Job ad: Risk Manager / RA Specialist for Medical Device Development

Risk Manager / RA Specialist for Medical Device Development

Join our dedicated team and become part of a company applying state-of-the-art technology that establishes an all-new category of glucose monitoring.

Do you want to be part of a team responsible for regulatory approval and registration of the world’s first truly non-invasive glucose monitoring device?

The Risk Manager / RA Specialist is expected to work within the QA/RA department and in close cooperation with our development team. As our Risk Manager / RA Specialist your tasks will include:

• Participate in the development and execution of regulatory strategies.
• Support the design and development team in identifying applicable regulatory requirements, standards, their impact and how to interpret them.
• Assemble regulatory submission package and support submission process.