Head - Regulatory Affairs

Head - Regulatory Affairs (Emerging Markets & Europe)

What You'll Do:

- Lead regulatory submissions & approvals with agencies (EMA, ANVISA, TGA, SFDA, etc.)

- Define regulatory strategies for new launches and lifecycle management

- Drive in-licensing & out-licensing due diligence to support business growth

- Ensure compliance with EU & EM regulations, staying ahead of evolving requirements

- Mentor and manage a global regulatory team, working cross-functionally with R&D, Clinical, QA, Commercial & BD

What Were Looking For:

- 16+years of Regulatory Affairs experience (pharma/biotech/medical devices)

- Strong exposure to EU & Emerging Market submissions

- Hands-on experience in licensing due diligence & authority interactions

- Proven leadership and people management track record.