Job Description
Healthcare Professionals Group, a global medical device organisation, has a contract opportunity for a Regulatory Affairs qualified to support submissions, technical documentation, and lifecycle regulatory activities across markets.
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You will collaborate with global Regulatory Affairs and cross-functional teams to ensure compliance with TGA, EU MDR and international regulations, and contribute to post‐market surveillance, CAPA and labeling reviews across projects.
📌 Global Regulatory Affairs Specialist - Medical Devices (New South Wales)
🏢 Healthcare Professionals Group
📍 New South Wales
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