Enovis Corporation is seeking a Senior Regulatory Affairs Specialist to lead regulatory strategies for cutting-edge medical devices, software, and AI-enabled technologies.
You will manage submissions across the US, Europe, and Australia, collaborating with Engineering, Clinical, Quality, and Product teams to ensure compliant, market-ready solutions.
Ideal candidates bring 5+ years in medical devices, strong FDA/EU MDR knowledge, and experience with SaMD/AI.
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📌 Senior Regulatory Affairs Lead, Medtech & Ai Software (Sydney)
🏢 Enovis
📍 Sydney