Quality Assurance Jobs at Eurofins, USA
Eurofins is hiring a Pharmaceutical Manufacturing QA Associate to support GMP-compliant manufacturing operations at its Sanford, North Carolina, facility. This is a full-time, on-site role. The Quality Assurance Jobs at Eurofins are ideal for professionals with experience in Quality Assurance within pharmaceutical or biopharmaceutical environments. The position focuses on real-time batch record review, deviation management, GMP walkthroughs, and shop-floor quality decision-making to ensure regulatory compliance and product integrity.
Job Details:
- Job Title: Pharmaceutical Manufacturing QA Associate
- Location: Sanford, North Carolina, USA
- Employment Type: Full-time
- Work Schedule: Monday – Friday | 8:00 AM – 5:00 PM
- Industry: Pharmaceutical Manufacturing / Quality Assurance
- Work Mode: On-site
About the Company:
Eurofins Scientific is a global leader in life sciences, providing analytical testing services across pharmaceuticals, food, environment, cosmetics, and clinical diagnostics. Founded in France, Eurofins has grown into a worldwide network of 900+ laboratories across 54 countries, employing more than 58,000 professionals. The company supports pharmaceutical development, manufacturing, and regulatory compliance through scientific excellence, innovation, and data integrity.
Educational Requirements for the QA Associate Role:
- Bachelor’s or Master’s degree in Microbiology, Biological Sciences, Bioengineering, or a related discipline
- Bachelor’s degree + 2–4 years of relevant experience
- Master’s degree + up to 2 years of relevant experience
Relevant experience includes:
- Quality Assurance in GMP-regulated pharmaceutical manufacturing
- Batch record review and GMP documentation
- Deviation, change control, CAPA, and analytical data review
Key Responsibilities of the QA Associate:
- Perform real-time batch record and manufacturing documentation review
- Initiate and support deviations and investigations on the shop floor
- Conduct GMP walkthroughs and housekeeping inspections
- Support the transfer of Master Cell Banks to manufacturing
- Execute or review room and line clearances
- Make real-time quality decisions per ICH Q7 and 21 CFR Part 211
- Participate in cross-functional teams to meet project timelines
- Draft, review, and update Standard Operating Procedures (SOPs)
- Support facility start-up, continuous operations, and compliance activities
Skills Required for the QA Associate Role:
- Strong understanding of GMP regulations and pharmaceutical QA processes
- Experience with batch record review and documentation compliance
- Knowledge of data integrity principles
- Ability to review and investigate deviations, CAPAs, and change controls
- Analytical thinking and attention to detail
- Strong communication and teamwork skills
- Ability to make independent quality decisions in real time
Benefits of the Quality Assurance Jobs at Eurofins:
- Comprehensive Medical, Dental, and Vision Insurance
- Life and Disability Insurance
- 401(k) Retirement Plan with Company Match
- Paid Vacation and Holidays
- Stable Monday–Friday work schedule
- Opportunity to work with a global life sciences leader
- Inclusive workplace supporting Veteran and Disabled Equal Employment Opportunities
