GMP Data Review Associate

Eurofins•Columbia, MO

3d•Onsite

About The Position

Eurofins BPT-Columbia is hiring an entry-level GMP Data Review Associate for its Quality Assurance team in Columbia, Missouri. This role is suited to 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 reviews scientific data and laboratory reports to help ensure they meet quality and regulatory standards before final release, and supports report review and approval in collaboration with laboratory operations teams. The position is full-time, onsite, and first shift, 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.
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 environment.
Positive attitude, adaptability, and willingness to learn GMP regulations and quality systems.

Nice To Haves

Laboratory experience gained through coursework, internships, research, or employment.

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 to support final report review and approval processes.
Perform additional duties as assigned.