Head of Regulatory Affairs
Sartorius Stedim Biotech GmbH, Germany
Jennifer Neff, DVM, PhD, MBA, (RAC)
Director QM / RA & Medical Affairs
bess AG
Dr. Neff has worked in the areas of medical devices, pharmaceuticals and biotechnology for over 16 years, joining Sartorius Stedim Biotech GmbH in September 2020. Sartorius Stedim Biotech is a leading partner of the biopharma industry. The solutions are supporting customers to produce drugs safely, timely and economically. The key product categories of our company are cell cultivation, fermentation, filtration, purification, and fluid management.
Sartorius Stedim Biotech has a worldwide presence, with manufacturing, sales and R&D sites in more than 20 countries in Europe, North America and Asia.
Previously, she held Regulatory Affairs and Clinical Affairs positions at bess AG, Bayer Health Care, PAREXEL Consulting, NOXXON Pharma AG, Berlin Heart GmbH, and Biotronik GmbH & Co KG. Her experiences include a broad range of medical devices e.g. tracheobronchial stents, medical devices for “ENT” (ear, nose, throat), ventricular assist devices, devices for cardiovascular and endovascular diseases, tumor markers, and surgical instruments as well as different types of pharmaceuticals e.g. biomarkers, talc, cancer treatment. Prior to joining the industry Dr. Neff worked as a veterinarian in small and large animal practice as well as for the Primate Genetics division of the German Primate Center.
Dr. Neff received her PhD from the University of Veterinary Medicine of Hannover, her MBA from FOM – University of Applied Science, Germany, and holds a Regulatory Affairs Certification (RAC). She has published articles in primate genetics and is the Vice Chair of the European Council of RAPS (Regulatory Affairs Professional Society).
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