Sun Pharma Hiring Executive – Regulatory Affairs (India)

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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.

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