QA Data Review Associate

Eurofins•Columbia, MO

18h•Onsite

About The Position

Are you a detail-oriented science graduate who enjoys reviewing data, ensuring accuracy, and maintaining quality standards? Join Eurofns as a QA Data Review Associate, where you'll play a critical role in verifying laboratory data and documentation that supports the safety and quality of products used around the world. In this position, you'll review laboratory reports, scientific data, protocols, and quality records to ensure accuracy, completeness, traceability, and compliance with established procedures and regulatory requirements. You'll work closely with laboratory and quality teams to identify and resolve discrepancies, support quality systems such as CAPAs and change controls, and help maintain the high standards our clients expect. This is an excellent opportunity for recent graduates and early-career professionals seeking to build a career in quality assurance, compliance, data review, or laboratory operations within the pharmaceutical and life sciences industry.

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 to ensure 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.