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Sun Pharma Hiring: Executive – RA & FRD Non Orals | Apply Now!

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Sun Pharmaceutical Industries Ltd, Indiaโ€™s leading pharmaceutical company, has announced two new openings in its R&D division at Baroda (Tandalja). The positionsโ€”Executive – Regulatory Affairs (RA) and Executive – FRD Non Oralsโ€”offer an excellent opportunity for skilled M.Pharm professionals to grow in one of the countryโ€™s most reputed pharma organizations.

If you are passionate about drug development, regulatory submissions, and formulation innovation, this is your chance to build a thriving career with Sun Pharmaโ€™s cutting-edge research teams.


๐Ÿ’ผ 1. Position: Executive โ€“ Regulatory and Business Continuity (RA)

๐Ÿ“ Location: Baroda (Tandalja – R&D)
๐Ÿงช Business Unit: R&D1 Regulatory Affairs
๐ŸŽ“ Qualification: M.Pharm
๐Ÿ’ผ Experience: 2โ€“5 years
๐Ÿ•“ Job Grade: G12A

Key Responsibilities

  • Collaborate with Product Development and cross-functional teams to ensure timely regulatory input for new drug formulations.
  • Review and approve regulatory documents; prepare and submit high-quality dossiers for faster approvals.
  • Manage lifecycle activities such as annual reports, renewals, and variation submissions.
  • Ensure compliance with regulatory decisions and maintain product documentation in central repositories.
  • Participate in self-development activities and stay updated with evolving global guidelines.

โš—๏ธ 2. Position: Executive โ€“ FRD Non Orals

๐Ÿ“ Location: Baroda (Tandalja – R&D)
๐Ÿงช Business Unit: R&D1 Regulatory Affairs
๐ŸŽ“ Qualification: M.Pharm
๐Ÿ’ผ Experience: 1โ€“3 years
๐Ÿ•“ Job Grade: G12A

Key Responsibilities

  • Design and conduct experiments for non-oral dosage forms (Microsphere, Implant, In-situ-gel, etc.) using QbD principles.
  • Execute Design of Experiments (DoE) and analyze data using MINITAB.
  • Prepare development protocols, product reports, and technology transfer documents.
  • Conduct scale-up batches, prepare regulatory documents (Form 29, CPD for DCGI), and ensure compliance.
  • Coordinate with ADD, RA, and manufacturing units for project-related activities.

๐ŸŽฏ Required Qualifications

  • Degree: Master of Pharmacy (M.Pharm)
  • Experience: 1โ€“5 years depending on the role
  • Skills:
    • Strong understanding of regulatory guidelines (US/EU/DCGI)
    • Knowledge of formulation development and QbD approach
    • Excellent communication and documentation abilities
    • Proficiency in data analysis tools like MINITAB

๐ŸŒŸ Why Join Sun Pharma?

At Sun Pharma, employees are empowered to โ€œCreate their own sunshine.โ€ The company fosters continuous learning, professional growth, and teamwork across all departments.
Youโ€™ll gain:

  • Opportunities for professional development
  • A collaborative R&D environment
  • Exposure to global regulatory processes
  • Industry-leading benefits and wellness programs

๐Ÿ“ How to Apply

Application Link For Executive โ€“ Regulatory and Business Continuity (RA)

Application Link For Executive โ€“ FRD Non Orals

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