Tasks Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR) Preparing deficiency reports in case of non-conformities with the requirements of the MDR Serving as an internal point of contact for clinical matters as part of the interfaces with other internal departments, offering support and close exchange with colleagues Delivering high-quality reliable and predictable services within defined timelines Optionally providing support during audits of clinical processes of medical device manufacturers as a clinical expert (remote or on-site) Optionally continuing to practice medicine in part-time Qualifications Physician with completed medical degree Minimum of four years of clinical practice in health care services or related sectors in the area of General/Visceral surgery or (operative) Urology (preferably board-certification or equivalent) Two years of experience in usage, d...