Analytical Chemistry Data Reviewer

Google Chrome Microsoft Edge Apple Safari Mozilla Firefox Analytical Chemistry Data ReviewerFull-time Compensation: USD 26.25 - USD 30.00 - hourlyCompany DescriptionAt Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees. Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.Job DescriptionThe 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 ResponsibilitiesGMP Data & Documentation ReviewReview 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 ResolutionCollaborate 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 & ComplianceConduct laboratory safety and compliance walkthroughs and document observations as requiredComplete all required safety, procedural, and refresher trainings on scheduleQualificationsEducation & ExperienceBachelor’s degree in Chemistry, Life Sciences, or a related scientific field2+ years of cGMP experience in a regulated laboratory environmentTechnical SkillsHands-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 RequirementsAble to meet physical requirements, including lifting 25 lbs., prolonged standing or walking, pushing/pulling equipment, and bending or reaching for suppliesAdditional RequirementsAbility 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 sponsorshipAdditional InformationPosition 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 applyExcellent full-time...