Regulatory Affairs Professional

Job Requirements Your tasks and responsibilities:

• Analyzing global requirements for product registration and support the creating, shaping, and maintaining process framework for the implementation of the necessary activities in the pre- and post-market phases

· Planning and preparing product related medical device submissions with Siemens Healthineers internal regional units according to country specific regulatory requirements and maintaining of licensed products (e.g., for India, Latin America, Asia)

• Take responsibility for component registrations following respective standards such as BIS, CCC and NOM of relevant parts of the Siemens Healthineers AT products
• You will provide professional advice to and actively support internal departments, such as product management, (clinical) marketing- and product development in implementation and fulfillment of global regulatory requirements (laws, guidelines, regulations) for registration of medical devices