AustCorp Executive is seeking a Senior Quality & Regulatory Affairs Specialist to drive regulatory activities for innovative orthopaedic medical devices. The role combines hands-on EU MDR work with collaboration across engineering and product teams in a hybrid Sydney setting.
Ideal candidates will have proven medical device regulatory experience, EU MDR expertise, and familiarity with ISO 13485. The position offers a permanent full-time arrangement with part time flexibility and a hybrid work
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📌 Regulatory Affairs Lead (Sydney)
🏢 Austcorp
📍 Sydney
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