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.
Positive knowledge of regulatory documentation and submission processes.
Valuable 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