CMC Regulatory Affairs Lead – Biopharma Development

GSK is looking for a Senior Manager – CMC Regulatory Affairs to lead regulatory activities for development and commercial biopharmaceutical projects. This role involves driving CMC strategy, managing submissions, and mentoring teams. The ideal candidate will have substantial experience in drug development and regulatory compliance.

Located in Greater London, the position offers a chance to influence global regulatory processes and work in a dynamic environment focused on innovation. GSK emphasizes accountability, ambition for patients, and ethical practices.

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