$ cat jobs/analytical-science-data-review-group-leader-eurofins-2e93419e6c7d.json
Analytical Science Data Review Group Leader
At 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. 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, rather than 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 Co
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