Apply now at Cadila Pharmaceuticals, Dholka Plant – Openings for Regulatory Affairs Managers with 11–25 years of experience. M.Pharm required. Email your CV today.
📢 Cadila Pharmaceuticals Hiring Regulatory Affairs Managers – Apply Now!
Are you an experienced Regulatory Affairs (RA) professional seeking a senior position in the pharmaceutical industry? Cadila Pharmaceuticals Ltd. invites qualified professionals to join its RA Department at the Dholka Plant, Ahmedabad.
This is a golden opportunity to work with one of India’s leading pharmaceutical companies, known for its commitment to innovation, quality, and compliance.
🧪 Position Details:
- Designation: Manager to General Manager – Regulatory Affairs
- Experience: 11 to 25 Years
- Qualification: M. Pharma
- Location: Dholka, Ahmedabad, Gujarat
✅ Key Responsibilities:
- Handle licenses: Manufacturing, Wholesale, FSSAI
- Coordinate with State FDAs (Gujarat, Jammu, Rajasthan) for COPPs, FSCs, and product permissions
- Manage submissions to Zonal CDSCO (Ahmedabad)
- Oversee WHO GMP inclusion and inspections
- Handle CT-10/MA applications and GMP audits
- Work with CDL Kasauli/NIB for testing and method transfers
- Manage NCB/CBN: Import/Export licenses, compliance, and returns
- Respond to regulatory complaints and represent the company in hearings
- Approve change controls, deviations, and product artworks
🎯 Ideal Candidate Profile:
- Strong knowledge of Gujarat FDA and CDSCO (Zonal & Central)
- Proficient in Gujarati language (mandatory)
- Experienced with regulatory portals:
- Gujarat FDA Portal
- SUGAM
- NSWS
- CBN/NCB
- CDL Kasauli
📩 How to Apply:
Send your updated CV to: savitri.thakor@cadilapharma.com
