GMP Data Review Associate
About The Position
Eurofins BPT-Columbia is seeking an entry-level GMP Data Review Associate to join its Quality Assurance team in Columbia, Missouri. The role is intended for recent graduates and early-career scientists interested in quality systems, regulatory compliance, and scientific documentation in a GMP-regulated laboratory environment. It is not a data science position. The associate ensures scientific data and laboratory reports meet quality and regulatory standards before final release. The position works with laboratory operations teams and supports final report review and approval processes. This is a full-time, onsite, first-shift position, Monday through Friday, 8:00 AM to 4:30 PM. Candidates must live within a reasonable commuting distance of Columbia, Missouri.
Requirements
- 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.
- Laboratory experience gained through coursework, internships, research, or employment.
- Strong attention to detail and 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 and collaborate effectively within a team.
- Positive attitude, adaptability, and willingness to learn GMP regulations and quality systems.
- Ability to reside within a reasonable commuting distance of Columbia, Missouri, for consistent onsite work.
Responsibilities
- Review laboratory data packages and scientific reports for 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 with laboratory operations teams while supporting final report review and approval processes.
- Perform additional duties as assigned.
Benefits
- Comprehensive medical coverage
- Dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
