Jamp Pharma Walk In Interview For Regulatory Affairs Professionals 


1) Department: Regulatory Affairs – CMC Canada

Designation: Assistant Manager

Openings: 2 positions

Qualification: M. Pharm / B. Pharm

Experience Required: 6 to 8 years of relevant experience

Market Focus: Canada / US / EU

Role Overview Responsible for finalizing new drug submissions including drafting and reviewing the Quality Overall Summary. Responding to regulatory letters and managing post-approval activities. The role involves leadership of team members, managing daily functions, and collaborating with internal teams and external partners to drive project success.


2) Department: Regulatory Affairs – CMC Australia

Designation: Assistant Manager

Openings: 1 position

Qualification: M. Pharm / B. Pharm

Experience Required: 6 to 8 years of relevant experience

Market Focus: Australia (with exposure to Canada / EU Market)

Role Overview Manage the preparation and finalization of drug submissions, oversee responses to regulatory agencies, and support post-approval documentation. The role demands leadership, mentoring, and proactive engagement with cross-functional teams and third-party collaborators.


3) Department: Regulatory Affairs – CMC Canada

Designation: Senior Executive (4), Executive (2), Senior Officer (2)

Openings: 8 positions

Qualification: M. Pharm / B. Pharm

Experience Required: 3 to 6 years of relevant experience 

Market Focus: Canada / US / EU

Role Overview Responsible for compilation, review, and timely submission of ANDS and Health Canada deficiency responses. Extend documentation alignment with HC guidelines during product development. Support regulatory functions and promote Good Manufacturing Practices (GMP).


4) Department: Regulatory Affairs – eCTD DMS

Designation: Senior Officer / Executive

Openings: 2 positions

Qualification: M. Pharm / B. Pharm

Experience Required: 2 to 5 years of relevant experience

Role Overview Implementation and maintenance of the Document Management System with support during late-night operations. Responsible for eCTD compilation, validation, and submissions to Health Canada, US (via ESG Gateway), and export markets, including lifecycle management and tracking of daily submissions.


Interview Details Walk-In Interview

Date: Saturday, July 5

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

Additional Notes Interested candidates should bring an updated resume, passport-size photograph, last three months' salary slips, and an appointment letter.

Those unable to attend can apply by scanning the QR code or emailing their resume to hrindia@jamppharma.com.

Candidates interviewed within the last month are requested not to apply. JAMP India does not engage consultants/agents promising interviews for a fee.

Jamp Pharma Walk In Interview For Regulatory Affairs Professionals

Jamp Pharma Walk In Interview For Regulatory Affairs Professionals 

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