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: bewerbung@koenigsee-implantate.de
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