QA Data Review Associate

Eurofins USA BioPharma Services • Columbia, MO

1d

About The Position

Eurofins is seeking a detail-oriented science graduate to review laboratory data and documentation that support the safety and quality of products. The QA Data Review Associate verifies laboratory reports, scientific data, protocols, and quality records for accuracy, completeness, traceability, and compliance with established procedures and regulatory requirements. The role works closely with laboratory and quality teams to identify and resolve discrepancies, support quality systems, and maintain client quality standards. It is an opportunity for recent graduates and early-career professionals to build a career in quality assurance, compliance, data review, or laboratory operations in the pharmaceutical and life sciences industry.

This is a full-time position, Monday through Friday, 8:00 a.m. to 4:30 p.m. Candidates living within a commutable distance of Columbia, Missouri, are encouraged to apply.

Requirements

• Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Science, Chemical Engineering, or a related scientific discipline.
• Ability to work in the United States without current or future sponsorship requirements.
• Strong attention to detail and organizational skills.
• Excellent written and verbal communication abilities.
• Ability to learn new processes quickly and manage multiple priorities in a fast-paced environment.

Nice To Haves

• An interest in quality systems, compliance, and regulated laboratory environments.
• Strong critical thinking and problem-solving skills.
• A collaborative mindset and a passion for producing high-quality work.

Responsibilities

• Review laboratory reports, data packages, and supporting documentation for accuracy, completeness, and compliance.
• Partner with scientific teams to identify, communicate, and resolve data discrepancies or quality concerns.
• Support quality system activities, including CAPA investigations, change controls, training records, and procedural updates.
• Review protocols, methods, reports, and SOPs for alignment with regulatory and client requirements.
• Evaluate corrective actions and assess potential compliance impacts.
• Communicate findings effectively with laboratory personnel and clients when needed.
• Monitor quality metrics and contribute to continuous improvement efforts.
• Maintain a strong commitment to safety, accuracy, and regulatory compliance.
• Perform additional quality-related responsibilities as assigned.

Benefits

• Comprehensive medical coverage
• Dental options
• Vision options
• Life insurance
• Disability insurance
• 401(k) with company match
• Paid vacation
• Paid holidays

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level