Straighten, Shine, Standardize, and Sustain) in all aspects of the department to maintain an organized and efficient work area.</li><li>Perform visual inspections and quality checks on products and processes as required.</li><li>Support internal audits and contribute to quality assurance and quality control activities.</li><li>Perform other work and related duties as assigned to support production and quality objectives.</li></ul>Essential Skills<ul><li>High School Diploma.</li><li>Prior auditing or inspection experience preferred, particularly in a production or manufacturing environment.</li><li>Prior exposure to quality assurance and quality control processes preferred.</li><li>Knowledge of quality assurance, quality control, and quality inspection practices.</li><li>Understanding of cGMP (current Good Manufacturing Practices) and SOP (Standard Operating Procedure) compliance.</li><li>Experience with inspection, quality checks, and visual inspection in a production setting.</li><li>Ability to read and write in English, including accurately completing Batch Records and quality documentation.</li><li>Strong verbal and written communication skills.</li><li>Effective multi-tasking skills with the ability to manage multiple audits or tasks in a dynamic environment.</li><li>Demonstrated sense of urgency and responsiveness to quality issues and production needs.</li><li>Critical thinking skills to identify non-conformances, evaluate root causes, and recommend corrective actions.</li><li>Strong organizational skills to manage documentation, audit schedules, and follow-up activities.</li><li>Ability to stand and walk frequently (4 to 6 hours per day).</li><li>Ability to perform infrequent to moderate bending, pushing, pulling, climbing stairs, reaching, lifting, and grasping.</li><li>Ability to perform infrequent to moderate repetitive motion and hand/wrist movement.</li><li>Ability to work at a computer terminal on an infrequent to moderate basis.</li><li>Good eyesight and normal hearing to effectively perform inspections and communicate in the work environment.</li><li>Fluency in the English language.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in a manufacturing or production environment with quality inspection responsibilities.</li><li>Background in internal auditing or participation in internal quality audits.</li><li>Familiarity with lean principles and tools used to drive continuous improvement and waste reduction.</li><li>Experience implementing or maintaining 5S practices (Sort, Straighten, Shine, Standardize, and Sustain).</li><li>Exposure to diverse consumer products such as beauty, bath and body, lip balms, skincare, sunscreens, and cleaning detergents.</li><li>Interest in long-term career growth, with the potential to move into roles such as QA Analyst or QA Specialist after 2–3 years of strong performance.</li><li>Ability to work effectively under tight deadlines and in a cyclical workflow environment with changing priorities.</li><li>Capability to handle moderate interruptions in workflow and adapt to starting and stopping tasks based on production and customer requirements.</li><li>Comfort with occasional work hours beyond the normal workday based on business demands.</li><li>Willingness and ability to move and lift objects, sometimes up to 50 lbs frequently.</li></ul>Work EnvironmentThis role is based at a manufacturing facility in Chaska and operates on a second shift schedule, typically from 2:00 PM to 10:00 PM, Monday through Friday, with a shift differential for second shift work. Depending on business needs and incoming components, 5–10 hours of overtime per week may be required, although the frequency and amount can vary. The position may require work hours beyond the normal workday and involves moderate to high demand for meeting tight deadlines. The work is cyclical in nature and includes moderate interruptions in workflow, with tasks starting and stopping based on production schedules and customer requirements. Travel is limited. The environment is indoors and can be seasonally cold, hot, or humid. Team members may be exposed to various fragrances, which at times may be present at elevated levels. The role involves frequent standing and walking for 4 to 6 hours per day, as well as infrequent to moderate bending, pushing, pulling, climbing stairs, reaching, lifting, grasping, and repetitive hand or wrist motion. Working at a computer terminal occurs on an infrequent to moderate basis. The facility supports a diverse manufacturing environment with exposure to a wide range of products, including beauty, bath and body, lip balms, skincare, sunscreens, cleaning detergents, and more. The organization is experiencing strong growth, with significant recent and projected expansion, creating opportunities for professional development and advancement over time.Job Type &amp; LocationThis is a Contract to Hire position based out of Chaska, MN.Pay and BenefitsThe pay range for this position is $21.00 - $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 Chaska,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.

Quality Line Auditor

Quality Manager needed in Midlothian, TXJob Duties:- Responsible for managing quality systems- Approves new and existing procedures that affect product and material quality- Collaborates with Regulatory Affairs- Oversees MOC, OOS, Deviation, and CAPA programs- Ensure efficiency and safety in the lab- Maintain SOP and other documentation on internal document management system- In charge of running customer audits as requested in a timely manner- Develops new programs to improve efficiency and work flowSchedule: Day ShiftPay: 130,000 - 145,000 USD Yearly depending in experienceAdditional Skills &amp; Qualifications- BS in Chemistry or a related field preferred- Internal Auditor Training- Experience with ISO 9001 and CGMP- 7+ years experience in CGMP environment in the Pharmaceutical manufacturing industry or Specialty Chemical Manufacturing- 3+ years of that experience in management/supervisor/lead role- Analytical chemistry lab experience- Experience with API's and Excipients required- Experience in both QC and QA funct- Relocation Available for candidates outside of Dallas/Fort WorthJob Type &amp; LocationThis is a Permanent position based out of Midlothian, TX.Pay and BenefitsThe pay range for this position is $130000.00 - $145000.00/yr.Not Applicable to this position.Workplace TypeThis is a fully onsite position in Midlothian,TX.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 Manager

Job Title: Quality ManagerJob DescriptionThis role leads and oversees the quality management system for assigned locations, ensuring compliance with standardized requirements and driving continuous improvement across all processes. The Quality Manager builds and guides a high-performing quality team, partners closely with internal and external stakeholders, and champions a culture of quality excellence within a dynamic manufacturing environment.Responsibilities<ul><li>Own and manage the quality management system for assigned locations to ensure full compliance with standardized requirements and industry best practices.</li><li>Lead, mentor, and develop a high-performing quality team, setting clear goals, providing coaching, and supporting professional growth.</li><li>Design, implement, and lead continuous improvement programs focused on enhancing product quality, process efficiency, and overall operational performance.</li><li>Plan, coordinate, and support internal and external quality audits, ensuring readiness, effective execution, and timely closure of findings.</li><li>Use root cause analysis methods to investigate quality issues, identify underlying causes, and implement sustainable corrective and preventive actions.</li><li>Collaborate closely with manufacturing, engineering, operations, and other functions to integrate quality standards into daily operations and new initiatives.</li><li>Establish, monitor, and report on quality metrics and key performance indicators to track performance and drive data-based decision making.</li><li>Make sound, timely decisions on quality-related matters, balancing customer requirements, operational constraints, and long-term business objectives.</li><li>Build and maintain strong relationships with customers, suppliers, and internal stakeholders to promote trust, transparency, and alignment on quality expectations.</li><li>Promote a continuous improvement mindset across the organization by sharing best practices, facilitating problem-solving sessions, and encouraging employee involvement in quality initiatives.</li></ul>Essential Skills<ul><li>Comprehensive knowledge of quality management systems and their application within manufacturing environments.</li><li>Proven experience leading and maintaining quality management systems compliant with standardized requirements.</li><li>Strong decision-making skills with the ability to evaluate complex information and act decisively on quality issues.</li><li>Advanced problem-solving abilities, including the use of structured root cause analysis techniques.</li><li>Demonstrated continuous improvement mindset with experience implementing and sustaining improvement initiatives.</li><li>Ability to build and maintain trust with internal and external stakeholders through clear communication and follow-through.</li><li>Minimum of seven years of experience in quality or a closely related field.</li><li>Manufacturing experience with hands-on exposure to production environments.</li><li>Demonstrated success in leadership roles, including leading teams and driving departmental objectives.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in engineering, operations, quality, or a related field, or an equivalent combination of education and experience.</li><li>ASQ Certification preferred, reflecting formal training and recognition in quality disciplines.</li><li>Experience working in a machine shop or similar manufacturing setting with customized or specialized work.</li><li>Strong interpersonal and communication skills, with the ability to influence and collaborate across functions.</li><li>Comfort working in a mid-sized organization where responsibilities are broad and workdays are varied and unique.</li></ul>Work EnvironmentThis role operates within a machine shop environment characterized by a mid-sized operation and customized work that brings variety and uniqueness to each workday. The setting involves close collaboration with production, engineering, and operations teams on the shop floor and in office areas. The work environment emphasizes hands-on engagement with manufacturing processes, practical problem solving, and continuous improvement activities in a production-focused facility.Job Type &amp; LocationThis is a Permanent position based out of Bedford, PA.Pay and BenefitsThe pay range for this position is $75000.00 - $100000.00/yr.HIGHLIGHTS OF YOUR BENEFITS

 Anthem BC/BS Medical PPO and Prescription Drug plan Delta Dental PPO plan VSP Vision plan Employer-paid Basic Life insurance and Accidental Death &amp; Dismemberment (AD&amp;D) Voluntary Life/AD&amp;D insurance Salary Continuation/Employer-paid Long Term Disability Health Reimbursement Account (HRA) Flexible Spending Account (FSA) with Employee Benefits Corporation Dependent Care FSA Voluntary Accident, Voluntary Critical Illness Voluntary Spousal/Dependent Life Insurance and AD&amp;DWorkplace TypeThis is a fully onsite position in Bedford,PA.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.

Quality &amp; Food Safety Supervisor<h3>Position Summary</h3>We are seeking a Quality &amp; Food Safety Supervisor to support USP compliance, laboratory operations, quality systems, and regulatory requirements within a manufacturing environment. This role serves as a backup to site Quality leadership and helps ensure product safety, quality, integrity, and compliance with USP and FDA regulations.<h3>Key Responsibilities</h3><ul><li>Ensure compliance with USP standards, GMPs, and regulatory requirements.</li><li>Support customer complaint investigations, root cause analysis, and corrective actions.</li><li>Assist with regulatory and customer audits.</li><li>Oversee USP laboratory testing, product release, and GLP programs.</li><li>Review and maintain SOPs, COAs, quality records, and compliance documentation.</li><li>Coordinate USP testing schedules and validation studies.</li><li>Monitor quality trends and support reporting requirements.</li><li>Supervise and schedule USP laboratory personnel.</li><li>Support training programs and promote a strong quality culture.</li><li>Manage laboratory supplies and equipment needs.</li></ul><h3>Qualifications</h3><ul><li>Bachelor’s degree in Chemistry, Biology, Food Science, or related scientific field.</li><li>2+ years of experience in a USP-regulated pharmaceutical manufacturing or quality laboratory environment.</li><li>Knowledge of 21 CFR 210, 21 CFR 211, ICH Q7, and related GMP regulations.</li><li>Strong problem-solving, communication, and organizational skills.</li><li>Ability to work effectively in a fast-paced manufacturing environment.</li><li>Supervisory experience preferred.</li></ul><h3>Preferred Skills</h3><ul><li>Experience with audits, validation programs, CAPA investigations, and quality systems.</li><li>Ability to lead cross-functional initiatives and drive continuous improvement.</li><li>Strong attention to detail and commitment to compliance and product quality.</li></ul>Apply today! Only one spot remaining!Job Type &amp; LocationThis is a Permanent position based out of Grand Saline, TX.Pay and BenefitsThe pay range for this position is $75000.00 - $100000.00/yr.401k Vision Dental BenefitsWorkplace TypeThis is a fully onsite position in Grand Saline,TX.Application DeadlineThis position is anticipated to close on Aug 7, 2026.About Actalent 

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



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



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



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



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



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

Job Title: Quality ManagerJob DescriptionThe Quality Manager is responsible for establishing, maintaining, and improving quality systems to ensure product and component compliance. This role oversees inspection processes, supplier quality, and continuous improvement initiatives while ensuring adherence to ISO 9001 and BRC standards.Responsibilities<ul><li>Establish inspection processes for manufactured and purchased products.</li><li>Define in-process and final inspection requirements.</li><li>Maintain statistical quality data and analyze for process improvements.</li><li>Conduct internal audits for compliance with quality plans.</li><li>Investigate customer complaints and implement corrective actions.</li><li>Manage returned goods and determine disposition.</li><li>Establish vendor quality standards and evaluate supplier performance.</li><li>Train personnel on quality procedures and ensure consistency.</li><li>Evaluate new products, processes, and equipment for quality impact.</li><li>Disposition non-conforming materials.</li><li>Ensure compliance with ISO 9001 and BRC standards.</li><li>Implement preventive actions to reduce defects.</li><li>Perform other duties as required.</li></ul>Essential Skills<ul><li>Problem Solving: Analyze quality data and implement corrective actions.</li><li>Technical Expertise: Deep understanding of ISO systems and inspection methods.</li><li>Communication: Collaborate across departments and suppliers.</li><li>Leadership: Guide teams in maintaining quality standards.</li><li>Attention to Detail: Ensure accuracy in inspections and reporting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Degree from an accredited college or institution.</li><li>7+ years of quality experience.</li><li>Vast knowledge of ISO certification and processes.</li><li>Experience with inspection tools, internal audits, injection mold, gauge, and tight tolerances.</li><li>Familiarity with PPAP, CAPA, and non-conforming materials.</li></ul>Work EnvironmentEmployees work in clean, well-lit, and ventilated environments. The role requires stamina due to standing and light-to-moderate lifting throughout the shift. Work is performed near high-speed machines, and safety equipment is required.Job Type &amp; LocationThis is a Permanent position based out of Racine, WI.Pay and BenefitsThe pay range for this position is $80000.00 - $90000.00/yr.Health
Dental
Vision
401kWorkplace TypeThis is a fully onsite position in Racine,WI.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: Quality Manager – Medical TechnologiesJob DescriptionThe Quality Manager for Medical Technologies plays a critical role in ensuring quality and regulatory compliance across the entire product lifecycle, from initial design and supplier materials to manufacturing processes and finished medical devices. This role maintains and enhances the Quality Management System (QMS) in alignment with FDA 21 CFR Part 820 and other applicable medical technology regulations, while driving continuous improvement initiatives. The Quality Manager manages supplier quality performance, supports design transfer, and contributes to post-market surveillance to ensure the safety, efficacy, and reliability of innovative medical technologies within a dynamic startup environment.Responsibilities<ul><li>Serve as the company’s Quality Management Representative and act as the primary point of contact for quality-related matters.</li><li>Collect, analyze, and report relevant quality key performance indicators (KPIs) and lead management review meetings to drive data-based decision-making.</li><li>Ensure continued compliance of the Quality Management System (QMS) with FDA 21 CFR Part 820 (Quality System Regulation) and other applicable international medical technology regulations.</li><li>Develop, implement, and maintain quality procedures, work instructions, and documentation related to operations and supplier quality.</li><li>Plan, conduct, and document internal audits to verify QMS effectiveness and identify opportunities for improvement.</li><li>Support and participate in external audits, including supplier audits and customer audits, ensuring timely response to findings and corrective actions.</li><li>Actively participate in risk management activities throughout the product lifecycle, including hazard analyses and design and process risk assessments.</li><li>Ensure identified risks are effectively mitigated and controlled within operations and throughout the supply chain.</li><li>Monitor and control manufacturing processes to ensure product quality, consistency, and compliance with design specifications and regulatory requirements.</li><li>Lead and participate in Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) investigations for manufacturing nonconformances, deviations, and customer complaints.</li><li>Support, review, and approve process validation activities (IQ, OQ, PQ) for new and existing manufacturing equipment and processes.</li><li>Implement and maintain Statistical Process Control (SPC) techniques to monitor and manage critical process parameters.</li><li>Drive continuous improvement projects within manufacturing operations using Lean, Six Sigma, and other quality methodologies.</li><li>Review and approve manufacturing batch records and Device History Records (DHRs) to support product release decisions.</li><li>Collaborate closely with cross-functional teams, including design, operations, and supply chain, to ensure robust design transfer and ongoing product quality.</li><li>Manage supplier quality performance, including qualification, auditing, and ongoing oversight, to ensure consistent delivery of compliant materials and components.</li><li>Communicate effectively with internal stakeholders and external parties such as suppliers and auditors to align on quality expectations and outcomes.</li><li>Contribute to a culture of quality and continuous improvement within a fast-paced medical technology startup environment.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Engineering (such as Biomedical, Mechanical, Electrical, or Industrial), Quality Management, or a related technical field.</li><li>5–7 years of progressive experience in quality engineering, quality assurance, and/or related quality roles within the medical or regulated manufacturing industry.</li><li>In-depth knowledge and hands-on experience with FDA 21 CFR Part 820 (Quality System Regulation).</li><li>Experience working within regulated medical technology or medical device manufacturing environments and understanding of applicable international regulations.</li><li>Experience with risk management activities and standards in a medical technology context, including conducting hazard analyses and risk assessments.</li><li>Demonstrated experience with medical technology manufacturing processes and process controls.</li><li>Proficiency with quality tools and methodologies such as Root Cause Analysis (RCA), Corrective and Preventive Action (CAPA), Failure Modes and Effects Analysis (FMEA), Control Plans, Statistical Process Control (SPC), Gauge R&amp;R, and Design of Experiments (DOE).</li><li>Experience with supplier qualification, auditing, and ongoing supplier management in a regulated environment.</li><li>Strong analytical, problem-solving, and critical thinking skills applied to complex quality and manufacturing challenges.</li><li>Excellent written and verbal communication skills, with the ability to interact effectively with all levels of the organization and external stakeholders including suppliers and auditors.</li><li>Ability to work both independently and collaboratively in a dynamic, fast-paced medical technology environment.</li><li>Proficiency in Microsoft Office Suite, including Excel, Word, and PowerPoint.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with ERP systems to support manufacturing, quality, and supply chain processes.</li><li>Experience using electronic Quality Management System (eQMS) software.</li><li>Certified Quality Engineer (CQE) or similar professional quality certification.</li><li>Lean Six Sigma training or certification, including Green Belt or Black Belt credentials.</li><li>Prior experience in a startup or early-stage medical technology environment.</li><li>Demonstrated ability to lead cross-functional continuous improvement initiatives.</li><li>Interest in working with cutting-edge medical technologies such as electromagnetic tracking platforms.</li></ul>Work EnvironmentThe role is based in a growing medical technology startup environment located within a multi-room facility in the UEL building in St. Paul, Minnesota. The site currently consists of four rooms, including dedicated office space for administrative and engineering work, an assembly area for hands-on manufacturing and product build activities, and shelf space for storing and staging final products. The current team is approximately eight people, offering close collaboration with experienced colleagues and the opportunity to shape processes and culture as the organization expands. As the company grows, there is potential to build out the existing space further and eventually move to a larger location. The environment is dynamic, fast-paced, and innovation-focused, providing exposure to advanced medical technology development and the full product lifecycle.Job Type &amp; LocationThis is a Permanent position based out of Saint Paul, MN.Pay and BenefitsThe pay range for this position is $120000.00 - $140000.00/yr.Healthcare: Comprehensive health, dental, and vision insurance with Flexible Spending Accounts (FSA) and mental health coverage. Financial &amp; Retirement: 401(k) retirement plan, Employee Stock Purchase Plan (ESPP), and company equity opportunities. Work-Life &amp; Family: Generous parental leave and paid time off. Additional Perks: Emotional wellness programs and, depending on the office location, social events and on-site perks.Workplace TypeThis is a fully onsite position in Saint Paul,MN.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.

On Site Quality Manager needed in Midlothian, TXJob Duties:- Responsible for managing quality systems- Approves new and existing procedures that affect product and material quality- Collaborates with Regulatory Affairs- Oversees MOC, OOS, Deviation, and CAPA programs- Ensure efficiency and safety in the lab- Maintain SOP and other documentation on internal document management system- In charge of running customer audits as requested in a timely manner- Develops new programs to improve efficiency and work flowSchedule: Day ShiftPay: 130,000 - 145,000 USD Yearly depending in experienceAdditional Skills &amp; Qualifications- BS in Chemistry or a related field preferred- Internal Auditor Training- Experience with ISO 9001 and CGMP- 7+ years experience in CGMP environment in the Pharmaceutical manufacturing industry or Specialty Chemical Manufacturing- 3+ years of that experience in management/supervisor/lead role- Analytical chemistry lab experience- Experience with API's and Excipients required- Experience in both QC and QA functionsJob Type &amp; LocationThis is a Permanent position based out of Midlothian, TX.Pay and BenefitsThe pay range for this position is $130000.00 - $145000.00/yr.Not Applicable to this position.Workplace TypeThis is a fully onsite position in Midlothian,TX.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.

Description The Quality Manager is responsible for overseeing and maintaining the quality assurance (QA) and quality control (QC) programs in a 503B outsourcing facility. This role ensures compliance with FDA, cGMP (Current Good Manufacturing Practices), USP &lt;797&gt;, USP &lt;800&gt;, and DEA regulations. The Quality Manager will lead audits, manage investigations, and drive continuous improvement initiatives to uphold product safety, efficacy, and sterility Job Activities and Responsibilities:Ensure compliance with FDA 21 CFR Part 210 &amp; 211, USP &lt;797&gt;, USP &lt;800&gt;, and cGMP requirements.Demonstrate proficiency and follow Standard Operating Procedures related to sterile compounding, cleanroom operations and quality control.Develop and implement quality assurance procedures to ensure the quality of compounded medication, including but not limited to the materials, storage, preparation, and dispensing of compounded medication.Supervise environmental monitoring (EM), sterility, endotoxin, and particulate testing to ensure product safetyCoordinate internal audits, supplier audits, and regulatory inspections, responding to findings with appropriate action plansOversee QA/QC functions performed by compounding and quality personnel to ensure that procedures are followed and that all QA/QC tasks are properly documented.Work directly with Departmental Managers to assist with personnel training and compounding validations, including but not limited to scheduling, completing, and documenting all initial and ongoing Aseptic Process Simulations (APS), personnel skill assessments, didactic evaluations, and training plans.Oversee quality risk management, deviation investigations, CAPAs (Corrective and Preventive Actions), and change controlsWork with Department Managers to evaluate patient complaints and adverse events, ensuring appropriate investigations and resolution.Oversees and maintains facility and equipment requirements, including but not limited to annual and biannual room certifications, monthly audits, equipment certifications, calibrations, and maintenance, and coordinates scheduling with Departmental Managers.Ensure proper validation of equipment, processes, and analytical methods used in production.Directly responsible for communication, documentation, and follow up with third-party laboratories regarding product testing, environmental sampling, and ongoing quality and stability study projects.Review and approve batch records, certificates of analysis (COAs), and release specificationsAssist Departmental Managers with recalls of medications when applicable.Assist General Manager/Operations Manager with board of pharmacy, FDA, and accreditation inspections.Other duties as determined by General Manager and RPC QARA management.Lead and train cross-functional teams on cGMP, aseptic techniques, and contamination control.Act as a liaison between quality, production, and regulatory teams to maintain compliance and resolve quality-related issues.Drive continuous improvement initiatives to enhance efficiency, product quality, and regulatory readinessOther duties as determined by the General Manager Qualifications and Education RequirementsBachelor’s degree in Quality Assurance, Science, Medical Sciences, Pharmacology, etc., or an equivalent combination of education and experience is requiredA minimum of 3 years in a Quality Management, Quality Assurance, or related fieldExperience in pharmacy compounding or pharma manufacturing preferredIn-depth knowledge and experience on FDA and applicable laws and regulations, as they relate to the industry, as well as of CGMP standards 21 CFR 210 and 211Strong understanding of quality management principles and proceduresProficiency in quality systems, CAPA management, and data-driven decision makingStrong verbal and written communication skills (including analysis, interpretation, and reasoning)Ability to develop and maintain collaborative relationships with peers and colleagues across the organization, as well as internal and external stakeholdersAbility to work well autonomously and within a team in a fast-paced and deadline-oriented environmentSelf-motivated with critical attention to detail, deadlines, and reportingExceptional work ethicSkillsGmp, Capa, Audit, Fda, Cgmp, Pharmaceutical, SopTop Skills DetailsGmp,Capa,Audit,FdaAdditional Skills &amp; QualificationsKnowledge, Skills &amp; AbilitiesThorough knowledge of FDA regulations, including 21 CFR Parts 210 and 211.Strong understanding of quality management systems, CAPA programs, deviation investigations, and change control processes.Experience with environmental monitoring, sterility assurance, validation, and contamination control programs.Ability to analyze data, identify trends, and make risk-based quality decisions.Excellent verbal and written communication skills.Strong organizational, problem-solving, and project management abilities.Ability to build collaborative relationships across departments and with external partners.Self-motivated with exceptional attention to detail and strong follow-through.Ability to thrive in a fast-paced, highly regulated environment.Demonstrated commitment to quality, compliance, and continuous improvement.Experience LevelIntermediate LevelJob Type &amp; LocationThis is a Permanent position based out of Hoover, AL.Pay and BenefitsThe pay range for this position is $110000.00 - $140000.00/yr.Competitive benefits offered by the companyWorkplace TypeThis is a fully onsite position in Hoover,AL.Application DeadlineThis position is anticipated to close on Aug 7, 2026.About Actalent 

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



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



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



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



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



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

Job Title: Quality SupervisorJob DescriptionWe are seeking a dynamic and proactive Quality Supervisor to manage quality control processes and oversee daily operations on the second shift. This role involves investigating root causes, problem-solving, and ensuring adherence to quality standards. You'll be a go-getter, overseeing hourly challenges.<ul><li>Act as a front-line liaison to production supervisors and staff in troubleshooting, root cause analysis, and implementing corrective actions on quality issues affecting production.</li><li>Assist in planning quality control engineering assignments and coordinate tasks for technicians, inspectors, and associate-level engineers.</li><li>Ensure quality standards are met by all outside vendors and internal departments.</li><li>Coordinate quality aspects for new product development, including on-site start-ups and tool and vendor certifications.</li><li>Design or specify inspection and testing mechanisms and equipment, and establish critical features and supporting process control information.</li><li>Develop and maintain inspection criteria for critical product features.</li><li>Analyze production limitations and standards, recommending revisions of specifications when necessary.</li><li>Assist in formulating quality control policies and procedures.</li><li>Evaluate progress and results, recommending changes in procedures or objectives as needed.</li><li>Develop and implement quality control training and mentoring for technicians.</li><li>Operate within an approved budget while maintaining a safe and healthy work environment.</li><li>Maintain a neat, clean, and orderly 5S work area.</li><li>Perform other miscellaneous duties as assigned.</li></ul>Essential Skills<ul><li>Quality assurance</li><li>Root cause analysis</li><li>People focus</li><li>Quality engineering</li><li>Quality control</li><li>Quality management</li></ul>Additional Skills &amp; Qualifications<ul><li>Three or more years of experience in quality, process engineering, or an equivalent field, preferably in the automotive or similar assembly industry.</li><li>Strong process improvement experience, including PFMEA, control plans, RCCA (8D), CAR/CAPA, DOE, gage R&amp;R, PPAP, engineering drawing, GD&amp;T, product failure analysis, and Quality Management Systems (QMS).</li><li>Strong problem-solving and communication skills.</li><li>Ability to work in a fast-paced manufacturing environment, being a self-starter capable of independent work.</li><li>Demonstrated Black Belt knowledge; experience with Six Sigma methods/tools and Lean Manufacturing is preferred.</li><li>Bachelor's degree in Engineering or a related technical field is required.</li></ul>Work EnvironmentThe role involves supervising a team of 10-15 people on the second shift, focusing on final assembly and production. The position requires quick problem-solving skills with a focus on torque failures and paint issues. The work environment is fast-paced, requiring effective communication and collaboration with on-call team members. The dress code is casual, and the facility promotes a clean and orderly 5S workspace.Job Type &amp; LocationThis is a Permanent position based out of Madison, AL.Pay and BenefitsThe pay range for this position is $80000.00 - $90000.00/yr.401, dental, medical, profit sharing,Workplace TypeThis is a fully onsite position in Madison,AL.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 Supervisor

Job Title: Quality Supervisor and Quality Engineer(US Citizen/Permanent Resident Due To ITAR)Job DescriptionThe Quality Manager is responsible for leading the Quality Engineering team, ensuring the integration of quality standards across all value streams. This role emphasizes consistent workmanship through training, feedback, and accountability while monitoring key metrics such as scrap, MRB, non-conformance, and in-process corrections.Responsibilities<ul><li>Lead, develop, and train a high-performing Quality Team with regular feedback and coaching.</li><li>Monitor and report on scrap, MRB, non-conformance, and in-process correction by value stream.</li><li>Conduct departmental reporting and lead tier 1 &amp; 2, while supporting tier 3.</li><li>Deliver targeted improvements towards scrap, MRB, non-conformance, and in-process correction by value stream.</li><li>Standardize quality standards and processes.</li><li>Lead customer complaints, corrective &amp; preventative actions, and root cause analysis for sustainable quality improvements.</li><li>Identify opportunities for continuous improvement.</li><li>Support and/or lead quality Kaizen.</li><li>Support new product introduction.</li><li>Analyze trends, address production issues, and escalate risks impacting customers, products, schedules, or the supply chain.</li><li>Oversee customer complaints, lead corrective actions, and drive problem-solving initiatives while standardizing quality processes.</li></ul>Essential Skills<ul><li>3+ years of experience as a Quality Engineer.</li><li>Bachelor's degree in Engineering.</li><li>Strong understanding of quality systems.</li><li>Experience with statistical process control and trend analysis.</li><li>Lean Manufacturing expertise.</li><li>Experience with root cause analysis and corrective action processes (e.g., 8D, Fishbone, 5-Why).</li><li>Proficiency in statistical software such as SQC Pack or Minitab®.</li><li>Understanding of control plans.</li><li>Exposure to continuous improvement.</li><li>Familiarity with new product introduction.</li><li>Previous leadership experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>ASQ CQE certification or equivalent experience is preferred.</li><li>Proficient in measurement, inspection, and testing methods, calibration.</li><li>Familiarity with government contracts (DOD).</li><li>Familiarity with regulatory compliance in relevant industries (e.g., FDA, AS9100, IATF).</li></ul>Work EnvironmentThe work environment offers a recently remodeled facility with a game room area and an extremely clean manufacturing environment. The role involves 50% on-floor time and managing five direct reports. The company is passionate about its mission and its products, which directly impact lives. There is a focus on implementing more automation in the facility, and the team is excited about new projects, including new foam formulations, chin straps, helmets, and shelJob Type &amp; LocationThis is a Contract to Hire position based out of Cleveland, OH.Pay and BenefitsThe pay range for this position is $43.00 - $58.00/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 Cleveland,OH.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 Supervisor And Quality Engineer (2 Positions) (US Citizen/Permanent Resident -ITAR)

Job Title: Quality Systems / Document Control Contractor Job DescriptionThis role supports Quality Systems and Compliance by managing electronic and paper-based documentation within a regulated biotechnology manufacturing environment. The contractor maintains controlled documents, batch records, and training assignments using validated electronic document management systems, while ensuring adherence to GMP, GDP, and data integrity requirements. The position offers broad exposure to Quality Systems beyond document control, cross-functional collaboration, and the opportunity to contribute to a lean, high-impact Quality organization.Responsibilities<ul><li>Support Quality Systems and Compliance through electronic document management, document control, batch record issuance, training administration, and physical record reconciliation.</li><li>Process controlled documents within validated electronic document management systems such as Compliance Plus or comparable platforms, ensuring accuracy and compliance.</li><li>Manage the routing, review, approval, issuance, and revision control of documents, maintaining complete traceability throughout the document lifecycle.</li><li>Support the creation, processing, and maintenance of SOPs, controlled forms, policies, procedures, logbooks, batch records, CAPA-related documents, deviations, and change controls.</li><li>Maintain and organize paper-based quality records, including archival activities, to ensure records are complete, retrievable, and audit-ready.</li><li>Issue identifiers for controlled documents, batch records, and other quality records, ensuring proper numbering control and version management.</li><li>Oversee batch record issuance and numbering control to support manufacturing and lot traceability requirements.</li><li>Ensure compliance with GMP documentation requirements, including version control, controlled-copy management, and adherence to data integrity principles.</li><li>Verify lot numbers and maintain traceability to support quality investigations, batch disposition, and regulatory expectations.</li><li>Perform quality record reconciliation to confirm that documentation is complete, accurate, and aligned with manufacturing and quality activities.</li><li>Administer training assignments within the training management system, ensuring that personnel receive and complete required training on time.</li><li>Provide cross-functional document control and quality systems support to Quality, Manufacturing, Regulatory, Clinical, Facilities, and Quality Control teams.</li><li>Adapt to fast-changing priorities while maintaining high accuracy and attention to detail in all documentation activities.</li><li>Participate in potential future eQMS implementation activities, contributing to system setup, document migration, and process improvements.</li><li>Demonstrate a team-first mentality by collaborating closely with a lean Quality team and providing customer-service-oriented support to internal stakeholders.</li></ul>Essential Skills<ul><li>Experience with electronic document management systems (EDMS) and quality management systems (QMS) in a regulated environment.</li><li>Hands-on experience with validated document management systems such as Veeva, TrackWise, MasterControl, Compliance Plus, or comparable platforms.</li><li>Strong understanding of GMP (Good Manufacturing Practice) and GDP (Good Documentation Practice) requirements.</li><li>Knowledge of data integrity principles and their application to quality records and documentation.</li><li>Experience with document routing, review, approval, issuance, revision control, archival, and traceability.</li><li>Proficiency in SOP processing and management of controlled forms, policies, procedures, and logbooks.</li><li>Experience with batch record issuance, numbering control, and GMP documentation requirements.</li><li>Ability to manage version control and controlled-copy distribution for quality documents.</li><li>Familiarity with lot number verification and traceability processes within a manufacturing environment.</li><li>Experience in quality record reconciliation and training assignment administration.</li><li>Strong GMP mindset with excellent attention to detail and accuracy.</li><li>Coachable, eager to learn, and able to support repetitive and manual record-management activities.</li><li>Ability to work effectively in a lean biotechnology environment with high manufacturing activity.</li><li>Team-first mentality, reliability, and strong motivation to contribute to long-term organizational success.</li><li>Comfortable working onsite five days per week during standard business hours.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in biotechnology or pharmaceutical manufacturing environments.</li><li>Familiarity with training management systems and eQMS platforms.</li><li>Exposure to CAPA, change control, deviations, and other quality systems processes.</li><li>Interest in participating in future eQMS implementation projects and continuous improvement initiatives.</li><li>Strong organizational and time-management skills to handle fast-changing priorities.</li><li>Customer-service-oriented approach when supporting cross-functional teams in Quality, Manufacturing, QC, Clinical, Regulatory, and Facilities.</li><li>Desire for significant development opportunities in Quality Systems and potential conversion to a longer-term role.</li></ul>Work EnvironmentThe role is based in an early-stage biotechnology company located in Redwood City, CA, within a lean Quality organization of approximately four team members. The position is full-time and onsite five days per week, with preferred onsite availability from around 9:00 a.m. to 4:00 p.m. The environment involves high manufacturing activity and fast-changing priorities, requiring a high level of accountability for accuracy and compliance. The culture is collaborative and customer-service-oriented, with close cross-functional interaction across Quality, Manufacturing, QC, Clinical, Regulatory, and Facilities. The setting emphasizes hands-on work, direct mentorship, and broad exposure to Quality Systems and biotechnology manufacturing.Job Type &amp; LocationThis is a Contract to Hire position based out of Redwood City, CA.Pay and BenefitsThe pay range for this position is $51.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Systems / Document Control Contractor

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