At a Glance
- Tasks: Lead CMC submissions and strategy for vaccines across multiple markets.
- Company: Join GSK, a global leader in healthcare innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on mentorship and process improvement.
- Why this job: Make a real difference in vaccine development and regulatory processes.
- Qualifications: Experience in CMC regulatory affairs and strong leadership skills.
The predicted salary is between 60000 - 80000 £ per year.
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.
We think you need these skills to ace CMC Regulatory Lead: Vaccines Submissions & Strategy
CMC Regulatory Affairs
Submission Planning
Cross-Functional Coordination
Quality Assurance (QA)
Supply Chain Management
Manufacturing Processes
Regulatory Documentation
