Florian Grimm

Florian Grimm is a seasoned professional in quality management and regulatory affairs, currently serving as the Quality Management Representative for Medical Devices and the Person Responsible for Regulatory Requirements (MDR) at Beiersdorf since October 2013. Prior to this role, Florian held the position of Regulatory Affairs Manager at DMG Dental-Material Gesellschaft mbH from October 2007 to September 2013. Florian Grimm holds a Diplom-Biologe degree in general biology from the University of Bremen, earned between 2001 and 2006.