Analytical Sciences Data Review Group Leader

## Company Description **The 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 Description We 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 Responsibilities** **Data Review & Compliance** - Review GMP analytical data for accuracy, completeness, and compliance with governing procedures - Verify logbook entries for completeness and correctness - Confirm chain of custody integrity for all tested samples - Review audit trails to ensure proper execution and adherence to procedural timelines - Communicate efficiently with laboratory personnel to resolve discrepancies, annotations, and corrections - Apply Good Documentation Practices (GDP) in all records, including logbooks, notebooks, and electronic systems - Perform laboratory safety and compliance walkthroughs and document observations - Complete all required safety and procedural trainings **Leadership & Team Management** - Lead, manage, and develop a team of data reviewers - Coordinate team workload and ensure timely completion of deliverables - Manage cross-training initiatives and team capacity planning - Track, monitor, and report productivity and quality metrics - Serve as a proactive and effective point of contact for client and internal teams - Conduct routine safety walkthroughs and employee compliance checks - Participate in hiring, onboarding, and training of new team members - Deliver training programs for new hires and existing staff - Support scheduling needs, including overtime and weekend coverage as required ## Qualifications - BS in Chemistry or related field - 2+ years of cGMP experience + 2+ years of leadership - Experience with HPLC/UPLC, UV-Vis, and LC data analysis - Exposure to ELISA, MCE, or iCIEF - Strong communication, organization, and attention to detail - High integrity with a focus on data quality and compliance - Ability to multitask in a fast-paced environment and work independently or on a team - Able to lift 25 lbs and stand/walk for extended periods - Must be authorized to work in the U.S. 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…