Atomo Diagnostics Limited is seeking an experienced Regulatory Affairs Specialist to join our Sydney team on a full time, six-month fixed-term contract to support regulatory compliance and market access for in-vitro diagnostic (IVD) products across global markets, with focus on EU IVDR and Australian Therapeutic Goods Regulations.
This hands-on role collaborates with cross-functional teams through the product lifecycle, from development and regulatory submissions through to post-market
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📌 IVD Regulatory Lead — Global Submissions & Compliance (Sydney)
🏢 Atomo Diagnostics
📍 Sydney
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