Additionalinformation

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.

Companydescription

Company Description

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries, helping to make life and our environment safer, healthier, and more sustainable. From the food we eat and the water we drink to the medicines we rely on, Eurofins laboratories work with some of the world's largest companies to ensure products are safe, authentic, and accurately labeled.

Jobdescription

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.