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Pharmaceutical Manufacturing QA Associate

Job in Sanford, Lee County, North Carolina, 27330, USA
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
ADDITIONAL RESPONSIBILITIES
  • 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.
Qualifications
  • 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.
Additional Information

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 level

Mid-Senior level

Employment type

Full-time

Job function

Production

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Position Requirements
10+ Years work experience
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