Jennifer George is a Senior Consultant for Quality & Regulatory Affairs with over a decade of experience in the medical device industry. She specializes in regulatory-compliant product development and has extensive expertise in implementing and monitoring quality and risk management systems in accordance with ISO 13485 and ISO 14971. Jennifer is well-versed in European regulatory frameworks, including IVDD/IVDR and MDD/MDR, and serves as a Qualified Person Responsible for Regulatory Compliance (PRRC). Prior to joining Kalms Consulting, she worked in international research institutions and the biotechnology and MedTech sector. She holds a diploma in Biotechnology and brings more than 15 years of project management experience. A native German speaker, Jennifer is fluent in English and possesses solid knowledge of French.
