KOELIS
Corentin Bellee is an experienced regulatory affairs professional currently serving as the Regulatory Affairs Manager at KOELIS since July 2021. Prior to this role, Corentin worked as a Regulatory Affairs Specialist at Zimmer Biomet from July 2017 to July 2021, where responsibilities included leading regulatory actions for the implementation of Medical Device Regulations and overseeing external resources in CE marking for various classes of orthopedic medical devices. Earlier experience includes serving as Regulatory Affairs Project Manager at AMPLITUDE, focusing on CE marking for orthopedic devices and participating in product development, and as a Junior Project Manager at LISI Medical, involved in the development of cemented femoral stems. Corentin holds an Engineer's degree in Biological Engineering from Université de Technologie de Compiègne and a DUT in Physical Measurements from IUT de Caen, along with a Baccalauréat in Scientific studies from Lycée Jean Rostand Caen.