JAMP India Pharmaceuticals Regulatory Affairs Jobs for CMC and eCTD Professionals
JAMP India Pharmaceuticals Pvt. Ltd. is conducting a walk-in interview for Regulatory Affairs professionals at its Ahmedabad office. The company is hiring experienced candidates for CMC Canada and eCTD departments with exposure to Canada, Australia, New Zealand, UK and Europe markets. This is an excellent opportunity for Regulatory Affairs professionals looking to grow in an international pharmaceutical environment.
JAMP India Pharmaceuticals Hiring for Below Positions
1) Department: Regulatory Affairs – CMC Canada
Designation: Manager / Deputy Manager / Assistant Manager
Experience: 7 to 12 Years of relevant experience
Qualification: M.Pharm / B.Pharm
Key skill or job description:
- Market: Canada/US/EU/Australia/New Zealand Market is Mandatory.
- Review and finalize preparation of new drug submissions, deficiencies to regulatory letters and post approval activities.
- Provide leadership to the team leads and associates.
- Work closely with cross functional teams.
- Any other duties assigned.
2) Department: Regulatory Affairs – CMC Canada
Designation: Senior Executive / Executive
Experience: 7 to 9 Years of relevant experience
Qualification: M.Pharm / B.Pharm
Key skill or job description:
- Market: Canada/US/EU/Australia/New Zealand Market is Mandatory.
- Compile, review and timely submission of ANDS.
- Review deficiency responses received from Health Canada/Australia.
- Support cross-functional teams.
- Promote Good Manufacturing Practices (GMP).
- Any other duties assigned.
3) Department: Regulatory Affairs – CMC Canada
Designation: Trainee Officer
Experience: 7 to 9 Years of relevant experience
Qualification: M.Pharm / B.Pharm
Key skill or job description:
- Preference: Specialization in RA or Pharmaceuticals.
- Candidates with internship in RA department are preferred.
- Compile, review and timely submission of ANDS.
- Support cross-functional teams.
- Promote Good Manufacturing Practices (GMP).
- Any other duties assigned.
4) Department: Regulatory Affairs – eCTD
Designation: Senior Officer / Officer / Trainee Officer
Experience: 0 to 3 Years of relevant experience
Qualification: M.Pharm / B.Pharm
Key skill or job description:
- Canada/US/EU/Australia/New Zealand Market is Mandatory.
- Freshers can appear.
- eCTD compilation, validation and submission.
- New submissions (ANDS/NDS).
- Deficiency responses.
- Supplements submissions.
- Maintaining daily submission tracking.
- Any other duties assigned.
Walk-In Interview Details
Work Location: Ahmedabad, Gujarat
Interview Date: Sunday, 05 July
Time: 10:00 AM to 4:00 PM
Venue: A-1207, 12th Floor, Navratna Corporate Park, Ambli Bopal Road, Ambli, Ahmedabad – 380058
Candidates unable to attend can send their updated resume to hrindia@jamppharma.com or scan the QR code mentioned in the advertisement.
Who Can Apply
- Candidates with M.Pharm or B.Pharm qualification.
- Professionals having relevant Regulatory Affairs experience in CMC Canada or eCTD.
- Freshers can apply only for the eCTD Trainee Officer role as mentioned in the advertisement.
Career Growth at JAMP India Pharmaceuticals
JAMP India Pharmaceuticals offers excellent opportunities to work on global regulatory submissions for Canada, Australia, New Zealand, UK and European markets. Employees gain exposure to international regulatory requirements, ANDS submissions, eCTD lifecycle management, GMP practices and cross-functional pharmaceutical development projects.
Frequently Asked Questions
1. Which departments are hiring?
Regulatory Affairs – CMC Canada and Regulatory Affairs – eCTD.
2. What qualification is required?
M.Pharm or B.Pharm.
3. Can freshers apply?
Yes. Freshers can apply for the eCTD Trainee Officer position.
4. What documents should be carried for the interview?
Updated resume, passport-size photograph, last three months’ salary slips and appointment letter.
5. How can candidates apply if they cannot attend the interview?
They can send their updated resume to hrindia@jamppharma.com.
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JAMP India Pharmaceuticals Walk-In Interview for Regulatory Affairs Professionals
