28 Aug
|
Enovis
|
Queensland
Enovis Brisbane seeks an experienced Senior Regulatory Affairs Specialist to lead global regulatory strategies for orthopedic-enabled technologies, including SaMD.
You will develop submissions for US, EU and Australia and guide cross-functional teams to ensure compliant product launches.
Ideal candidates have 5+ years in medical devices, solid knowledge of ISO *********** and 510(k)/CE procedures, and a proven ability to manage regulatory activities across the product lifecycle while adapting
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📌 Senior Global Regulatory Affairs Lead, Medtech & Samd (Queensland)
🏢 Enovis
📍 Queensland