Experteer Italy seeks a Sr. International Regulatory Affairs Specialist to support regulatory submissions for IVD products in EMEA (non-EU).
You will collaborate with Global Regulatory Affairs to ensure timely registrations, renewals, and changes while building expertise in regulatory release processes and tracking tools. You will oversee partner licenses, registrations, and the regulatory change lifecycle, applying solid knowledge of IVD/medical device regulations and standards.
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📌 EMEA IVD Regulatory Lead — Global Submissions & Licensing (Milano)
🏢 Experteer Italy
📍 Milano
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