Stefan Menzl has more than 20 years of experience as senior leader in the healthcare industry.
In his current role as Principal Consultant for the Qservegroup, he provides strategic and hands-on support in the areas of Regulatory, Quality and Clinical to the medical device industry.
He most recently served as Global Vice President Quality & Regulatory Affairs for Paul Hartmann AG. Before joining Paul Hartmann, he was responsible as functional leader for Quality, Regulatory, and Clinical in companies like Abbott, Advanced Medical Optics, Edwards Lifesciences and Baxter.
Besides his expertise in Regulatory, Clinical and Quality, he also gained experience as General Manger, leader of remote global teams and functional manager of mergers and acquisitions, spin-offs and integration of acquired companies
Stefan holds a Ph.D. in Biotechnology. He has been publishing numerous articles related to Quality- and Regulatory matters and a training book on CE marking in Europe.
He acts as subject matter expert and author for RAPS Education Development. Additionally, he has been lecturing ‘Regulatory Affairs EU & USA’ at the University of Pforzheim.