On-Site Lab Data Review Associate — QA & Compliance

Eurofins BioPharma Product Testing North America; Columbia Township (MO); Vor Ort; USD 45.000 - 60.000; Vollzeit

Benefits dieser Stelle

Comprehensive medical, dental, and vis

Life and disability insurance

401(k) with company match

Paid holidays and vacation time

Opportunities for professional growth

Zusammenfassung

Eurofins USA BioPharma Services in Columbia, MO seeks a Data Review Associate to join our Quality Assurance team. This on-site role focuses on reviewing laboratory data packages, reports, and documentation to ensure GMP/GLP compliance before final release.

The ideal candidate holds a bachelor's in a scientific field and has detail-oriented, collaborative skills. Recent science graduates are encouraged to apply; relocation assistance is not offered.

Qualifikationen

• Bachelor's degree in a related scientific field.
• Experience or exposure to regulated laboratory environments preferred.
• Strong attention to detail and communication skills.
• Familiarity with GMP/GLP and SOPs is desirable.

Aufgaben

• Perform detailed reviews of laboratory data packages, worksheets, reports, notebooks, and supporting documentation for accuracy and compliance.
• Verify that testing records and calculations comply with GMP/GLP and client requirements.
• Identify discrepancies and collaborate with staff to resolve issues within required timelines.
• Maintain data integrity and support timely reporting of results.
• Assist with internal audits and continuous improvement initiatives.

Kenntnisse

Laboratory experience

Quality assurance

Quality control

Regulatory compliance

Documentation review

Attention to detail

Ausbildung

Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Chemical Engineering, Microbiology, or related field

Tools

Microsoft Office

Electronic documentation systems

Jobbeschreibung

Eurofins USA BioPharma Services in Columbia, MO seeks a Data Review Associate to join our Quality Assurance team. This on-site role focuses on reviewing laboratory data packages, reports, and documentation to ensure GMP/GLP compliance before final release.

The ideal candidate holds a bachelor's in a scientific field and has detail-oriented, collaborative skills. Recent science graduates are encouraged to apply; relocation assistance is not offered.