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About the Role
Position Summary
You will lead CMC regulatory activities to support product registrations and lifecycle maintenance in the Philippines. You will work closely with colleagues across regulatory, quality, supply and project teams to prepare clear, compliant dossiers and respond to agency questions. We value people who are careful, curious and collaborative. This role offers strong growth, meaningful impact on patient access, and the chance to develop global regulatory expertise while helping GSK unite science, technology and talent to get ahead of disease together.
Responsibilities
- Prepare CMC sections for regulatory dossiers, variations, renewals and responses to regulatory agency questions.
- Review technical data and ensure submissions are complete, accurate and ready for filing.
- Work with manufacturing, quality, supply and local regulatory teams to meet submission timelines.
- Monitor local regulatory changes and apply ...
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