Jobannonce: Risk Manager / RA Specialist for Medical Device Development
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RSP Systems A/S, Odense
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.