Study Manager Biosafety Testing

Eurofins BioPharma Product Testing Leiden B.V., part of the globally operating Eurofins Scientific network, is a leading GMP-certified contract laboratory serving the (bio)pharmaceutical industry. Based at the Leiden Bio Science Park, we provide a comprehensive range of microbiological, viral, chemical, and physical quality control testing for pharmaceutical raw materials, intermediates, and finished products. In addition to our standard test packages, we develop and validate productspecific methods in close collaboration with our clients, and we also offer smallscale manufacturing services. We have a professional team consisting of a mix of young and experienced people with different backgrounds and experiences. Together we strengthen global healthcare and help advance the pharmaceutical product quality and patient safety worldwide. As a Study Manager at Eurofins BPT Leiden B.V., you play a central scientific role in ensuring that studies are designed, executed, and documented to the highest quality standards. You translate customer inquiries into clear and robust study protocols and are responsible for preparing well‑structured study reports. A key part of your work involves reviewing and interpreting test results, identifying deviations, and coordinating troubleshooting when necessary. You collaborate closely with the laboratory team and provide scientific guidance and practical support to ensure that each study is executed correctly, consistently, and in accordance with relevant guidelines and quality standards. You explain procedures and advise analysts during study execution. Throughout the study, you communicate with customers on scientific content, progress, and outcomes, and you coordinate internally with laboratory staff regarding methods, results, and any corrective actions required. You also help address exceptions and technical issues, ensuring proper documentation and compliance with internal and external requirements. You work closely with colleagues