Emmanuelle E.

Emmanuelle E. is a Regulatory Affairs Specialist with extensive experience in the pharmaceutical and biotech industries. Currently at TRB Chemedica International SA since July 2019, Emmanuelle represents the Regulatory Affairs team in complex global projects and leads cross-functional Chemistry Manufacturing & Controls (CMC) meetings. Prior experience includes serving as an International CMC Regulatory Affairs Specialist at BD, where Emmanuelle managed CMC strategies for submissions and life cycle management across international markets. Emmanuelle has a strong foundation in regulatory strategies, having previously held roles at Labatec Pharma SA and other companies as a Chemist Analyst, contributing to quality assurance and analytical functions. Emmanuelle holds a Technology University Degree in Chemistry from Université Joseph Fourier and has completed various certifications in pharmaceutical training and first aid, enhancing professional skills in regulatory affairs and healthcare practices.