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.
#J-18808-Ljbffr
📌 Senior Regulatory Affairs Lead, MedTech & AI Software (Sydney)
🏢 Enovis
📍 Sydney
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.