Global Regulatory Affairs Portfolio Lead, Marketed Products, Radiopharma

Role: Lead regulatory oversight and lifecycle management for a portfolio of Pharmaceutical Diagnostics radiopharmaceuticals, ensuring compliance, registration, and strategic regulatory guidance. Responsibilities: manage all regulatory activities including variations, renewals, and commitments; provide strategic input for commercial planning; liaise with regional and global regulatory stakeholders; optimize portfolio through external environment assessment; support agency meetings; oversee regulatory information systems; influence regulatory outcomes through stakeholder engagement. Requirements: Bachelor's in Life Sciences, Pharmacy, Chemistry or related field; extensive experience in Regulatory Affairs with post-approval lifecycle expertise; proven success working with global regulatory agencies and cross-functional teams; strong communication and project management skills. Preferred: experience in radiopharmaceuticals, digital and AI-driven regulatory strategies. High-Value: biologics or small molecules within radiopharmaceuticals, post-approval lifecycle management, global regulatory interface, strategic portfolio optimization. Work Setup: not specified; location likely hybrid or onsite based on organizational context.