Teva Pharmaceuticals, one of the world’s leading manufacturers of generic medicines, is inviting applications for three Regulatory Affairs positions across Navi Mumbai and Bangalore. These openings offer an excellent opportunity for professionals with experience in Regulatory Publishing, US FDA submissions, eCTD, and post-approval lifecycle management to build a long-term career in a global pharmaceutical organization.
With products used daily by over 200 million patients worldwide, Teva continues to strengthen its Regulatory Affairs teams to support high-quality, compliant submissions for the US, EU, and Canadian markets.
Open Positions at Teva Pharmaceuticals
1. Regulatory Affairs Associate I – RA Publishing
📍 Location: Navi Mumbai, Maharashtra
🆔 Job ID: 64525
🗓 Experience: 1–3 years
Key Responsibilities
- Publish and dispatch eCTD submissions for US, EU, and Canada
- Handle post-approval lifecycle submissions
- Perform document-level publishing, QC checks, and troubleshooting
- Collaborate with Regulatory and Scientific teams
- Ensure compliance with ICH, eCTD, NeeS, and agency guidelines
- Work on systems like Veeva Vault, Global Insight, Lorenz Validator, ISI Toolbox
Qualifications
- B.Pharm / M.Pharm / Master’s in Life Sciences
- Experience in Regulatory Publishing (US/EU preferred)
- Strong command of written and spoken English
- Familiarity with regulatory IT systems
2. Associate II – Complex Generics, Regulatory Affairs
📍 Location: Bangalore, Karnataka
🆔 Job ID: 63167
🗓 Experience: 4+ years
Key Responsibilities
- Prepare and submit US FDA filings for complex generics
- Handle ANDA submissions, amendments, deficiency responses
- Manage post-approval changes (PAS, CBE-30, CBE-0, Annual Reports)
- Support FDA engagement strategies for first-cycle approvals
- Act as regulatory point of contact for cross-functional teams
- Track FDA guidance, Orange Book, and Drugs@FDA updates
Qualifications
- Master’s degree in Regulatory Affairs / Quality Assurance
- Experience with inhalation, ophthalmic, implant, or drug-device products
- Strong knowledge of FDA and ICH guidelines
- Excellent analytical, organizational, and communication skills
3. Regulatory Affairs Associate II
📍 Location: Navi Mumbai, Maharashtra
🆔 Job ID: 64918
🗓 Experience: 4+ years
Key Responsibilities
- Maintain approved ANDAs and Annual Reports
- Independently compile and publish post-approval submissions
- Evaluate and classify change controls
- Maintain regulatory trackers and databases
- Train Associate I team members on internal systems and SOPs
Qualifications
- M.Pharm (RA/QA preferred)
- Experience in US FDA post-approval regulatory activities
- Strong documentation, coordination, and multitasking abilities
Why Join Teva Pharmaceuticals?
- Global exposure to US FDA and EU regulatory submissions
- Inclusive and diverse work culture
- Opportunity to work on essential medicines
- Strong focus on quality, compliance, and professional development
- Competitive compensation and long-term career growth
Estimated Salary Range (India)
- Associate I: ₹6 – ₹9 LPA
- Associate II: ₹10 – ₹18 LPA
(Salary may vary based on experience and role complexity)
How to Apply
Application Link For Regulatory Affairs Associate I – RA Publishing
Application Link For Associate II – Complex Generics, Regulatory Affairs
Application Link For Regulatory Affairs Associate II
