BrickRed Systems is seeking an experienced Regulatory Affairs Contractor to support a global medical device portfolio from its NSW location. The role covers regulatory activities across the US, EU, and Australian markets, ensuring compliance with TGA, EU MDR, ISO 13485, ISO 14971, and 21 CFR 820.
You will prepare regulatory submissions, assess changes, and manage technical documentation, labeling reviews, and post-market surveillance while coordinating with cross-functional teams to ensure
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📌 Global Regulatory Affairs Lead - Medical Devices (Sydney)
🏢 BrickRed Systems
📍 Sydney
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