QA Data Review Associate

Are you a detail-oriented science graduate who enjoys reviewing data ensuring accuracy and maintaining quality standards Join Eurofins as a

QA Data Review Associate

where youll 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 youll review laboratory reports scientific data protocols and quality records to ensure accuracy completeness traceability and compliance with established procedures and regulatory requirements. Youll 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. What Youll Do 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. Qualifications : Required Qualifications Bachelors 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. Ideal Candidates Will Have 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. Additional Information : Position is full-time position Monday - Friday 8:00am - 4:30pm. Candidates currently living within a commutable distance of Columbia MO are encouraged to apply. 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 Build a career where quality matters. If youre ready to apply your scientific background in a role that supports regulatory excellence and continuous improvement we encourage you to apply today. Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer. Remote Work : No Employment Type : Full-time