Carole Viennot

Carole Viennot has extensive experience in regulatory affairs and analytical development within the biomedical and pharmaceutical sectors. Currently employed at NORAKER as a Regulatory Affairs professional since February 2015, Carole is responsible for updating CE marking files, ISO 13485 audits, and product registrations for exports. Prior to this role, Carole served as an Analytical Development Scientist and later as a team leader at Patheon, managing GMP analyses and project follow-ups for drug products. Experience includes contributions at Johnson & Johnson in the Analytical Development Department and internships at Givaudan, AstraZeneca, Huntsman, Technisurface, and Air Liquide. Carole holds a Master's degree in Regulatory Affairs in Medical Devices from Université Claude Bernard Lyon 1 and a Master's degree in Chemistry from CPE Lyon.