GMP Data Review Associate

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.