Registration Specialist

Updated: March 12, 2024 12:16 PM GMT

Full-time Job in Virum, Capital Region of Denmark

Phillips-Medisize

Virum

Your Job

Are you interested in being part of a team responsible for regulatory submission, approval, and registration of medical devices and combination products worldwide?

Are you interested in working in a challenging regulatory environment at the interface between device and drug regulations, and willing to expand your regulatory expertise?

Are you interested in developing your skills and competencies for global Medical Device registrations?

Then you may be the person we are looking for to join our growing team in Phillips-Medisize’s Global Innovation & Development Center based in Virum and Struer.

Our Team

We are a team of RA specialists working on approving drug delivery devices/combination products globally and maintaining registrations. We are engaged in development projects and work directly with pharma clients to get devices registered globally. Together we follow global changes in regulations, and we actively build our competencies to meet demand for global... More Detail