Stéphane Bellec

Stéphane Bellec has extensive work experience in regulatory affairs and quality assurance in the pharmaceutical industry. Stéphane began their career as a Pharmacist in 1995 before joining the Marine Nationale as an Officer Cadet, where they conducted analytical chemistry assays and developed a method to detect heavy metals in seawater. Stéphane then worked at Servier as a Clinical QA Project Leader and later became a Project Lead in Worldwide Regulatory Affairs. Bellec then joined TRIO - Translational Research in Oncology, where they served as the Director of Quality Assurance & Regulatory Affairs, overseeing regulatory intelligence, audits, vendor qualification, and team management. Stéphane most recently worked at LFB, first as the Manager of Regulatory Strategy and Development and then as the Head of the Clinical-Regulatory Strategy and Labelling Unit in the Regulatory Affairs Group. Bellec's work experience spans over 25 years, highlighting their expertise in regulatory strategy and quality management.

Stéphane Bellec earned a Doctor of Pharmacy degree from Université Paris Cité in the field of pharmaceutical sciences in 1996. Additionally, they obtained a Master's degree in Quality Management Systems applied to Drugs (known as DESS) from the same university, specializing in pharmaceutical sciences in 1997.