- Prepare, review and submit regulatory documents including CTD, ACTD and variations.
- Ensure compliance with local and international regulatory requirements.
- Coordinate with internal teams and manufacturing clients.
- Maintain regulatory records, submissions and documentation.
- Support product registration, approvals and post-approval changes.
- Manage artwork approval processes for labels, packaging and promotional materials.
- Coordinate with internal teams for timely regulatory submissions and approvals.
Skills
- B.Pharm / M.Pharm or relevant qualification.
- 2+ years of experience in Pharmaceutical Regulatory Affairs.
- Good knowledge of regulatory documentation and submission processes.
- Good communication and coordination skills.
Pay: ₹240,000.00 - ₹540,000.00 per year
Benefits
- Cell phone reimbursement
- Adaptable schedule
- Paid sick time
- Paid time off
- Provident Fund