Group Leader- Data Review

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Data Review & Compliance Review GMP 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 Ability to direct and monitor work assigned to team members. Understanding of regulatory requirements. Communicate effectively with staff and members of other departments. BS in chemistry, biology, biochemistry or related field 2+ years of cGMP experience and 2+ years of leadership 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. indefinitely without sponsorship Working schedule will be  Full-Time, Second Shift, M-F 12pm-8pm.  Candidates  currently living within a commutable distance of Columbia, MO  are encouraged to apply. No relocation assistance will be given. 25% travel may be required. This position is  NOT  remote.  Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.