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Pharmaceutical Manufacturing QA Associate
Job in
Sanford, Lee County, North Carolina, 27330, USA
Listed on 2026-01-04
Listing for:
Eurofins PSS Insourcing Solutions
Full Time
position Listed on 2026-01-04
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst
Job Description & How to Apply Below
Pharmaceutical Manufacturing QA Associate
Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services across multiple industries to make life and our environment safer, healthier and more sustainable.
Job Description CORE JOB DUTIES- Performs duties with the guidance of Sr. Associates
- Execute real time review of batch documentation and other manufacturing documentation analyzing for errors, corrections, and compliance
- Support Transfer Master Cell Banks to Manufacturing
- Perform housekeeping and GMP walkthroughs of facility
- Initiate deviations in real time and assists in investigations
- Work in cross functional teams to meet and exceed timelines
- Execute or review room and line clearances
- Makes quality decision in real time according to regulations ICH Q7 and 21
CFR
211 and internal procedures
- Support/initiate analytical test results initial investigation on the floor
- Reviews and may approve manufacturing analytical testing on the floor
- Uses analytical skills to help ensure shop floor compliance to internal standards and procedures
- Draft and review Standard Operating Procedures
- Perform other duties as assigned and take ownership to support the implementation of activities needed including but not limited to facility start-up and continuous operations.
- A Bachelor's or Master's degree in a relevant discipline (e.g., microbiology, chemistry, biological sciences, bioengineering, etc.).
- 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 facilities, drug substance preferred
- Batch record review, housekeeping monitoring, GMP document review and/or creation.
- Reviewing deviation reports, change controls, CAPA, and analytical data.
- Experience with Data Integrity
- Knowledge of and experience in GMP, following applicable regulations, or willingness to become GMP proficient.
- Authorization to work in the United States indefinitely without restrictions or sponsorship.
Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Sanford, NC are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options.
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Seniority levelMid-Senior level
Employment typeFull-time
Job functionProduction
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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