GMP Data Reviewer: Analytical Chemistry & Data Integrity

Eurofins; New York; Presencial; USD 36.000 - 41.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Dental & Vision coverage

401(k) with company match

Paid time off

Descripción de la vacante

Eurofins USA PSS Insourcing Solutions is seeking an Analytical Chemistry Data Reviewer to review GMP laboratory data and documentation to ensure compliance with procedures, GDP standards, and regulatory requirements. A strong chemistry background and experience reviewing analytical data in a GMP environment are required.

The role involves GMP data review, documentation validation, and potential cross-training across laboratory testing functions.

Formación

• Bachelor’s degree in Chemistry, Life Sciences, or a related scientific field.
• 2+ years of cGMP experience in a regulated laboratory environment.
• Direct experience reviewing GMP data in an industrial setting.

Responsabilidades

• GMP Data & Documentation Review: verify data against procedures and GDP standards.
• Cross-Training & Laboratory Support: participate in cross-training and provide hands-on support when needed.
• Communication & Issue Resolution: resolve data annotations and discrepancies with teams.
• GDP & Good Documentation Practices: document activities following GDP expectations.
• Safety & Compliance: complete required trainings and maintain safety standards.

Conocimientos

GMP data review

Documentation

Analytical testing

Communication

Educación

BSc in Chemistry or Life Sciences

2+ years cGMP experience

Herramientas

HPLC/UPLC

UV-Vis spectrophotometry

ELISA

MCE

iCIEF

Descripción del empleo

Eurofins USA PSS Insourcing Solutions is seeking an Analytical Chemistry Data Reviewer to review GMP laboratory data and documentation to ensure compliance with procedures, GDP standards, and regulatory requirements. A strong chemistry background and experience reviewing analytical data in a GMP environment are required.

The role involves GMP data review, documentation validation, and potential cross-training across laboratory testing functions.