About Company:
JAMP Pharma, including its affiliates, is a privately owned Canadian company whose head office is located in Boucherville, 20 minutes from Montreal. Having experienced phenomenal growth, we are among the leading players in the generic pharmaceutical industry in Canada, with close to 345 molecules in our portfolio. JAMP Pharma also owns the natural health products Wampole, Laboratoire Suisse, Cosmétique Import and prescription products from Orimed Pharma. With the primary goal of providing quality health products, the departments of sales, research and development, logistics, customer service, quality assurance, regulatory affairs, market access, marketing, business development and export are committed to provide excellent customer service on a daily basis. Our employees stand out for their willingness to go the extra mile for our customers. We foster a work environment where innovation, teamwork and recognition are present. Our values are based on performance, passion, open communication, respect, integrity and customer satisfaction. With a turnover that has been growing steadily for more than 10 years, encouraging the promotion of our employees internally and the growth of our workforce, JAMP Pharma is regularly looking for talented candidates who want to thrive in a stimulating work environment. As part of JAMP Pharma, you will be able to: • Achieve your professional goals while having a significant impact on the success of the company. • Perform in a fast, agile, entrepreneurial and friendly environment. • Work with talented and multicultural professionals in order to achieve common goals. • Be part of a stable, successful and ambitious company at the forefront of innovation • Take advantage of our new, bright and welcoming offices. • Get involved socially with employees as well as the community. WANT TO MAKE HISTORY WITH US?
Vacancy Details:
Job description:
Walk-In Interview on 5th July (Saturday) for our Regulatory Affairs Team!
JAMP India Pharmaceuticals Pvt. Ltd. is seeking passionate and driven professionals to join our Regulatory Affairs Team. This is a valuable opportunity for professionals looking to grow within a dynamic and expanding organization committed to excellence.
We are looking for candidates with proven expertise in: Regulatory Submissions, Dossier Preparation and Query handling for regulated markets – Canada, Australia, US and Europe.
Walk-In Interview For Regulatory Affairs – Canada & Australia Market
1.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
1.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.
2. Provide leadership, mentoring to the Team Leads and Associates and manage day-to- day functioning of the assigned roles.
3.Working closely with cross functional teams within the organization and third party teams and maintain good collaboration with all parties for the ongoing projects.
2.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
1.Compile, review and timely submission of ANDS and Deficiencies responses received from Health Canada
2.Support Cross-functional as 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.
3.Promotes Good Manufacturing Practices (GMP).
3.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)
1.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.
2.Provide leadership, mentoring to the Team Leads and Associates and manage day-to- day functioning of the assigned roles.
3.Working closely with cross functional teams within the organization and third party teams and maintain good collaboration with all parties for the ongoing projects.
4.REGULATORY AFFAIRS – ECTD DMS (2 POSITIONS)
Designation: Senior Officer / Executive
Qualification: M. Pharm / B. Pharm
Experience: 2-5 years of relevant experience
1.Implementing & Maintaining Document Management System and late night support
2.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.).
3.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.
How to Apply?
Date & time: Saturday, July 5 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
Candidates who are not able to attend the Walk-In can send their updated resume to hrindia@jamppharma.com or scan the QR code as mentioned and apply.
Scan & apply online (for candidates not able to attend the Walk-In)
Candidates who are unable to attend the walk-in interview can send their profile to hrindia@jamppharma.com
