Senior Analytical Chemistry Data Reviewer

Company DescriptionThe work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier, and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical, and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.

Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!

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 timelinesCommunication & 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 field4-5 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 dataProfessional SkillsStrong computer literacy and organizational skillsExcellent written and verbal communication with high attention to detailDemonstrated professionalism, integrity, and strong work ethicWork Style & Physical RequirementsAbility 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 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 InformationWhat 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 $36 -$40, depending on education and experience Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.