About Company:
JAMP India Pharmaceuticals Pvt. Ltd is a company part of JAMP Pharma Group, a Canadian privately-owned pharmaceutical organization founded 35 years ago. We are focused exclusively on providing high quality medicines and healthcare solutions for patients and consumers. At JAMP India Pharmaceuticals Pvt. Ltd, 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. Encouraging internal promotion of our employees and the growth of our workforce, JAMP India Pharmaceuticals Pvt. Ltd is constantly on the lookout for talented candidates who want to thrive in a stimulating work environment. Be part of a company that values passion and the desire to make a difference! As part of JAMP India Pharmaceuticals Pvt. Ltd, 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 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.
Vacancy Details:
Job Description:
WE ARE HIRING!
Join our Regulatory Affairs Biosimilar Team!
JAMP India Pharmaceuticals is growing, and we’re currently looking for talented professionals to join our team in Ahmedabad.
Department: Regulatory Affairs – Biosimilars
Position: Officer/Senior Officer
Experience: 1-3 years
Qualification: B. Pharma/M. Pharma
Location: Ahmedabad
Key Responsibilities:
1.Assist in the preparation of assigned post-approval submissions (e.g., Notifiable Changes, Supplemental New Drug Submission) and New Drug Submissions, under supervision.
2.Assist in the preparation of response packages to Health Canada requests in a timely manner to minimize delays in the submission review process.
3.With supervision, ensure documentation prepared in scope of assigned projects/tasks is accurately presented, scientifically sound, and encompasses all relevant material necessary for a complete submission by referring to appropriate guidance.
You would be assisting in the preparation of post-approval submissions and New Drug Submissions. Also, supporting the timely submission of response packages to Health Canada and documentation.
How to Apply?
Interested candidates can send their profiles to dkothari@jamppharma.com.
