From my educational background I am biologist. I have completed my PhD at the Helmholtz Research Centre of Munich in cooperation with the Technical University of Munich in the field of toxicology.
After that I gained several years of experience in the pharmaceutical industry with a focus on quality management.
Since nearly 4 years, I am working within TÜV SÜD in the sector of Medical Health Services. Currently, I am leading a team of experts and auditors for non-active medical devices and I am responsible for the Article 117 business in the regions DACH & Nordics.
Besides these roles, I am Auditor and Senior Product Specialist for non-active medical devices.