Teva Pharmaceuticals Hiring Regulatory Affairs Specialist II in Bangalore
Looking for Teva Regulatory Affairs Specialist Jobs in Bangalore? This teva regulatory affairs specialist bangalore opening is listed below. Teva Pharmaceuticals is hiring for the Regulatory Affairs Specialist II position in Bangalore, India. Candidates with a BPharm or MPharm qualification and 1 year of experience in regulatory affairs or a related R&D area, with a focus on compliance activities, can explore this opportunity. The role involves regulatory submissions, product lifecycle management, health authority query responses, labeling activities, and regulatory documentation for international markets. This is an opportunity for pharmacy graduates looking to advance their careers in pharmaceutical regulatory affairs.
Job Details
| Job Details | Information |
|---|---|
| Company Name | Teva Pharmaceuticals |
| Job Position | Regulatory Affairs Specialist II |
| Location | Bangalore, India |
| Job ID | 71029 |
| Educational Qualification | B. Pharm / M. Pharm (preferred) |
| Experience Required | 1 year |
| Experience Area | Regulatory affairs or related R&D area focusing on compliance activities |
| Department / Function | Regulatory Affairs |
| Application Deadline | Not specified |
About the Company
Teva Pharmaceuticals is a leading global biopharmaceutical company with a strong presence in generic and innovative medicines. The company focuses on advancing healthcare through research, development, manufacturing, and the delivery of high-quality medicines worldwide. With expertise in therapeutic areas such as neuroscience and immunology, Teva is committed to addressing patients’ evolving healthcare needs. The company promotes innovation, collaboration, and professional growth while working to improve access to medicines and health outcomes globally.
Job Description
Supporting International Markets (IM) for branded, specialty and generic products.
Key Responsibilities
- Manage lifecycle activities including variations, renewals and responses to health authority queries.
- Support regulatory labeling with market regulatory teams.
- Monitor change controls involving sites, suppliers and global RA processes.
- Ensure marketed products comply with local regulations.
- Maintain regulatory systems and documentation (GRIDS, GI Insights, Teva Art, Veeva).
- Complete GxP training.
- Support AI initiatives.
Eligibility Criteria
- B.Pharm or M.Pharm preferred.
- One year of experience in regulatory affairs or a related R&D area focused on compliance.
Required Skills
- Proficiency in MS Office.
How to Apply
Apply online via the Teva careers listing. Apply only through the official notification / employer link given here.
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Apply online via the Teva careers listing.