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:

• 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

Application Link