Manager Clinical & Regulatory Affairs Software (m/w/d)
Meierhofer AGLeipzig, Saxony, Germany • Munich, Bavaria, Germany • Berlin, Germany • Hanover, Lower Saxony, Germany
Posted December 11, 2025
Full Time
About the Company
We are a family-owned company developing software solutions for clinics in Germany, Austria, and Switzerland, supporting people to improve patient health.
Job Description
We are looking for a Manager Clinical & Regulatory Affairs Software to strengthen our Quality Management Team at one of our locations in Leipzig, Berlin, Hannover, Munich, or in Home Office. You will be responsible for planning, compiling, and maintaining technical documentation of our medical products and updating clinical evaluations.
Requirements
- Completed study in a natural scientific field (e.g. medicine/pharmacy)
- In-depth experience in the creation of clinical evaluations according to MDR
- In-depth professional experience in the field of certification of software as a medical product (EU) and QM systems
- Very good knowledge in the field of medical processes, software as a medical product, and medical technology
- Very good German and English knowledge in word and writing
Benefits
- Mobile work at up to 3 days a week
- Sabbaticals
- Onboarding and mentoring program
- Good working atmosphere and strong team cohesion
- Bicycle leasing and public transport subsidy
- Meierhofer Academy