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Teva Pharmaceuticals — a global leader in generic medicines and healthcare innovation — is inviting applications for the role of Regulatory Affairs Associate I in Navi Mumbai, India.
This position is ideal for B.Pharm, M.Pharm, or Life Science postgraduates passionate about regulatory publishing, eCTD submissions, and compliance. You’ll play a key role in ensuring high-quality regulatory submissions for major markets like the EU, US, and Canada, helping millions worldwide access affordable healthcare.
📋 Key Responsibilities
As a Regulatory Affairs Associate I, you’ll:
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- Publish and dispatch major and complex eCTD submissions for EU, US, and Canada markets.
- Handle post-approval submissions, ensuring timely and high-quality dispatch to regulatory agencies.
- Perform document-level publishing, troubleshooting issues, and executing quality control checks.
- Collaborate with cross-functional scientific and regulatory teams for submission planning and execution.
- Maintain a strong working knowledge of ICH and eCTD guidelines.
- Work with regulatory tools and systems like Veeva Vault, Global Insight, ISI Toolbox, Lorenz Validator, and Adobe Acrobat.
🎓 Qualifications and Experience
- Educational Qualification: B.Pharm / M.Pharm / M.Sc. in Life Sciences
- Experience: 1–3 years (preferably in Regulatory Publishing for EU and US markets)
- Strong communication skills (written and verbal)
- Familiarity with regulatory IT systems
- Ability to work effectively in global, multicultural environments
💼 Why Join Teva Pharmaceuticals?
At Teva, you’ll be part of a diverse and inclusive global community working to make good health more affordable and accessible. Teva offers:
- Competitive salary and benefits
- Exposure to international regulatory markets
- Growth opportunities in a world-class pharmaceutical environment
- Work-life balance and continuous learning support
📝 How to Apply
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