Proclinical Group is seeking a Senior Regulatory Affairs Associate to lead global regulatory compliance and product registrations for medical devices. You will shape regulatory strategy, manage the regulatory lifecycle, and mentor teammates while collaborating with cross-functional teams to drive business success.
The role requires expertise in FDA, EU MDR, TGA, Health Canada, and related standards, with a focus on accuracy, risk assessment, and timely submissions in a fast-paced workplace.
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📌 Global Regulatory Lead for Medical Devices (Melbourne)
🏢 Proclinical Group
📍 Melbourne
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