Sun Pharmaceutical Industries Ltd, India’s leading pharmaceutical company, has announced two new openings in its R&D division at Baroda (Tandalja). The positions—Executive – Regulatory Affairs (RA) and Executive – FRD Non Orals—offer an excellent opportunity for skilled M.Pharm professionals to grow in one of the country’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 Pharma’s cutting-edge research teams.
💼 1. Position: Executive – Regulatory and Business Continuity (RA)
📍 Location: Baroda (Tandalja – R&D)
🧪 Business Unit: R&D1 Regulatory Affairs
🎓 Qualification: M.Pharm
💼 Experience: 2–5 years
🕓 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.
⚗️ 2. Position: Executive – FRD Non Orals
📍 Location: Baroda (Tandalja – R&D)
🧪 Business Unit: R&D1 Regulatory Affairs
🎓 Qualification: M.Pharm
💼 Experience: 1–3 years
🕓 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.
🎯 Required Qualifications
- Degree: Master of Pharmacy (M.Pharm)
- Experience: 1–5 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
🌟 Why Join Sun Pharma?
At Sun Pharma, employees are empowered to “Create their own sunshine.” The company fosters continuous learning, professional growth, and teamwork across all departments.
You’ll gain:
- Opportunities for professional development
- A collaborative R&D environment
- Exposure to global regulatory processes
- Industry-leading benefits and wellness programs
📝 How to Apply
Application Link For Executive – Regulatory and Business Continuity (RA)
Application Link For Executive – FRD Non Orals
