Director, CMC Regulatory Affairs

Position Summary
You will lead global Chemistry, Manufacturing and Controls (CMC) regulatory strategy for small molecule medicines. You will work closely with R&D, supply, quality and commercial colleagues to enable development, approval and uninterrupted supply. We value clear decision makers who build strong partnerships, solve problems with practical solutions, and support the growth of colleagues. This role offers visible impact, career growth, and the chance to help GSK unite science, technology and talent to get ahead of disease together.

Responsibilities

• Lead CMC regulatory strategy for investigational and early commercial small molecule medicines across global teams.
• Act as the CMC regulatory representative on cross-functional project and leadership teams.
• Identify regulatory risks and propose clear mitigation plans to senior leadership.
• Mentor and develop regulatory colleagues and, where required, manage a small team.
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