Chloé holds a BSc in Microengineering from the HES-SO, and has gained significant experience over the past 8 years working in the Medical Device Industry. As a QA/RA consultant, she specialized in audits, regulatory strategy, manufacturing processes, product quality management, and QMS implementation for novel medical devices, including active implantables. She later worked as QA/RA Director in the endodontic field, leading the team in charge of MDR transition, quality & regulatory strategy, product portfolio optimization, device worldwide registration, and Technical Documentation.

Welcome to the team, Chloé!