EBOS Group invites applications for a 12-month contract in post-market vigilance within the ANZ medical device portfolio. You will support day-to-day regulatory activities, maintain regulatory records, and work with Regulatory, Quality, Commercial, and Supply Chain teams to meet obligations.
This role offers hands-on experience in post-market compliance and regulatory submissions, exposure to TGA IRIS reporting, licence management, and audit readiness across Australia and Recent Zealand.
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📌 Post-Market Regulatory Associate – ANZ Medical Devices (Ryde)
🏢 Ebos Group
📍 Ryde
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