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 timelinesCommunication & 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 field2–3 years of cGMP experience in a regulated laboratory environmentTechnical 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 dataProfessional Skills
Strong computer literacy and organizational skillsExcellent written and verbal communication with high attention to detailDemonstrated professionalism, integrity, and strong work ethicWork Style & Physical Requirements
Ability to work independently and collaboratively in a team environmentSelf‑motivated, adaptable, and comfortable in a fast‑paced settingAble 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 What to Expect in the Hiring Process:
10-15 Minute Phone Interview with Region Recruiter45-60 Minute Virtual Interview with Manager and/or Group Leader30 Minute Virtual Interview with Site Director Additional Details:
This is a full-time, onsite position based on a first-shift schedule (Monday–Friday, 8:30am – 4:30pm), with overtime required as needed. Candidates located within a commutable distance to Rensselaer, New York, are strongly encouraged to apply.
Excellent full-time benefits include:
Comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysHourly rate is between $26 -$33, depending on education and experience Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.