Attend Sun Pharma’s walk-in interview on 13th July 2025 for Regulatory Affairs roles in Baroda & Halol. Join India’s No.1 pharma company in USFDA-approved facilities.
🚨 Sun Pharma Walk-In Drive for Regulatory Affairs Roles | Baroda & Halol | 13th July 2025
Sun Pharmaceutical Industries Ltd., India’s leading pharmaceutical giant and the world’s 4th largest specialty generics company, is conducting a walk-in interview on Sunday, July 13, 2025, for Regulatory Affairs roles at its Baroda and Halol facilities. This is an incredible opportunity for professionals looking to work in USFDA-regulated environments and contribute to regulatory operations across global markets.
🌟 Why Work at Sun Pharma?
With operations in over 100 countries and 43 manufacturing sites across five continents, Sun Pharma is a name synonymous with excellence, compliance, and innovation. The company focuses on therapies like oncology, dermatology, cardiology, and more, and offers a robust platform for career advancement in Regulatory Affairs.
📌 Walk-In Interview Details
- 🗓️ Date: Sunday, 13th July 2025
- ⏰ Time: 9:30 AM – 1:00 PM
- 📍 Venue:
Sun Pharmaceutical Industries Ltd., Sun Pharma Road, Tandalja, Baroda, Gujarat – 390012 - 📨 Email (for those unable to attend): HR.Tandalja@sunpharma.com
(Use subject: APPLICATION FOR REGULATORY AFFAIRS [ROLE])
🧪 Open Positions & Requirements
1. Regulatory Affairs – US (Baroda)
- Qualification: M.Pharm
- Experience: 2–7 years
- Grade: Executive / Senior Executive
- Responsibilities:
- Dossier compilation for US, EU, AU, Canada, and IL
- Query response handling
- Lifecycle management
- Skills: Knowledge of USFDA, EMA, TGA, Health Canada, and eCTD submissions
2. Regulatory Affairs – US (Labeling) (Baroda)
- Qualification: B.Pharm / M.Pharm
- Experience: 2–6 years
- Grade: Senior Officer / Executive
- Responsibilities:
- ANDA/NDA labeling per USFDA
- SPL generation and compliance
- Labeling query responses
- Skills: Expertise in SPL, drug listing, and USFDA labeling compliance
3. Regulatory Affairs – Plant (Halol)
- Qualification: M.Pharm
- Experience: 3–9 years
- Grade: Executive / Senior Executive
- Responsibilities:
- New product registration, variation filing
- QMS impact analysis, change control
- Coordination with plant and corporate RA
- Skills: Experience in QMS (CAPA, deviations, change control) and emerging markets
📄 Documents to Bring
- Updated resume
- Last 3 months’ salary slips
- Latest appointment/increment letter
- Educational certificates (B.Pharm/M.Pharm)
- Passport-size photo
- Aadhaar Card
🔍 Candidate Preferences
Sun Pharma is seeking candidates with a strong foundation in regulatory compliance, preferably from USFDA-inspected pharma environments. Hands-on experience in dossier preparation, labeling compliance, and QMS processes will be given priority.
💼 Why Choose a Career in Regulatory Affairs?
Regulatory Affairs professionals play a pivotal role in ensuring safe and effective global access to medicines. At Sun Pharma, you’ll work with international health authorities and contribute to lifesaving therapies through compliant submissions, lifecycle management, and regulatory strategy.
🧬 About Sun Pharmaceutical Industries Ltd.
Founded by Dilip Shanghvi in 1983, Sun Pharma has grown into a global powerhouse with revenues exceeding USD 5.8 billion. With more than 3,000 scientists, the company focuses on complex generics, biosimilars, and specialty medicines. Its Baroda and Halol plants are core hubs for regulatory and manufacturing excellence.
✅ How to Apply
If you’re unable to attend in person, email your resume to:
📧 HR.Tandalja@sunpharma.com
Mention your preferred role and clearly state your current CTC, expected salary, and notice period.
🚫 Disclaimer
Sun Pharma does not charge candidates at any recruitment stage. Beware of fraudulent calls or emails. Always verify via www.sunpharma.com
If you’re ready to accelerate your career in pharma regulatory affairs, don’t miss this opportunity to join India’s No.1 pharmaceutical brand. Attend the walk-in on 13th July 2025, or apply online today.
