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Sun Pharma Hiring in Regulatory Affairs & Biotech | 0 – 4 Years

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M.Pharm, MSc in Biotechnology /Biochemistry /Lifesciences

Baroda

0 - 4 Years

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Sun Pharmaceutical Industries Ltd has announced multiple Executive-level openings in Regulatory Affairs (IRA) and Biotechnology (R&D) at its Baroda (Vadodara) facility. These roles are ideal for M.Pharm, MSc Biotechnology, Biochemistry, and Life Sciences graduates, offering strong exposure to drug regulatory submissions, biosimilar analysis, and GLP-compliant research environments.

If you’re targeting a career in regulatory affairs jobs in India or biotech R&D jobs for freshers, this opportunity aligns with current industry demand.


🔍 Job Overview

Company: Sun Pharmaceutical Industries Ltd
Location: Baroda (Vadodara), Gujarat
Department: R&D – Regulatory Affairs
Job Level: Executive (G12A)
Employment Type: Full-Time
Total Openings: 2 Roles

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🧪 Role 1: Executive – Regulatory Affairs (India)

Key Responsibilities

  • Evaluate regulatory strategies for Indian market submissions
  • Compile and submit dossiers to CDSCO HQ/Zonal offices
  • Handle CT, BE studies, and manufacturing approvals
  • Manage import/export regulatory permissions (Form 8, CT-17, etc.)
  • Coordinate CMC documentation review with cross-functional teams
  • Prepare IPC dossiers and support lab submissions
  • Handle post-approval changes and Phase IV clinical trial filings
  • Review and approve product label artworks

Eligibility Criteria

  • Qualification: M.Pharm
  • Experience: Minimum 3 years in regulatory affairs
  • Strong knowledge of CDSCO regulations and submission portals

🧬 Role 2: Executive – Biotechnology (Biosimilars)

Key Responsibilities

  • Develop and validate HPLC-based methods for proteins & peptides
  • Perform impurity profiling (HCP, HCD, leachables)
  • Work on advanced techniques like RP-HPLC, SEC-HPLC, CEX, N-Glycan
  • Design analytical strategies for biosimilar characterization
  • Prepare MDR, MQR, ATP reports
  • Ensure compliance with GLP standards
  • Support regulatory submissions with technical documentation

Eligibility Criteria

  • Qualification: MSc in Biotechnology / Biochemistry / Life Sciences
  • Experience: 0–4 years (freshers eligible)
  • Strong analytical and lab skills in biopharmaceuticals

💰 Salary & Benefits

  • Estimated Salary Range: ₹4.5 LPA – ₹9 LPA (based on experience)
  • Exposure to regulated pharma & biosimilar pipeline projects
  • Career growth in regulatory affairs and biotech R&D
  • Work in a GLP-compliant, innovation-driven environment
  • Collaborative culture focused on continuous learning

🚀 Why This Opportunity Matters

With increasing demand for biosimilars and regulatory compliance in India, roles like these provide:

  • Hands-on experience with CDSCO submissions
  • Entry into high-growth domains like biologics & regulatory science
  • Strong foundation for careers in RA, QA, clinical research, and biotech R&D

📩 How to Apply

Application Link For Executive – Regulatory Affairs (India)

Application Link For Executive – Biotechnology (Biosimilars)

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