CMC Regulatory Lead: Vaccines Submissions & Strategy

GSK is seeking a senior CMC Regulatory Affairs leader to drive planning and delivery of CMC submissions across multiple markets. You will coordinate cross-functional inputs from QA, supply chain, manufacturing and external partners to ensure submission-ready documentation and timely regulatory milestones.

You will act as SME for CMC regulatory affairs, mentor team members, and lead process improvements to regulatory tools and templates, shaping regulatory strategy and lifecycle management.