Analytical Sciences Data Review Group Leader

Google Chrome Microsoft Edge Apple Safari Mozilla Firefox Analytical Sciences Data Review Group LeaderFull-time Compensation: USD 28.50 - USD 34.75 - hourlyCompany DescriptionThe work we do at Eurofins matters, and so do our employees. At Eurofins, 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.If you’re looking for a rewarding career, apply with us today!  Job DescriptionWe are seeking a driven and detail-oriented Analytical Sciences Data Review Group Leader to support GMP laboratory operations. This role combines hands-on data review responsibilities with team leadership, ensuring high-quality, compliant analytical data while mentoring and developing a high-performing team.The ideal candidate brings strong cGMP experience, a deep understanding of analytical techniques, and a proactive leadership style focused on quality, accountability, and continuous improvement.This is a Data Review role, nor a Data Engineering role Key ResponsibilitiesData Review & ComplianceReview GMP analytical data for accuracy, completeness, and compliance with governing proceduresVerify logbook entries for completeness and correctnessConfirm chain of custody integrity for all tested samplesReview audit trails to ensure proper execution and adherence to procedural timelinesCommunicate efficiently with laboratory personnel to resolve discrepancies, annotations, and correctionsApply Good Documentation Practices (GDP) in all records, including logbooks, notebooks, and electronic systemsPerform laboratory safety and compliance walkthroughs and document observationsComplete all required safety and procedural trainingsLeadership & Team ManagementLead, manage, and develop a team of data reviewersCoordinate team workload and ensure timely completion of deliverablesManage cross-training initiatives and team capacity planningTrack, monitor, and report productivity and quality metricsServe as a proactive and effective point of contact for client and internal teamsConduct routine safety walkthroughs and employee compliance checksParticipate in hiring, onboarding, and training of new team membersDeliver training programs for new hires and existing staffSupport scheduling needs, including overtime and weekend coverage as requiredQualificationsBS in Chemistry or related field2+ years of cGMP experience + 2+ years of leadershipExperience with HPLC/UPLC, UV-Vis, and LC data analysisExposure to ELISA, MCE, or iCIEFStrong communication, organization, and attention to detailHigh integrity with a focus on data quality and complianceAbility to multitask in a fast-paced environment and work independently or on a teamAble to lift 25 lbs and stand/walk for extended periodsMust be authorized to work in the U.S. 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...