Interview for Regulatory Affairs at JAMP Pharma - Canada & Australia Market

The JAMP group is a proud Canadian owned company with its international headquarters located in Boucherville, 20 minutes from downtown Montreal, Quebec, Canada. The JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma Generics, Orimed branded products, our Wampole and Laboratoire Suisse natural health supplements and our Cosmetic Import beauty and personal care products.

Walk-In Interview for Regulatory Affairs - Canada & Australia Market

Regulatory Affairs - CMC Canada (2 Positions)
Designation : Assistant Manager
Qualification : M.Pharm / B.Pharm
Experience : 6 - 8 years of relevant experience
Market : Canada/ US/ EU Market
Finalize the preparation of new drug submissions (Drafting and reviewing the Quality Overall Summary), deficiencies to regulatory letters and post approval activities for the given portfolio of products.
Provide leadership, mentoring to the Team Leads and Associates and manage day-to- day functioning of the assigned roles.
Working closely with cross functional teams within the organization and third party teams and maintain good collaboration with all parties for the ongoing projects.

Regulatory Affairs - CMC Australia (1 Position)
Designation : Assistant Manager
Qualification : M.Pharm / B.Pharm
Experience : 6 - 8 years of relevant experience
Market : Australia Market (Along with exposure to Canada/ EU Market)
• Finalize the preparation of new drug submissions (Drafting and reviewing the Quality Overall Summary), deficiencies to regulatory letters and post approval activities for the given portfolio of products.
• Provide leadership, mentoring to the Team Leads and Associates and manage day-to- day functioning of the assigned roles.
• Working closely with cross functional teams within the organization and third party teams and maintain good collaboration with all parties for the ongoing projects.

Regulatory Affairs - Cmc Canada (8 Positions)
Designation : Senior Executive (4) / Executive (2) / Senior Officer (2)
Qualification : M.Pharm / B.Pharm
Experience : 3 - 6 years of relevant experience
Market : Canada/ US/ EU Market
• Compile, review and timely submission of ANDS and Deficiencies responses as received from Health Canada
• Support Cross-functional team like Analytical Development, Formulation Development during product development and align documentation as per HC guidelines and Extend support for any other Regulatory related Function.
• Promotes Good Manufacturing Practices (GMP).

Regulatory Affairs - ECTD Dms (2 Positions)
Designation : Senior Officer / Executive
Qualification : M.Pharm / B.Pharm
Experience : 2 - 5 years of relevant experience
• Implementing & Maintaining Document Management System and late night support eCTD Compilation, validation, and submission to Health Canada and US through ESG gateway for :
* New Submission (ANDS/NDS)
* Deficiencies response (Clarifax, SDN, NOD, NON etc.)
* Supplements submissions (sANDS, ARs, Safety updates, RMPs etc.).
• eCTD compilation, validation, and submission to export market, lifecycle management of products and maintaining daily submission tracking.

• Interested candidates can Walk-In for interview along-with their updated resume, passport size photograph, Last three months Salary Slips and appointment letter.
• Candidates who have been interviewed in the past one month are requested not to reapply.
• Please note that JAMP India Pharmaceuticals Pvt. Ltd. does not hire through consultants / agents who promise interviews / jobs for monetary consideration / registration fees. Beware of such fraudulent calls.
• Candidates who are not able to attend the Walk-In can send their updated resume to hrindia@jamppharma.com or apply online.

Walk in Interview
Saturday, July 5 10:00 AM to 4:00 PM
JAMP India Pharmaceuticals Pvt. Ltd.
A-1207,12th Floor, Navratna Corporate Park, Ambli Bopal road, Ambli, Ahmedabad - 380058