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🚨 We’re Hiring – Apply Now!
Function: India Regulatory Affairs
Experience: 2–8 Years
Qualification: M.Pharm
Location: Vadodara
Key Responsibilities:
- Evaluate regulatory strategies for products intended for registration in India
- Review CMC and other supporting documents for regulatory submissions
- Review CT/BE documentation for regulatory applications
- Compile and prepare regulatory submission dossiers
- Review product artworks and prepare Product Information (PI)
- Evaluate and submit applications through the online portal to obtain domestic manufacturing and marketing approvals from DCGI
📧 How to Apply:
Send your updated resume to Rosemary.varghese@sunpharma.com
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