GMP Analytical Chemistry Data Reviewer

The  Analytical Chemistry Data Reviewer  is responsible for reviewing GMP laboratory data and documentation to ensure compliance with established procedures, data integrity standards, and regulatory requirements. This role requires a strong chemistry background and experience reviewing analytical data in a GMP-regulated environment.

Key Responsibilities

GMP Data & Documentation Review

• 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 Cross-Training & Laboratory Support:

• May be required to participate in cross-training opportunities across laboratory testing functions to broaden technical knowledge and enhance operational flexibility.

• Develop and maintain proficiency in applicable analytical testing techniques and laboratory processes as assigned.

• May be required to provide occasional hands-on laboratory testing support during periods of increased workload, staffing needs, or business priorities, when qualified and appropriately trained.

• Collaborate with laboratory personnel to ensure timely completion of testing activities while maintaining compliance with GMP, GDP, safety, and regulatory requirements. Communication & Issue Resolution

• Collaborate with testing personnel to resolve data annotations, discrepancies, or corrections

• Partner with laboratory teams to support compliance and continuous improvement initiatives Good Documentation Practices (GDP)

• Accurately document activities in logbooks, notebooks, and electronic systems following GDP expectations Safety & Compliance

• Conduct laboratory safety and compliance walkthroughs and document observations as required

• Complete all required safety, procedural, and refresher trainings on schedule Education & Experience

• 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 Technical Skills

• Hands-on experience with  HPLC/UPLC  and  UV‑Vis spectrophotometry

• Experience with  ELISA, MCE, and/or iCIEF  preferred

• Proven ability to process and review quantitative liquid chromatography data Physical Requirements

• Able to meet physical requirements, including lifting 25 lbs., prolonged standing or walking, pushing/pulling equipment, and bending or reaching for supplies Additional Requirements

• Ability to learn new processes and manage multiple tasks simultaneously

• Ability to follow instructions and comply with company policies and regulatory requirements

• Authorized to work in the United States indefinitely without sponsorship Position is  Full Time, Monday-Friday, First Shift, Monday through Friday from 8am-4:30pm.  Candidates currently living within a commutable distance of  Rensselear, New York,  are encouraged to apply

Excellent full-time benefits include: 

• Medical Coverage:  Comprehensive medical insurance options
• Dental & Vision:  Full dental and vision coverage available
• Life & Disability Insurance:  Employer-sponsored plans
• Retirement:  401(k) plan with company match
• Paid Time Off:  Vacation days, paid holidays, and additional PTO options
• Compensation: $26.25 - $30.00 per hour   

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Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.