Location
lisboa
Job Type
Full-time
Posted
July 09, 2026

Job Description

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 su...

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