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Chloé Fattebert is a Quality Affairs Manager at Neurosoft Bioelectronics. Chloé has over eight years of experience in quality assurance and regulatory affairs for medical devices and IVDs. Prior to their current position, they served as a director of quality assurance and regulatory affairs for Produits Dentaires SA, where they were responsible for PRRC and management representative for the company. Chloé has also held a position as a QA/RA senior associate & team leader for Medidee Services SA, where they were responsible for regulatory & clinical affairs, quality management for medical devices & IVDs, ISO 13485, MDR, IVDR, internal audit of QMS, supplier audit, PMS, vigilance, CAPA, complaint handling, and team leader for the on-boarding of new people joining the company.

Chloé Fattebert has a Master of Advanced Studies in Medical Devices Regulatory Affairs and Quality Assurance from the University of Bern. Chloé also has a Bachelor of Science in Microtechniques from HEIG-VD. Chloé has a high school diploma in Biology and Chemistry from Gymnase de Marcelin. Chloé is also certified as an Internal & Supplier Auditor for ISO 13485/ISO 9001 from Medidee.

They are on a team with Benoît Huguet - Process Engineer, Olivia Molloy - Process Engineer, and Margaux Roulet - R&D Engineer. Chloé Fattebert reports to Nicolas Vachicouras, CEO & Co-Founder.