JAMP India Pharmaceuticals Pvt. Ltd. is a subsidiary of JAMP Pharma Group, a leading Canadian pharmaceutical company engaged in the development, manufacturing, and commercialization of high-quality generic and specialty medicines. With a strong presence in global regulated markets, JAMP India offers excellent career opportunities for regulatory affairs professionals to work on international pharmaceutical submissions. The company is conducting a walk-in interview for multiple Regulatory Affairs (CMC Canada & eCTD) positions at its Ahmedabad office.
Job Highlights
| Details | Information |
|---|---|
| Company | JAMP India Pharmaceuticals Pvt. Ltd. |
| Department | Regulatory Affairs |
| Job Location | Ahmedabad, Gujarat |
| Walk-in Date | Sunday, 5th July 2026 |
| Interview Time | 10:00 AM – 4:00 PM |
| Interview Venue | A-120/1, 12th Floor, Navratna Corporate Park, Ambli Bopal Road, Ambli, Ahmedabad – 380058 |
| Open Positions | 5 + 2 + 4 + 1 = 12 Positions |
Current Openings
| Role | Designation | Qualification | Experience |
|---|---|---|---|
| Regulatory Affairs – CMC Canada | Manager / Deputy Manager / Assistant Manager | M.Pharm / B.Pharm | 7–12 Years |
| Regulatory Affairs – CMC Canada | Senior Executive / Executive | M.Pharm / B.Pharm | 3–5 Years |
| Regulatory Affairs – CMC Canada | Assistant Manager | M.Pharm / B.Pharm | 7–9 Years |
| Regulatory Affairs – eCTD | Senior Officer / Officer / Trainee Officer | M.Pharm / B.Pharm | Freshers to 3 Years |
Market Exposure Required
- Canada (Mandatory)
- United States (US)
- Europe (EU)
- Australia
- New Zealand
Key Responsibilities
Regulatory Affairs – CMC Canada
- Review and finalize dossiers for drug submissions.
- Prepare and submit regulatory documents to Health Canada and other global authorities.
- Compile, review, and maintain CMC documentation.
- Coordinate with cross-functional teams during product development and lifecycle management.
- Ensure compliance with GMP and global regulatory guidelines.
- Handle post-approval changes, renewals, and variations.
Regulatory Affairs – eCTD
- Prepare, validate, and submit eCTD dossiers.
- Manage submission sequences and document lifecycle.
- Handle deficiency responses (Clarifications, SDN, NOD, NON).
- Perform publishing, validation, and maintenance of regulatory submissions.
- Ensure compliance with regulatory standards and submission timelines.
Eligibility Criteria
- Qualification: B.Pharm or M.Pharm.
- Relevant Regulatory Affairs experience for experienced roles.
- Freshers with internship experience in Regulatory Affairs are preferred for Trainee positions.
- Exposure to regulated markets, especially Canada, is mandatory for applicable roles.
Documents to Carry
- Updated Resume
- Passport-size Photograph
- Last Three Months’ Salary Slips
- Appointment Letter
- Latest Increment Letter (if applicable)
Important Instructions
- Candidates who have attended a JAMP India interview within the last 30 days are not eligible to apply.
- No registration fee or monetary payment is required during the recruitment process. Beware of fraudulent calls.
- Candidates unable to attend the walk-in interview can send their updated resume to hrindia@jamppharma.com or apply through the QR code provided in the official notification.
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