24 General Motors jobs in St. Charles

Job Title: Quality Control Technician
Job Description
As a Quality Control Technician, you will perform essential testing within a production lab, focusing on wet chemistry testing, gas chromatography (GC) testing, viscosity, and color testing. Your work will primarily involve final product testing release, and you will have the opportunity to cross-train across different product lines and labs to support diverse company needs.
Responsibilities
+ Conduct wet chemistry testing, titration, and GC testing to ensure quality control.
+ Perform specific tests such as viscosity, loss on heating (LOH), specific gravity, and melting point.
+ Handle testing of a variety of products, including rubber tire additives, oil additives, and chlorine-based products.
+ Operate auto titrators and perform visual color testing.
+ Input samples and test results into Sample Manager and ensure final results are recorded in SAP.
+ Train on and execute highly specific tests, ensuring accuracy in all processes.
Essential Skills
+ Experience in a lab environment with a focus on analytical chemistry.
+ Proficiency in gas chromatography and basic wet chemistry procedures.
+ Ability to perform titrations and manage quality control processes.
+ Experience in troubleshooting within a laboratory setting.
Additional Skills & Qualifications
+ Bachelor's Degree or equivalent experience; at least 1-3 years of lab experience is preferred.
+ Experience in any industry related to pharma or chemical sectors is advantageous.
+ Experience in chemical industry wet chemistry testing is beneficial.
+ Willingness to learn and adapt to new standards and procedures.
Work Environment
The work environment is a production lab setting with a variety of substances, including oily materials. The lab is divided into different sections, offering a dynamic atmosphere for learning and skill growth. While the facility is well-maintained, it is not a pharmaceutical-grade cleanroom. Strong smells are present, and uniforms are provided. The lab is equipped with both new and older technology, offering a broad scope of experience.
Job Type & Location
This is a Contract to Hire position based out of Sauget, Illinois.
Pay and Benefits
The pay range for this position is $27.00 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Sauget,IL.
Application Deadline
This position is anticipated to close on Oct 20, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.

Quality Control Technician
Job Description
As a Quality Control Technician, you will perform essential testing within a production lab, focusing on wet chemistry testing, gas chromatography (GC) testing, viscosity, and color testing. Your work will primarily involve final product testing release, and you will have the opportunity to cross-train across different product lines and labs to support diverse company needs.
Responsibilities
+ Conduct wet chemistry testing, titration, and GC testing to ensure quality control.
+ Perform specific tests such as viscosity, loss on heating (LOH), specific gravity, and melting point.
+ Handle testing of a variety of products, including rubber tire additives, oil additives, and chlorine-based products.
+ Operate auto titrators and perform visual color testing.
+ Input samples and test results into Sample Manager and ensure final results are recorded in SAP.
+ Train on and execute highly specific tests, ensuring accuracy in all processes.
Essential Skills
+ Experience in a lab environment with a focus on analytical chemistry.
+ Proficiency in gas chromatography and basic wet chemistry procedures.
+ Ability to perform titrations and manage quality control processes.
+ Experience in troubleshooting within a laboratory setting.
Additional Skills & Qualifications
+ Bachelor's Degree or equivalent experience; at least 1-3 years of lab experience is preferred.
+ Experience in any industry related to pharma or chemical sectors is advantageous.
+ Experience in chemical industry wet chemistry testing is beneficial.
+ Willingness to learn and adapt to new standards and procedures.
Work Environment
The work environment is a production lab setting with a variety of substances, including oily materials. The lab is divided into different sections, offering a dynamic atmosphere for learning and skill growth. While the facility is well-maintained, it is not a pharmaceutical-grade cleanroom. Strong smells are present, and uniforms are provided. The lab is equipped with both new and older technology, offering a broad scope of experience.
Job Type & Location
This is a Contract to Hire position based out of Sauget, Illinois.
Pay and Benefits
The pay range for this position is $27.00 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Sauget,IL.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.

**Job Title:** Quality Control Inspector
**Location:** Saint Louis, MO
**Pay Rate:** 26/hour
**Schedule:** 1st shift
**Position Summary**
We are seeking a detail-oriented Quality Control Inspector to join our aerospace manufacturing team. The ideal candidate will possess a strong understanding of AS9100 standards, demonstrate technical proficiency in inspection processes, and maintain a commitment to accuracy and compliance. The Quality Inspector is integral to ensuring our products meet stringent customer and industry requirements.
**Key Responsibilities**
+ Perform layout inspections using surface plates, blocks, parallels, clamps, and precision instruments (micrometers, calipers, height gauges)
+ Conduct first article inspections (FAI), in-process checks, receiving inspections, and final part inspections in accordance with engineering drawings and technical specifications
+ Interpret complex blueprints, specifications, and Geometric Dimensioning and Tolerancing (GD&T) requirements
+ Identify, segregate, and document nonconforming materials; initiate nonconformance reports (NCRs)
+ Support root cause analysis and implementation of corrective and preventive actions (CAPA) in response to quality issues
+ Apply acceptance stamps to conforming products and ensure traceability
+ Perform in-process audits to verify compliance with AS9100 standards and internal procedures
+ Calibrate, verify, and maintain inspection and measuring equipment
+ Accurately complete and maintain inspection records and reports, both digital and paper
+ Verify measurement data recorded on Statistical Process Control (SPC) sheets
+ Collaborate with customer source inspectors during source inspection activities
**Qualifications**
+ High school diploma or equivalent required
+ Completion of technical/trade school or relevant vocational training preferred
+ Minimum two years of experience in aerospace manufacturing inspection or related quality control role
+ Proficient in reading engineering drawings and using inspection tools and equipment
+ Familiarity with AS9100 Quality Management System requirements
+ Working knowledge of GD&T (Geometric Dimensioning and Tolerancing)
+ Detail-oriented with strong organizational and documentation skills
+ Effective communicator with ability to work independently and in cross-functional teams
+ Must be a U.S. Person in accordance with ITAR/EAR regulations (U.S. Citizen or U.S. Permanent Resident)
**Bonus Qualifications:**
+ Experience using FaroArm to perform 3D inspection and measurement of parts and assemblies
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
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Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

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Quality Control Technician - Food Manufacturing
Chesterfield, Missouri | Contract-to-Hire | Full-Time
Play a Key Role in Ensuring Food Safety & Quality Excellence
We're seeking a detail-driven Quality Control Technician to join our team and help uphold the highest standards in food safety, regulatory compliance, and product quality. If you're passionate about precision, thrive in fast-paced environments, and want to make a real impact in the food industry-this is the role for you!
What You'll Do
+ Conduct pre-operational inspections and environmental swabbing (air, water, equipment surfaces) to ensure sanitary conditions.
+ Perform routine line checks for packaging, labeling, coding, sealing, and metal detection/X-ray systems.
+ Collect and test samples for microbial and chemical analysis to verify product safety and consistency.
+ Calibrate and maintain lab equipment including thermometers and moisture analyzers.
+ Review production data and operator check sheets for accuracy and compliance.
+ Monitor GMP compliance on the production floor and assist with staff training initiatives.
+ Investigate and document non-conformances, customer complaints, and CAPAs (Corrective and Preventive Actions).
+ Maintain detailed QA records and support internal/external audits.
+ Assist in shelf-life studies, product bake-offs, and texture analysis.
+ Contribute to continuous improvement and SOP development.
What You Bring
+ High School Diploma or equivalent (Associate's or Bachelor's in a science field is a plus).
+ Minimum 1 year of experience in food manufacturing or QA/QC.
+ Familiarity with HACCP, GMP, GFSI, and food safety regulations.
+ Proficiency in Microsoft Office (Excel, Word, Outlook).
+ Certifications such as HACCP, SQF, or PCQI are a strong advantage.
+ Chemistry or GMP preferred.
Work Environment
+ Exposure to typical food production conditions: cold, wet, noisy, and allergen-rich environments.
+ Physical activity required: standing, walking, lifting (up to 50 lbs), bending, climbing, and more.
+ Flexible schedule including nights, weekends, holidays, and overtime as needed.
+ Standard hours: Monday-Friday, 6 AM to 2:30 PM in lab, manufacturing, and office settings.
Why Join Us?
+ Be part of a team that values quality, safety, and innovation.
+ Gain hands-on experience in a regulated, fast-paced industry.
+ Opportunity to grow into a permanent role with long-term career potential.
Pay and Benefits
The pay range for this position is $19.00 - $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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Chesterfield,MO.
Application Deadline
This position is anticipated to close on Oct 20, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.

Quality Control Lab Technician
Job Description
As a Quality Control Technician, you will perform laboratory testing and related quality control activities using various instruments such as Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, HPLC, GC, IC, ICP, Flame AA, TOC, and Conductivity meter. Your role will ensure compliance with applicable SOPs and cGMPs. You will provide timely testing and notify management of any aberrant occurrences that may impact manufactured or marketed products.
Responsibilities
+ Ensure a safe and quality working environment through training, awareness, and compliance with Safety/Quality guidelines and SOPs.
+ Maintain the department, premises, and equipment.
+ Complete all necessary training to perform assigned tasks confidently and consistently.
+ Perform all work in compliance with site safety and radiation protection guidelines.
+ Collaborate with team members to ensure timely completion of quality tasks.
+ Attend mandatory trainings as required by site regulatory requirements and management.
+ Assist with investigations by providing testing results and communication of practices.
+ Aid in the training and development of employees.
Essential Skills
+ Proficiency in chemistry, laboratory techniques, biology, and biochemistry.
+ Ability to work independently and collaboratively to achieve goals and priorities.
+ Flexibility and strong teamwork skills.
+ Capability to adjust to changing priorities and schedules.
+ High level of energy and regular, consistent attendance.
Additional Skills & Qualifications
+ Ability to lift 70 pounds, walk, bend, stoop, push, pull, reach, and climb stairs with or without accommodation.
+ Knowledge of wet chemistry and analytical techniques.
+ 2 years of college-level science or an AS Degree in Science is required. A BS Degree in Science is preferred.
+ Experience with various laboratory instruments such as Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, HPLC, GC, IC, ICP, Flame AA, TOC, and Conductivity meter.
Work Environment
The shift for this position is Saturday to Tuesday, 7:00 PM to 5:30 AM. You will work in a plant that produces radioactive materials, requiring participation in safety programs designed to minimize exposure levels. Responsibilities include the ability to lift 70 pounds and perform physical tasks such as walking, bending, stooping, pushing, pulling, reaching, and climbing stairs with or without accommodation. You must be willing to wear a variety of personal protective equipment. The job offers a shift differential upon conversion, which can be up to $3,000 in annual compensation, and includes holiday pay. The schedule is 4 days of 10-hour shifts, offering a longer break during the week. This role provides the opportunity to learn various standard instrumentation or methods in a pharma QC Lab, including unique instrumentation specific to working with radioactive materials.
Job Type & Location
This is a Contract to Hire position based out of Maryland Heights, Missouri.
Pay and Benefits
The pay range for this position is $2.00 - 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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Maryland Heights,MO.
Application Deadline
This position is anticipated to close on Oct 20, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.

x
Quality Control Technician - Food Manufacturing
Chesterfield, Missouri | Contract-to-Hire | Full-Time
Play a Key Role in Ensuring Food Safety & Quality Excellence
We're seeking a detail-driven Quality Control Technician to join our team and help uphold the highest standards in food safety, regulatory compliance, and product quality. If you're passionate about precision, thrive in fast-paced environments, and want to make a real impact in the food industry-this is the role for you!
What You'll Do
+ Conduct pre-operational inspections and environmental swabbing (air, water, equipment surfaces) to ensure sanitary conditions.
+ Perform routine line checks for packaging, labeling, coding, sealing, and metal detection/X-ray systems.
+ Collect and test samples for microbial and chemical analysis to verify product safety and consistency.
+ Calibrate and maintain lab equipment including thermometers and moisture analyzers.
+ Review production data and operator check sheets for accuracy and compliance.
+ Monitor GMP compliance on the production floor and assist with staff training initiatives.
+ Investigate and document non-conformances, customer complaints, and CAPAs (Corrective and Preventive Actions).
+ Maintain detailed QA records and support internal/external audits.
+ Assist in shelf-life studies, product bake-offs, and texture analysis.
+ Contribute to continuous improvement and SOP development.
What You Bring
+ High School Diploma or equivalent (Associate's or Bachelor's in a science field is a plus).
+ Minimum 1 year of experience in food manufacturing or QA/QC.
+ Familiarity with HACCP, GMP, GFSI, and food safety regulations.
+ Proficiency in Microsoft Office (Excel, Word, Outlook).
+ Certifications such as HACCP, SQF, or PCQI are a strong advantage.
+ Chemistry or GMP preferred.
Work Environment
+ Exposure to typical food production conditions: cold, wet, noisy, and allergen-rich environments.
+ Physical activity required: standing, walking, lifting (up to 50 lbs), bending, climbing, and more.
+ Flexible schedule including nights, weekends, holidays, and overtime as needed.
+ Standard hours: Monday-Friday, 6 AM to 2:30 PM in lab, manufacturing, and office settings.
Why Join Us?
+ Be part of a team that values quality, safety, and innovation.
+ Gain hands-on experience in a regulated, fast-paced industry.
+ Opportunity to grow into a permanent role with long-term career potential.
Pay and Benefits
The pay range for this position is $19.00 - $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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Chesterfield,MO.
Application Deadline
This position is anticipated to close on Oct 18, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.

Quality Control Technician - Food Manufacturing
Chesterfield, Missouri | Contract-to-Hire | Full-Time
Play a Key Role in Ensuring Food Safety & Quality Excellence
We're seeking a detail-driven Quality Control Technician to join our team and help uphold the highest standards in food safety, regulatory compliance, and product quality. If you're passionate about precision, thrive in fast-paced environments, and want to make a real impact in the food industry-this is the role for you!
What You'll Do
+ Conduct pre-operational inspections and environmental swabbing (air, water, equipment surfaces) to ensure sanitary conditions.
+ Perform routine line checks for packaging, labeling, coding, sealing, and metal detection/X-ray systems.
+ Collect and test samples for microbial and chemical analysis to verify product safety and consistency.
+ Calibrate and maintain lab equipment including thermometers and moisture analyzers.
+ Review production data and operator check sheets for accuracy and compliance.
+ Monitor GMP compliance on the production floor and assist with staff training initiatives.
+ Investigate and document non-conformances, customer complaints, and CAPAs (Corrective and Preventive Actions).
+ Maintain detailed QA records and support internal/external audits.
+ Assist in shelf-life studies, product bake-offs, and texture analysis.
+ Contribute to continuous improvement and SOP development.
What You Bring
+ High School Diploma or equivalent (Associate's or Bachelor's in a science field is a plus).
+ Minimum 1 year of experience in food manufacturing or QA/QC.
+ Familiarity with HACCP, GMP, GFSI, and food safety regulations.
+ Proficiency in Microsoft Office (Excel, Word, Outlook).
+ Certifications such as HACCP, SQF, or PCQI are a strong advantage.
+ Background in Chemistry or GMP preferred.
Work Environment
+ Exposure to typical food production conditions: cold, wet, noisy, and allergen-rich environments.
+ Physical activity required: standing, walking, lifting (up to 50 lbs), bending, climbing, and more.
+ Flexible schedule including nights, weekends, holidays, and overtime as needed.
+ Standard hours: Monday-Friday, 6 AM to 2:30 PM in lab, manufacturing, and office settings.
Why Join Us?
+ Be part of a team that values quality, safety, and innovation.
+ Gain hands-on experience in a regulated, fast-paced industry.
+ Opportunity to grow into a permanent role with long-term career potential.
Pay and Benefits
The pay range for this position is $19.00 - $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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Chesterfield,MO.
Application Deadline
This position is anticipated to close on Oct 17, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.

Quality Control Lab Technician
Job Description
As a Quality Control Technician, you will perform laboratory testing and related quality control activities using various instruments such as Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, HPLC, GC, IC, ICP, Flame AA, TOC, and Conductivity meter. Your role will ensure compliance with applicable SOPs and cGMPs. You will provide timely testing and notify management of any aberrant occurrences that may impact manufactured or marketed products.
Responsibilities
+ Ensure a safe and quality working environment through training, awareness, and compliance with Safety/Quality guidelines and SOPs.
+ Maintain the department, premises, and equipment.
+ Complete all necessary training to perform assigned tasks confidently and consistently.
+ Perform all work in compliance with site safety and radiation protection guidelines.
+ Collaborate with team members to ensure timely completion of quality tasks.
+ Attend mandatory trainings as required by site regulatory requirements and management.
+ Assist with investigations by providing testing results and communication of practices.
+ Aid in the training and development of employees.
Essential Skills
+ Proficiency in chemistry, laboratory techniques, biology, and biochemistry.
+ Ability to work independently and collaboratively to achieve goals and priorities.
+ Flexibility and strong teamwork skills.
+ Capability to adjust to changing priorities and schedules.
+ High level of energy and regular, consistent attendance.
Additional Skills & Qualifications
+ Ability to lift 70 pounds, walk, bend, stoop, push, pull, reach, and climb stairs with or without accommodation.
+ Knowledge of wet chemistry and analytical techniques.
+ 2 years of college-level science or an AS Degree in Science is required. A BS Degree in Science is preferred.
+ Experience with various laboratory instruments such as Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, HPLC, GC, IC, ICP, Flame AA, TOC, and Conductivity meter.
Work Environment
The shift for this position is Saturday to Tuesday, 7:00 PM to 5:30 AM. You will work in a plant that produces radioactive materials, requiring participation in safety programs designed to minimize exposure levels. Responsibilities include the ability to lift 70 pounds and perform physical tasks such as walking, bending, stooping, pushing, pulling, reaching, and climbing stairs with or without accommodation. You must be willing to wear a variety of personal protective equipment. The job offers a shift differential upon conversion, which can be up to $3,000 in annual compensation, and includes holiday pay. The schedule is 4 days of 10-hour shifts, offering a longer break during the week. This role provides the opportunity to learn various standard instrumentation or methods in a pharma QC Lab, including unique instrumentation specific to working with radioactive materials.
Job Type & Location
This is a Contract to Hire position based out of Maryland Heights, Missouri.
Pay and Benefits
The pay range for this position is $2.00 - 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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Maryland Heights,MO.
Application Deadline
This position is anticipated to close on Oct 14, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.

Quality Control Technician
Job Description
As a Quality Control Technician, you will perform laboratory testing and related quality control activities using various instruments such as Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, HPLC, GC, IC, ICP, Flame AA, TOC, and Conductivity meter. Your role will ensure compliance with applicable SOPs and cGMPs. You will provide timely testing and notify management of any aberrant occurrences that may impact manufactured or marketed products.
Responsibilities
+ Ensure a safe and quality working environment through training, awareness, and compliance with Safety/Quality guidelines and SOPs.
+ Maintain the department, premises, and equipment.
+ Complete all necessary training to perform assigned tasks confidently and consistently.
+ Perform all work in compliance with site safety and radiation protection guidelines.
+ Collaborate with team members to ensure timely completion of quality tasks.
+ Attend mandatory trainings as required by site regulatory requirements and management.
+ Assist with investigations by providing testing results and communication of practices.
+ Aid in the training and development of employees.
Essential Skills
+ Proficiency in chemistry, laboratory techniques, biology, and biochemistry.
+ Ability to work independently and collaboratively to achieve goals and priorities.
+ Flexibility and strong teamwork skills.
+ Capability to adjust to changing priorities and schedules.
+ High level of energy and regular, consistent attendance.
Additional Skills & Qualifications
+ Ability to lift 70 pounds, walk, bend, stoop, push, pull, reach, and climb stairs with or without accommodation.
+ Knowledge of wet chemistry and analytical techniques.
+ 2 years of college-level science or an AS Degree in Science is required. A BS Degree in Science is preferred.
+ Experience with various laboratory instruments such as Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, HPLC, GC, IC, ICP, Flame AA, TOC, and Conductivity meter.
Work Environment
The shift for this position is Saturday to Tuesday, 7:00 PM to 5:30 AM. You will work in a plant that produces radioactive materials, requiring participation in safety programs designed to minimize exposure levels. Responsibilities include the ability to lift 70 pounds and perform physical tasks such as walking, bending, stooping, pushing, pulling, reaching, and climbing stairs with or without accommodation. You must be willing to wear a variety of personal protective equipment. The job offers a shift differential upon conversion, which can be up to $3,000 in annual compensation, and includes holiday pay. The schedule is 4 days of 10-hour shifts, offering a longer break during the week. This role provides the opportunity to learn various standard instrumentation or methods in a pharma QC Lab, including unique instrumentation specific to working with radioactive materials.
Job Type & Location
This is a Contract to Hire position based out of Maryland Heights, Missouri.
Pay and Benefits
The pay range for this position is $2.00 - 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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Maryland Heights,MO.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.