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Regulatory Affairs (India)
Sun Pharma
Baroda (R&D)
0–3 Years
Regulatory Affairs
CDSCO Submissions
₹3.5–6.5 LPA
🏢 About Sun Pharmaceutical Industries
Sun Pharma is one of the world’s leading pharmaceutical companies with a strong global presence. The R&D Regulatory Affairs division supports drug approvals and compliance within Indian regulatory frameworks.
📌 Job Overview
- Role: Executive – Regulatory Affairs (India)
- Location: Baroda (Tandalja – R&D)
- Qualification: M.Pharm
- Experience: Freshers or up to 3 years
- Department: R&D Regulatory Affairs
- Salary: ₹3.5 – ₹6.5 LPA (Estimated)
🔬 Core Responsibilities
- Evaluate regulatory strategies for India registrations
- Review CMC documents & coordinate with cross-functional teams
- Compile regulatory dossiers
- Submit applications to CDSCO HQ & zonal offices
- Handle CT & BE applications
- Manage import & marketing approvals
- Handle post-approval regulatory changes
- Verify label artwork & compliance requirements
📑 Regulatory Exposure Includes
- CDSCO portal submissions
- Clinical Trial & Bioequivalence permissions
- Import permissions & Form filings
- Phase IV & site approval applications
- IPC testing & regulatory documentation
🎓 Eligibility & Skills
- M.Pharm (Mandatory)
- Specialization in Regulatory Affairs / Pharmaceutics preferred
- Knowledge of CDSCO & Indian regulatory guidelines
- Strong documentation & compliance skills
- Attention to detail & regulatory accuracy
⭐ Why Join Sun Pharma?
- Strong entry into Indian Regulatory Affairs (IRA)
- Work in structured R&D regulatory environment
- Exposure to drug approval lifecycle
- Career growth in regulatory compliance & submissions
- Opportunity with one of India’s largest pharma companies
📌 Note Before You Apply:
Candidates interested in CDSCO submissions and Indian Regulatory Affairs will gain valuable domain expertise in this role.
Candidates interested in CDSCO submissions and Indian Regulatory Affairs will gain valuable domain expertise in this role.
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