Marion Calvet

CMC Regulatory Affairs Manager at EUSA Pharma

Marion Calvet is an experienced CMC Regulatory Affairs Manager currently at EUSA Pharma since January 2021, focusing on biologics and responsible for updating M3, managing change controls, and coordinating global strategies for new registrations. Prior to this, Marion served as a Regulatory Affairs Manager at ProductLife Group, overseeing regulatory life-cycle management for drugs. Marion's experience also includes roles as a Regulatory Affairs Consultant at CaduCeum, API Purchasing Technical Specialist at Mylan, and Technical Customer Service Representative at GATTEFOSSÉ, all emphasizing regulatory compliance and quality management. Education includes a Master's degree in Pharmacy from IUP santé, faculté de Pharmacie, completed in 2015.

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EUSA Pharma

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We are committed to transforming the lives of people affected by cancer or rare disease, globally. We continuously strive to uncover opportunities which address gaps across adult and paediatric care. Helping the people with few or no options available is at the heart of everything we do. EUSA Pharma is part of Recordati Rare Diseases (recordatirarediseases.com), the business unit dedicated to rare disease in the Recordati group. Recordati has a total staff of more than 4,300, dedicated to the research, development, manufacturing and marketing of pharmaceuticals. More information can be found in the press release: https://www.recordati.com/resources/Pubblicazione/___58a6bc05f57c4861aae203c930cd1682_/eusa-closing-pr.pdf We see a need. We work together. We don’t give up.