Regulatory Project Manager - Devices
GSK plc(1 month ago)
About this role
The role manages CMC (Chemistry, Manufacturing and Controls) regulatory projects for a portfolio of medical devices and drug‑device combination products across global markets. The position works closely with supply, technical, quality and local operating companies and contributes to GSK’s mission by ensuring compliant regulatory filings and lifecycle management. It offers a visible impact and development opportunities within a large biopharma organisation.
Required Skills
- CMC Regulatory
- Regulatory Strategy
- Dossier Preparation
- Change Control
- Manufacturing
- Supply Chain
- Cross-functional Coordination
- Time Management
- Stakeholder Engagement
- Inspection Support
Qualifications
- Bachelor’s Degree in Pharmacy, Chemistry or Related
- Master’s Degree in Pharmacy, Chemistry or Related (Preferred)
- Regulatory Affairs Certification (Preferred)
About GSK plc
gsk.comAt GSK, we unite science, technology and talent to get ahead of disease together
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