JAMP India Pharmaceuticals Hiring Regulatory Affairs Executive (Post-Commercials) – B Pharm/M Pharm, Ahmedabad
- JAMP India Pharmaceuticals Hiring Regulatory Affairs Executive
- About JAMP India Pharmaceuticals Pvt. Ltd.
- Position Title: Regulatory Affairs Executive (Post-Commercials)
- Job Location
- Preferred Language
- Qualification
- Experience
- Job Description
- Role: Regulatory Affairs Executive (Post-Commercials)
- How to Apply
JAMP India Pharmaceuticals Hiring Regulatory Affairs Executive
JAMP India Pharmaceuticals Pvt. Ltd. is seeking a skilled and experienced Regulatory Affairs Executive (Post-Commercials) to join our team in Ahmedabad. We are looking for candidates with a B.Pharm or M.Pharm degree and 2-4 years of relevant experience in the pharmaceutical industry. This is a fantastic opportunity to contribute to high-quality regulatory submissions and collaborate with a dynamic team. Apply now to be part of a leading pharmaceutical company.
About JAMP India Pharmaceuticals Pvt. Ltd.
JAMP India Pharmaceuticals Pvt. Ltd. is a renowned name in the pharmaceutical industry, dedicated to providing high-quality healthcare solutions. Our Regulatory Affairs (Post-Commercials) team is instrumental in ensuring compliance and smooth market operations for our products. With a focus on excellence and innovation, we strive to bring the best pharmaceutical products to the market.
Position Title: Regulatory Affairs Executive (Post-Commercials)
Job Location
- Ahmedabad
Preferred Language
- English
- Hindi
- Regional languages
Qualification
- B.Pharm
- M.Pharm
Experience
- 2-4 years of relevant experience in the Pharmaceutical Industry
Job Description
Role: Regulatory Affairs Executive (Post-Commercials)
As a Regulatory Affairs Executive at JAMP India Pharmaceuticals, your key responsibilities will include:
- Preparing, coordinating, and compiling quality regulatory submissions (Level I, Level III, and Level IV) to Health Canada for marketed products.
- Preparing and reviewing responses to Health Canada requests and deficiency letters in a timely manner to ensure prompt regulatory approvals under the supervision of the Deputy Manager.
- Liaising with internal and external stakeholders to assemble necessary documentation for post-approval submissions.
- Providing regulatory support for projects related to the transfer of product manufacturing sites.
- Collaborating with the product launch team for strategic product launches.
How to Apply
Interested candidates who meet the qualification criteria can send their CV to praval@jamppharma.com
