Jennifer George is focusing on Quality & Regulatory Affairs in bioscience, specifically on the implementation of the new IVD Regulation (EU) 2017/746 (IVDR).
Before joining Kalms Consulting, she worked for more than ten years in international research facilities and in the biotechnological industry. She has profound experience in the implementation and monitoring of quality management systems.
Additionally, Jennifer has expertise in the field of medical devices that are subject to regulatory approval and market authorization in Europe.
She holds a diploma in Biotechnology. Jennifer is a native speaker in German and fluent in English. Additionally, she has considerable knowledge of French.