Key Requirements:
- Minimum 2 years of experience in Regulatory Affairs
- Hands-on experience in dossier preparation for African countries
- Knowledge of CTD, ACTD & eCTD dossier compilation
- Experience in product registration, variations, renewals, and query handling
- Good understanding of pharmaceutical regulatory guidelines
- Excellent documentation and communication skills
- B.Pharm / M.Pharm required
Responsibilities:
- Prepare and compile regulatory dossiers for export markets
- Handle product registration submissions
- Respond to regulatory authority queries
- Manage variations, renewals, and amendments
- Ensure regulatory compliance for international markets
- Maintain regulatory documentation and records
Contact: +91 79905 81394
Pay: ₹11,000.00 - ₹40,000.00 per month
Benefits:
- Versatile schedule
- Paid sick time
- Paid time off
Education:
- Bachelor's (preferred)
Experience:
- Regulatory Affairs Executive: 1 year (preferred)