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GMP Data Review Associate @ Eurofins

Columbia, South Carolina, USOnsiteFull-timeJob reference REF82367M
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About this role

This is NOT a Data Science position.

Eurofins BPT-Columbia is seeking a GMP Data Review Associate to join our Quality Assurance team in Columbia, Missouri. This entry-level role is ideal for recent graduates and early-career scientists interested in quality systems, regulatory compliance, and scientific documentation within a GMP-regulated laboratory environment.

As a GMP Data Review Associate, you will play a critical role in ensuring scientific data and laboratory reports meet quality and regulatory standards before final release.

Key Responsibilities

  • Review laboratory data packages and scientific reports to ensure completeness, accuracy, and compliance with GMP and regulatory requirements.
  • Verify that reported results are supported by raw data and laboratory documentation.
  • Identify discrepancies, documentation issues, and potential compliance concerns and collaborate with laboratory personnel to resolve them.
  • Assist with internal quality audits and quality system activities.
  • Maintain accurate records and documentation in accordance with established procedures.
  • Work closely with laboratory operations teams while supporting final report review and approval processes.
  • Perform additional duties as assigned.

Ideal Candidate Profile

  • Laboratory experience gained through coursework, internships, research, or employment.
  • Strong attention to detail with the ability to identify errors, inconsistencies, and documentation gaps.
  • Excellent written and verbal communication skills.
  • Strong organizational and time-management abilities.
  • Proficiency with computer applications and scientific documentation.
  • Ability to work independently while collaborating effectively within a team environment.
  • Positive attitude, adaptability, and willingness to learn GMP regulations and quality systems.

Minimum Qualifications

  • Bachelor's degree in Chemistry, Biochemistry, Biology, Chemical Engineering, Pharmaceutical Sciences, or a related scientific discipline.
  • Authorization to work in the United States indefinitely without current or future sponsorship requirements.

This is a full-time, onsite, first-shift position working Monday through Friday, 8:00 AM to 4:30 PM. Candidates must reside within a reasonable commuting distance of Columbia, MO, as this role requires a consistent on-site presence.

What we Offer

  • 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

Take the first step toward a career in Quality Assurance and scientific data review.

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Skills

Testing & LaboratoryScienceAssociateBiotechnology

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