Your mission
* You are responsible for identifying the regulatory requirements for approval in the region
* You develop and support approval strategies
* The provision of submission documents is one of your tasks
* You provide strategic input for the development of assigned projects
* You are the central point of contact for our subsidiaries and partners
* Advising and monitoring normative requirements in the development process
* You will be responsible for the implementation of internal company training courses
* You are responsible for informing stakeholders about approval changes, standards and their impact on our products at an early stage
Your talents
* Completed scientific/technical studies or comparable training
* Experience in the field of medical device approval
* Initial expertise in the field of medical devices
* Confident appearance in global project structures
* Communicative and analytical skills
* Independent and structured way of working
* Very good knowledge of German and English