Regulatory Professional

Opportunity summary

. Are you energised by coordinating regulatory submissions across a global product portfolio, ensuring that the right documentation reaches health authorities worldwide, on time and in full compliance? Do you thrive when navigating complex timelines, diverse stakeholders and ever-changing regulations? If so, this is your opportunity to play a central role in bringing innovative treatments to patients around the world. Your new role As a Regulatory Professional in Affiliate Coordination & Optimization (ACO), you will be at the heart of planning, coordinating and executing national registration file documentation, including pharmaceutical certificates and statements, for submissions to health authorities worldwide. You will act as the central point of contact for affiliates and headquarters stakeholders, keeping multiple submissions on track across overlapping and often challenging timelines. Key responsibilities include: Planning, coordinating and executing national registration file documentation for global regulatory submissions across the Novo Nordisk product portfolio Clarifying country-specific documentation needs with affiliates and assessing requirements a1 …

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