- 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.

- Valuable 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

- Flexible schedule

- Paid sick time

- Paid time off

- Provident Fund

Work Location: In person

📌 Regulatory Affairs Executive (Ahmedabad)
🏢 Sanjeevani Bio-tech Exim
📍 Ahmedabad