Medical Device Compliance Specialist

4 days ago


Århus, Århus Kommune, Denmark Vitrolife Group Full time
Role Summary

We are looking for a Regulatory Affairs Specialist to join our team at the Vitrolife Group. The ideal candidate will have a strong background in regulatory affairs and experience working with medical devices.

In this role, you will be responsible for providing regulatory support to new product development projects and coordinating regulatory projects for existing registrations.

You will also have the opportunity to work on translational projects, evaluating regulatory intelligence and implementing changes to product design specifications.



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