Enovis is seeking a Regulatory Market Access Specialist to join the market access team. You will bring new and modified medical devices to market, ensuring ongoing compliance and preparing regulatory submissions for international markets.
You will support product development with regulatory input, maintain documentation for audits, and coordinate requirements across cross‐functional teams, leveraging Excel and PLM tools. English proficiency is essential.
📌 Global Medical Device Market Access Specialist (Italia)
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📍 Italia
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