This role is responsible for the coordination and execution of Post Market Surveillance activities aligned with global regulations with a focus on the EU Medical Device Regulation (MDR). The position is to be located in Frankfurt cm Main, Germany.
Our clients are global leaders in high-end eyewear including design, production and distribution of sunglasses and optical frames for prestigious brands. Their manufacturing combines expert know-how with the essential values of each brand, thus creating frames of exceptional quality.
How to apply