GMP Analytical Chemistry Data Reviewer — Data Integrity

Eurofins; New York (NY); On-site; USD 36,000 - 41,000; Full time

Benefits offered by this job

Medical coverage

Dental & vision

401(k) plan

Paid time off

Job summary

Eurofins USA PSS Insourcing Solutions is seeking an Analytical Chemistry Data Reviewer to assess GMP laboratory data and documentation for regulatory compliance. A strong chemistry background with experience reviewing analytical data in GMP settings is required.

Responsibilities include GMP data review, logbook verification, chain of custody, audit trails, and collaboration with lab personnel to ensure timely, compliant testing.

Qualifications

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

Responsibilities

• Review GMP data generated by laboratory personnel to ensure compliance with approved procedures.
• Verify logbook and documentation entries for accuracy, completeness, and adherence to GDP standards.
• Confirm the sample chain of custody throughout the testing lifecycle.
• Review audit trails to ensure actions align with procedural requirements and timelines.
• Collaborate with laboratory personnel to ensure timely completion of testing activities while maintaining compliance with GMP, GDP, safety, and regulatory requirements.
• Collaborate with testing personnel to resolve data annotations, discrepancies, or corrections
• Partner with laboratory teams to support compliance and continuous improvement initiatives

Skills

GMP data review

Documentation review

Data integrity

Cross-functional collaboration

Education

Bachelor’s degree in Chemistry

Life Sciences degree

Tools

HPLC/UPLC

UV-Vis spectrophotometry

ELISA

Job description

Eurofins USA PSS Insourcing Solutions is seeking an Analytical Chemistry Data Reviewer to assess GMP laboratory data and documentation for regulatory compliance. A strong chemistry background with experience reviewing analytical data in GMP settings is required.

Responsibilities include GMP data review, logbook verification, chain of custody, audit trails, and collaboration with lab personnel to ensure timely, compliant testing.