Groupe ProductLife is seeking a Regulatory Affairs Officer / Associate Consultant based in Australia to support regulatory activities across Australia, Current Zealand, and the JAPAC region. You will help with submissions, registrations, lifecycle maintenance, and regulatory interactions with authorities such as the TGA and Medsafe.
The role requires an undergraduate qualification in pharmaceutical sciences and at least three years of relevant regulatory/quality experience, with strong communication
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📌 Regulatory Affairs Specialist APAC Submissions & Lifecycle (Australia)
🏢 Groupe ProductLife
📍 Australia
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