Clinical Affairs Specialist (m/w/d)

The location specified in the vacancy (Aschau, Erfurt or remote) is discussed based on where the candidate lives. Initial training lasts 6 weeks and is held at the main site.

Your tasks
  • Planning and performing clinical assessments
  • Creating clinical evaluation reports
  • Planning and supporting the PMS and PMCF activities
  • Planning and monitoring for clinical studies on new products
  • Creating PMS reports (including PSUR) and safety report (SSCP)
  • Supporting activities in Risk Management
Your requirements
  • Degree in medical technology, industrial engineering, product engineering or a comparable qualification
  • Experience in the field of regulatory or clinical affairs is welcomed
  • Knowledge of the regulations governing medical technology
  • Strong customer orientation
  • Pragmatic and analytical approach
  • Self-assured, good manners and assertive
  • Good organisational skills, flexibility and resilience
  • Highly motivated and flexible team player
We offer

As a reliable employer we support our Königsee team with a host of prospects and flexible offers for all phases in life. Discover us:

  • A structured and detailed initiation at the company sites where a mentor will support you
  • Varied and responsible tasks including decision pathways and a flat hierarchy
  • A future-proof and permanent job in a growing company
  • A family-oriented and social personnel policy, incorporating flexible working hours, for instance, ensures a healthy work-life balance
  • Sustainability and responsibility for future generations is incorporated into the day-to-day running of the business
  • Open company structure
  • Free parking
  • Water dispensers
  • Monthly vouchers
  • Company pension … And much more … And much more


Please email your applications with your salary expectations electronically only to Ms Höpping-Schwenk:


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