i‑Pharm Consulting is seeking a Regulatory Affairs Specialist to support IVD projects across the Asia-Pacific region, with a focus on IVDR transition. Reporting to the Regulatory Affairs Manager, you will coordinate regulatory submissions, manage changes, and maintain registrations with regional teams.
The role requires a Bachelor’s degree in science, at least two years in medical devices regulatory affairs, and robust collaboration across functions.
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📌 Apac Ivdr Regulatory Specialist Sydney
🏢 i-Pharm Consulting
📍 Sydney
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