JAMP India Pharmaceuticals Walk-In Drive 2026: Regulatory Affairs & eCTD Career Opportunities in Ahmedabad

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JAMP India Pharmaceuticals Announces Walk-In Recruitment Drive for Regulatory Affairs Professionals

Are you looking for a rewarding career in Regulatory Affairs within the pharmaceutical industry? JAMP India Pharmaceuticals Pvt. Ltd. is conducting a walk-in interview drive for experienced professionals and aspiring candidates interested in Regulatory Affairs (CMC) and eCTD submissions.

This recruitment drive offers excellent opportunities for candidates with expertise in global regulatory markets, dossier preparation, regulatory submissions, and electronic common technical document (eCTD) management. Professionals seeking career growth in highly regulated international markets such as Canada, Australia, New Zealand, Europe, and the United Kingdom are encouraged to participate.

📅 Walk-In Interview Schedule

Candidates interested in applying can attend the walk-in interview as per the details below:

  • Date: 5 July 2026 (Sunday)
  • Time: 10:00 AM to 4:00 PM
  • Venue: JAMP India Pharmaceuticals Pvt. Ltd., A-1207, 12th Floor, Navratna Corporate Park, Ambli Bopal Road, Ambli, Ahmedabad – 380058, Gujarat

💼 Available Job Positions

1. Regulatory Affairs – CMC Canada (Management Positions)

Designation:

  • Manager
  • Deputy Manager
  • Assistant Manager

Number of Openings: 2

Educational Qualification:

  • M.Pharm

Experience Required:

  • 7 to 12 years

Key Responsibilities:

  • Manage regulatory submissions for global markets.
  • Prepare and review Quality Overall Summaries (QOS).
  • Conduct portfolio due diligence activities.
  • Coordinate with international stakeholders and regulatory agencies.
  • Lead and mentor team members within the Regulatory Affairs department.
  • Support lifecycle management activities for pharmaceutical products.

2. Regulatory Affairs – CMC Canada (Executive Positions)

Designation:

  • Senior Executive
  • Executive

Number of Openings: 5

Educational Qualification:

  • B.Pharm / M.Pharm

Experience Required:

  • 7 to 9 years

Key Responsibilities:

  • Prepare and compile ANDS submissions.
  • Review CMC documentation for regulatory compliance.
  • Respond to deficiency letters and agency queries.
  • Coordinate submission activities for Canada and Australia.
  • Ensure compliance with regulatory guidelines and GMP requirements.

3. Regulatory Affairs – CMC Canada (Trainee Officer Positions)

Designation:

  • Trainee Officer

Number of Openings: 4

Educational Qualification:

  • B.Pharm / M.Pharm
  • Preference for Regulatory Affairs or Pharmaceutics specialization

Experience:

  • Freshers and candidates with relevant internships may be considered.

Key Responsibilities:

  • Assist in dossier compilation activities.
  • Support regulatory submission preparation.
  • Participate in regulatory documentation review.
  • Learn Health Canada regulatory requirements.
  • Coordinate with formulation and quality teams.

4. Regulatory Affairs – eCTD Submission Team

Designation:

  • Senior Officer
  • Officer
  • Trainee

Number of Openings: 1

Educational Qualification:

  • B.Pharm / M.Pharm

Experience Required:

  • 0 to 3 years

Key Responsibilities:

  • Prepare and validate eCTD submissions.
  • Manage Electronic Submission Gateway (ESG) activities.
  • Track regulatory submissions and supplements.
  • Handle lifecycle management for eCTD applications.
  • Support submission activities for Canada and United States markets.

🎓 Eligibility Criteria

Candidates with experience in the following international markets will have an advantage:

  • Canada
  • United States
  • Europe
  • Australia
  • New Zealand
  • United Kingdom

Strong knowledge of regulatory documentation, dossier compilation, eCTD systems, and submission management will be preferred.

📑 Documents Required for Interview

Applicants should carry the following documents during the walk-in drive:

✅ Updated Resume/CV

✅ Recent Passport Size Photographs

✅ Current Employer Appointment Letter

✅ Last Three Months Salary Slips

✅ Educational Certificates and Experience Documents (if applicable)

⚠️ Important Notice

Candidates who have attended an interview with JAMP India Pharmaceuticals within the last 30 days will not be considered for this recruitment drive.

🛡️ Recruitment Fraud Warning

JAMP India Pharmaceuticals follows a direct recruitment process and does not authorize external consultants or agents to collect money from candidates.

Applicants are advised not to pay any fee for interviews, job offers, or recruitment-related activities.

📧 Unable to Attend the Walk-In?

Candidates who cannot attend the interview in person may submit their resumes through email.

Email: hrindia@jamppharma.com

Suggested Subject Line:
Application for Regulatory Affairs – [Position Name] – [Years of Experience]

Online Application Form

Apply Here:
https://docs.google.com/forms/d/e/1FAIpQLSfDs6Mr1crO-hX5gm6lDywn4Ih7VxhMyq_Upp6QBwo73iH2tw/viewform

🌟 Why Join JAMP India Pharmaceuticals?

  • Exposure to highly regulated global pharmaceutical markets
  • Opportunities to work on international submissions
  • Career growth in Regulatory Affairs and eCTD operations
  • Collaborative and professional work environment
  • Learning opportunities for fresh graduates and experienced professionals

Professionals seeking long-term growth in pharmaceutical regulatory affairs should not miss this excellent opportunity to join a growing global organization.

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