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. 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 Qualifications. Education & Experience. Bachelor’s degree in Chemistry, Life Sciences, or a related scientific field 4-5 years of cGMP experience in a regulated laboratory environment. Technical Skills. Hands-on experience with HPLC/ UPLC and UV-Vis spectrophotometry. Experience with ELISA, MCE, and/or i. CIEF preferred. Proven ability to process and review quantitative liquid chromatography data. Professional Skills. Strong computer literacy and organizational skills. Excellent written and verbal communication with high attention to detail. Demonstrated professionalism, integrity, and strong work ethic. Work Style & Physical Requirements. Ability to work independently and collaboratively in a team environment. Self-motivated, adaptable, and comfortable in a fast-paced setting. 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 Additional Information. What to Expect in the Hiring Process: 10-15 Minute Phone Interview with Region Recruiter 45-60 Minute Virtual Interview with Manager and/or Group Leader 30 Minute Virtual Interview with Site Director Additional Details: This is a full-time, onsite position based on a first-shift schedule (Monday–Friday, 8:30 am – 4:30 pm), 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 options. Life and disability insurance 401(k) with company match. Paid vacation and holidays. Hourly rate is between $36 -$40, depending on education and experience Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran