16 - 25 years
45 - 60 Lacs
Posted:1 week ago|
Platform:
On-site
Full Time
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 We're 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
Degree in Life Sciences/Pharmacy; advanced degree preferred
Jaca Technologies Private Limited
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