• Evaluate the suitability of new/altered technical components used for the manufacture of medical devices

• Connect and collaborate with various internal functions as well as external partners to develop the best change strategy

• Plan, coordinate and prioritise various changes and their processing in order to ensure continuous and compliant manufacturing


• Technical degree ideally in electrical or mechanical engineering or a similar discipline

• Experience in the development of class 3 medical devices, ideally AIMDs

• Independent, detail-oriented and cross-functional working style

• Very good communication skills in English, both written and spoken, German is a plus