QA Analyst
Not Disclosed•ContractorOn-site
location_on22157, Newkirk Avenue, Keystone, Carson, Los Angeles County, California, 90745, United States
About the Team
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.
About the Role
The Quality Analyst serves as a critical partner to production, procurement, and safety teams within a laboratory-based environment. This role exists to ensure consistent product quality by conducting analytical testing, documenting results, and recommending corrective actions. You will be the guardian of compliance, ensuring that all site activities adhere to strict standards and procedures.
In this position, you will operate primarily in a laboratory setting within a production facility, supporting manufacturing and packaging operations with timely testing and results. Your day involves performing benchtop analyses and utilizing advanced instruments to test raw materials and finished products. You will collaborate closely with cross-functional teams to implement plans that improve the quality of materials and drive continuous improvement through loss analysis. The role requires a methodical approach to data, ensuring that all logs, worksheets, and records are accurate to support traceability and analysis.
Hiring Process
This is a contract position based out of Long Beach, CA. The application deadline for this opportunity is anticipated to be June 12, 2026. Please note that no immigration sponsorship is available for this role.
Equal Opportunity & Culture
Actalent 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 other characteristic protected by law. We promote a collaborative atmosphere focused on quality, continuous improvement, and professional development, with a strong emphasis on safety culture.
If you would like to request a reasonable accommodation due to a disability, please email actalentaccommodation@actalentservices.com.
Note: 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.
Work location
Work model: On-site
22157, Newkirk Avenue, Keystone, Carson, Los Angeles County, California, 90745, United States
Carson, California
Key Responsibilities
- check_circleDocument and trend analytical results in compliance with quality and regulatory standards
- check_circleConduct investigations for test deviations and implement corrective actions
- check_circleMaintain laboratory equipment and perform preventive maintenance procedures
- check_circleCollaborate with procurement to ensure quality of raw and packaging materials
- check_circleEnsure compliance with safety, GMP, and GLP standards in laboratory operations
- check_circleManage quality data and documentation using SAP and Microsoft Office systems
- check_circlePerform analytical testing using HPLC, gas chromatography, and titration methods
- check_circleTest raw materials and finished products to support manufacturing timelines
Requirements
- verifiedBachelor's degree in life sciences, chemistry, or another relevant science discipline
- verified3+ years of production experience in a food, chemical, beverage, or related batch manufacturing environment
- verifiedExperience with analytical techniques including titration, conductivity, specific gravity, pH, FTIR, spectrophotometry, fluorescence, atomic absorption (AA), HPLC, and gas chromatography
- verifiedProficiency with Microsoft Office applications (PowerPoint, Excel, Word)
- verifiedSAP experience in a production or quality environment
- verifiedNo immigration sponsorship is available
Nice to Have
Experience working in a laboratory environment within a manufacturing or production facility. Familiarity with quality control, quality assurance, and good manufacturing practice (GMP) principles. Understanding of good laboratory practice (GLP) and safe working practices in a lab setting. Experience with loss analysis and continuous improvement methods to identify savings and efficiency opportunities. Comfort with data entry and electronic documentation in quality systems. Ability to collaborate effectively with cross-functional teams such as production, procurement, and safety. Strong attention to detail and a methodical approach to testing and documentation. Capability to role model positive behaviors and support a culture of safety, quality, and accountability.
Benefits & Perks
check_circleMedical, dental, and vision insurancecheck_circleCritical Illness, Accident, and Hospital insurancecheck_circle401(k) Retirement Plan with pre-tax and Roth post-tax contributionscheck_circleVoluntary Life and AD&D insurance for employee and dependentsShort and long-term disability insurance
Similar Job Opportunities
Skills, education and keywords
Skills: Analytical Chemistry, Titration, Conductivity, Specific Gravity, PH, Ftir, Spectrophotometry, Fluorescence, Atomic Absorption, HPLC.
Education: Bachelor's degree in life sciences, chemistry, or another relevant science discipline required.
Frequently asked questions about QA Analyst at Actalent
What does a QA Analyst at Actalent do?expand_more
Day-to-day, the QA Analyst at Actalent will document and trend analytical results in compliance with quality and regulatory standards; conduct investigations for test deviations and implement corrective actions; maintain laboratory equipment and perform preventive maintenance procedures; and collaborate with procurement to ensure quality of raw and packaging materials.
What are the requirements for this QA Analyst role?expand_more
To qualify for the QA Analyst at Actalent position, applicants should have: Bachelor's degree in life sciences, chemistry, or another relevant science discipline; 3+ years of production experience in a food, chemical, beverage, or related batch manufacturing environment; Experience with analytical techniques including titration, conductivity, specific gravity, pH, FTIR, spectrophotometry, fluorescence, atomic absorption (AA), HPLC, and gas chromatography; Proficiency with Microsoft Office applications (PowerPoint, Excel, Word); SAP experience in a production or quality environment; and No immigration sponsorship is available.
Where is the QA Analyst role at Actalent located?expand_more
QA Analyst at Actalent is based in 22157, Newkirk Avenue, Keystone, Carson, Los Angeles County, California, 90745, United States. This is a on-site role.
Is this QA Analyst job remote, hybrid, or on-site?expand_more
Actalent has listed this QA Analyst role as on-site.
How much experience is required for this QA Analyst role?expand_more
QA Analyst at Actalent typically requires 3+ years of relevant experience at the mid level level.
What skills do you need for the QA Analyst role at Actalent?expand_more
Key skills for QA Analyst at Actalent include Analytical Chemistry; Titration; Conductivity; Specific Gravity; PH; Ftir; Spectrophotometry; and Fluorescence.
What education is required for QA Analyst at Actalent?expand_more
Educational requirements for this role: Bachelor's degree in life sciences, chemistry, or another relevant science discipline required.
What category does the QA Analyst role belong to?expand_more
QA Analyst at Actalent is part of the scientific & qa job category on Recrutus.