- Acting as a subject matter expert for medical device software
- Creation and maintenance of technical documentation and the design history file
- Writing change requests
- Management of changes in the software – as well as in the production environment and the product life cycle management
- Software verification and validation in accordance with the Regulatory Affairs department
- Working together with external developers
- Software development according to IEC 62304 Standard


- Minimum 5 years of experience in software development in the medical device industry (preferably with Risk Class II / III products)
- MSc. or equivalent degree in Software Engineering
- Experience in firmware development in C/C++ and application development in C#, as well as code review
- Background in software design and software release management
- Proficient with Integrated Development Environments
- Previous experience with build servers and test platforms
- Strong English communication skills both verbally and in writing, good command of German preferred