Regulatory Affairs Manager (m/f/d)

In your role as a specialist (m/w/d) for new medical devices, you work closely with the development department and product management You develop the admission requirements and strategies for our medical devices, primarily in the EU and the USA You check the technical documentation and create additional documents within the scope of the approvals and modifications You analyse the relevant rules together with the specialist departments and derive appropriate measures You maintain regulatory databases In addition, you represent the company to the notified body

You have completed their studies in medical technology or comparable training, ideally in connection with additional training to regulatory content You provide sound knowledge of regulatory requirements in the field of product approval and technical documentation Ideally, you already have professional experience and experience with medical devices, but also ambitious career starters (m/w/d) give us a chance In addition to a targeted and structured way of working, you can convince by knowledge in project management In addition, your personality is characterized by communication and organizational skills as well as independent thinking and acting Our strong internationalisation also requires reliable English skills

Guests can enjoy a future-proof workstation at a modern location with an attractive remuneration. As a family-friendly company, we value that you can combine your professional and private goals and feel comfortable in the company. In addition to flexible working time, we support this through a wide range of social services, healthy placement and events outside the working day. .