Laboratory Data Review Associate - On-site QA & Growth

Eurofins BioPharma Product Testing North America; Columbia Township (MO); Presencial; USD 40.000 - 55.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401(k) with company match

Paid holidays and vacation

Professional growth

Descripción de la vacante

Eurofins USA BioPharma Services in Columbia, MO, is seeking a Laboratory Data Review Associate to join the Quality Assurance team. This entry‑level role focuses on reviewing scientific reports, data, and documentation to ensure accuracy, GMP compliance, and regulatory alignment before final approval.

You will work with laboratory and quality staff, maintain records, support internal audits, and participate in continuous improvement initiatives.

Formación

• Bachelor's degree in a scientific discipline.
• Ability to work in the United States indefinitely without current or future sponsorship.

Responsabilidades

• Review laboratory reports and supporting documentation to verify accuracy, completeness, and GMP compliance.
• Ensure data is properly documented and meets standards before final approval.
• Collaborate with laboratory operations and quality personnel to resolve discrepancies.
• Assist with internal quality audits and quality system activities.
• Maintain records per SOPs.
• Support continuous improvement within QA.
• Perform related duties as assigned.

Conocimientos

Attention to detail

Written and verbal communication

Computers & common software

Multitasking

Independent and team work

Willingness to learn

Educación

Bachelor's degree (Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Chemical Engineering or related)

Descripción del empleo

Eurofins USA BioPharma Services in Columbia, MO, is seeking a Laboratory Data Review Associate to join the Quality Assurance team. This entry‑level role focuses on reviewing scientific reports, data, and documentation to ensure accuracy, GMP compliance, and regulatory alignment before final approval.

You will work with laboratory and quality staff, maintain records, support internal audits, and participate in continuous improvement initiatives.