About this role
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 proceduresVerify logbook and documentation entries for accuracy, completeness, and adherence to GDP standardsConfirm the sample chain of custody throughout the testing lifecycleReview audit trails to ensure actions align with procedural requirements and timelinesCross-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 correctionsPartner with laboratory teams to support compliance and continuous improvement initiativesGood Documentation Practices (GDP)
Accurately document activities in logbooks, notebooks, and electronic systems following GDP expectationsSafety & Compliance
Conduct laboratory safety and compliance walkthroughs and document observations as requiredComplete all required safety, procedural, and refresher trainings on schedule Education & Experience
Bachelor’s degree in Chemistry, Life Sciences, or a related scientific field2+ years of cGMP experience in a regulated laboratory environmentDirect experience reviewing GMP data in an industrial settingTechnical Skills
Hands-on experience with HPLC/UPLC and UV‑Vis spectrophotometryExperience with ELISA, MCE, and/or iCIEF preferredProven ability to process and review quantitative liquid chromatography dataPhysical Requirements
Able to meet physical requirements, including lifting 25 lbs., prolonged standing or walking, pushing/pulling equipment, and bending or reaching for suppliesAdditional Requirements
Ability to learn new processes and manage multiple tasks simultaneouslyAbility to follow instructions and comply with company policies and regulatory requirementsAuthorized 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 optionsDental & Vision: Full dental and vision coverage availableLife & Disability Insurance: Employer-sponsored plansRetirement: 401(k) plan with company matchPaid Time Off: Vacation days, paid holidays, and additional PTO optionsCompensation: $26.25 - $30.00 per hour
LinkedIn: #LI-EB1
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.