Karine Frimat

Karine Frimat is an experienced professional in the field of regulatory affairs, currently serving as Associate Director of CMC Regulatory Affairs (Biopharm) at GSK since April 2025. With a career that spans over two decades, Karine has held significant positions including Senior Regulatory Consultant (CMC) at DLRC Regulatory Consultancy, Regulatory Affairs CMC Manager - Biologics at Amgen, and Senior Manager of CMC, Global Regulatory Affairs at Eisai EMEA. Previous roles also include senior and foundational positions at Gilead Sciences, Teva Pharmaceuticals, and GlaxoSmithKline, among others. Karine holds a PhD in Organic Chemistry from the University of Bath and has a solid background in regulatory affairs beginning with a Development Chemist role at Exchem.