Global Regulatory Affairs Specialist (IVD)

A leading medical diagnostics firm based in Milan is seeking a Regulatory Affairs Specialist to join their team. The ideal candidate will have a Scientific Degree and at least 3-4 years of experience in the Medical Device/IVD sector. Responsibilities include defining regulatory strategies for global market access, preparing necessary documentation for product registration, and monitoring applicable regulations. This full-time role offers significant opportunities for growth within the organization.
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