Active Implantables Auditor & Product Specialist for Technical Documentation (combination role)

- Independent planning and implementation of conformity assessment procedures as well as audits for active implants of customers located around the world
- Client manager for global manufacturers of highly innovative medical devices
- Reliable processing of all customer orders and inquiries
- Management of projects with an international team
- Ensuring the transparency of the individual project phases and compliance with the Project deadlines
- participation in development tasks within the department and the area (process development)

- Successfully completed studies in physics, computer science or engineering, e.g. B. Medical technology, electrical engineering or mechanical engineering
- At least four years of professional experience in the field of implantable medical devices or external defibrillators
- In-depth experience in quality management, development, regulatory affairs (product approval) or product management of medical devices
- Careful working methods and empathy in contact with customers on an international level and in the team
- Creative, solution-oriented and innovative personality with an interest in activities for the further development of the department
- Fluent German and English skills
- Routine handling of MS Office applications