Global Regulatory Affairs Portfolio Lead, Marketed Products, Radiopharma

Role: Senior Regulatory Affairs leader managing the registration and lifecycle of Pharmaceutical Diagnostics - Radiopharmaceuticals products. Objectives include ensuring compliance, strategic regulatory guidance, and supporting approvals to optimize product portfolios. Responsibilities: oversee all regulatory activities (variations, renewals, commitments), provide strategic input to commercial plans, coordinate with regional and global stakeholders, lead agency interactions, and maintain regulatory systems. Requirements: Bachelor's in Life Sciences, Pharmacy, Chemistry or related; extensive experience in Regulatory Affairs with emphasis on post-approval lifecycle management; proven cross-functional and global agency collaboration skills; strong communication and project management ability. Preferred: experience in radiopharmaceuticals sector, familiarity with digital and AI tools, and regulatory expertise in radiopharmaceuticals. High-Value: focus on radiopharmaceutical product lifecycle, international regulatory strategy, regional coordination, and global compliance. Work setup: not specified, but involvement in global and regional regulatory networks implies potential international engagement.