Job Description

We are looking for our future Advanced Regulatory Affairs Specialist to join our Regulatory team in Italy, GB or Sweden.

Let's talk about the role:

As part of the EMEA Regulatory Affairs team, participate to all regulatory activities related to the import and distribution of ResMed products in EMEA region from product registrations to follow-up of product changes and post-market activities. Work on European processes together with other functions to ensure the overall compliance of ResMed activities in EMEA. Work at the interface between the legal manufacturer and the country partners to ensure proper coordination.

Finally, as part of the implementation of the new European regulation on medical devices, activities related to the control/registration of products placed on the European market are planned.

Let's talk about key responsibilities:

  • Collaborate to the evaluation of regulatory requirements, preparation, planning, su...

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