Novo Nordisk
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The Regulatory Affairs & PV Coordinator will support compliance with regulatory submissions, assist with Good Manufacturing Practice clearances, and ensure timely responses to safety reports. Key responsibilities include managing regulatory inboxes, quality control of safety information, and contributing to training development.
As a Senior Regulatory Affairs Associate, you will lead regulatory activities for products in Australia and New Zealand, ensuring compliance and developing strategies for product registration and commercialization. You will manage regulatory submissions, liaise with regulatory authorities, and maintain accurate records while collaborating with cross-functional teams throughout the product lifecycle.