Sun Pharmaceutical Industries Ltd, India’s largest pharmaceutical company, has announced two Executive-level openings in Regulatory Affairs at its Tandalja (Baroda) R&D facility. These roles are part of Sun Pharma’s R&D1 Regulatory Affairs business unit and offer strong exposure to global regulatory submissions, lifecycle management, and health authority interactions.
If you are an M.Pharm professional aiming to build or accelerate your career in Regulatory Affairs (RA) across US, EU, Brazil, Canada, and other international markets, this opportunity is highly relevant.
📌 Open Positions Overview
1️⃣ Executive – Regulatory & Business Continuity (RA EM)
- Location: Baroda (Tandalja – R&D)
- Experience: 1–2 years
- Focus Market: Brazil (ANVISA)
- Job Grade: G12A
2️⃣ Executive – Regulatory Affairs
- Location: Baroda (Tandalja – R&D)
- Experience: 3–6 years
- Focus Markets: US, EU, Australia, Canada, Israel & Palestine
- Job Grade: G12A
🧑💼 Key Responsibilities
Executive – Regulatory & Business Continuity
- Develop registration strategies for Brazil submissions
- Handle new product registrations and post-approval changes (PCH)
- Prepare and submit responses to ANVISA deficiency letters
- Manage lifecycle maintenance of regulatory dossiers
- Assess change control impacts as per regulatory guidelines
- Prepare and submit Scientific Advice requests to ANVISA
- Provide regulatory support to cross-functional teams
Executive – Regulatory Affairs
- Compile and review CTD/eCTD dossiers for US, EU, AU, Canada & Israel
- Manage query responses and submission timelines
- Perform lifecycle management activities for global markets
- Act as single point of contact for Israel & Palestine submissions
- Allocate projects and mentor regulatory associates
- Review documents from stakeholders for accuracy and compliance
🎓 Eligibility & Qualifications
- Education: M.Pharm (Mandatory)
- Experience:
- 1–2 years (Brazil / Emerging Markets – RA EM role)
- 3–6 years (US, EU & ROW markets – RA role)
- Key Skills:
- Regulatory dossier compilation
- Post-approval change management
- Health authority correspondence
- Strong understanding of global RA guidelines
💼 Why Join Sun Pharma?
At Sun Pharma, employees are encouraged to “Create Your Own Sunshine” by taking ownership of their careers and growing in a collaborative environment.
Benefits Include:
- Exposure to global regulatory markets
- Strong learning & career progression
- Supportive R&D ecosystem
- Competitive compensation & benefits
- Opportunity to work with India’s leading pharma innovator
💰 Estimated Salary (Indicative)
- ₹6,00,000 – ₹10,00,000 per annum
(Salary may vary based on experience, role, and interview performance)
📥 How to Apply?
Application Link For Executive – Regulatory & Business Continuity (RA EM)
Application Link For Executive – Regulatory Affairs
