JAMP India Pharmaceuticals is a leading pharmaceutical company committed to innovation and excellence in drug development and regulatory compliance. With a focus on biosimilars and cutting-edge pharmaceutical products, JAMP strives to deliver high-quality medicines that improve patient outcomes. The company fosters a collaborative work environment and offers opportunities for professional growth in the regulatory affairs domain.
Job Description: Regulatory Affairs Officer/Senior Officer – Biosimilars
Key Responsibilities:
- Assist in the preparation of post-approval submissions such as Notifiable Changes and Supplemental New Drug Submissions.
- Support the preparation of New Drug Submissions under supervision.
- Prepare timely response packages to Health Canada requests to minimize delays in submission reviews.
- Ensure all documentation for assigned projects is scientifically sound, accurate, and complete by referring to relevant regulatory guidelines.
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
Specifications:
- Department: Regulatory Affairs
- Experience: 1-3 Years
- Qualification: B. Pharma / M. Pharma
- Location: Ahmedabad, India
Why Work at JAMP India Pharmaceuticals?
- Opportunity to work with a reputed pharmaceutical company specializing in biosimilars.
- Gain hands-on experience in regulatory submissions and compliance.
- Work in a dynamic and supportive environment.
- Enhance your career growth in the pharmaceutical regulatory affairs sector.
How to Apply
Interested candidates can send their updated resume to dkothari@jamppharma.com. Alternatively, scan the QR code provided in the job posting to apply directly.
