Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries. Driven by a commitment to innovation, we continuously strive to enhance access to medicines and improve patient care, creating better health outcomes for millions around the world.
Post : Executive - Regulatory & Business Continuity
Job Description
1. Preparation of registration strategy for Brazil submission
2. Adequate understanding on respective authority guidance and filing of new product and post approval changes
3. Review of documents related to product registration and dossier submission leading to faster approval
4. Prepare response to deficiency letter received from Anvisa, Brazil
5. Maintain life-cycle (PCH) / post approval changes for drug product registration dossiers including timely circulation of approval information
6. Provide regulatory support to cross functional department
7. Adequate assessment of change control as per regulatory guidance
8. Prepare and submit scientific advice to Anvisa, Brazil
Additional Information
Experience : 1-2 years
Qualification : M.Pharm
Location : Tandalja - R&D
Industry Type : Pharma/ Healthcare/ Clinical research
Business Unit : R&D1 Regulatory Affairs
End Date : 30th January 2026
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