Eurofins
GMP Data Review Associate
Columbia, MO, United States · On-site · Posted 2026-11-05
Job Description 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.
Qualifications 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.
Additional Information 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.
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