Looking to build a strong career in Regulatory Affairs Publishing (eCTD submissions)? Teva Pharmaceuticals has announced an exciting opportunity for the position of Regulatory Affairs Associate I in Navi Mumbai.
This role is ideal for candidates with 1–3 years of experience in regulatory publishing, especially those familiar with EU, US, and Canada submissions, eCTD formats, and regulatory IT systems.
With Teva’s strong global presence in generics and innovative medicines, this position offers excellent exposure to international regulatory submissions and lifecycle management.
📌 Job Overview
- Position: Regulatory Affairs Associate I (RA Publishing)
- Company: Teva Pharmaceuticals
- Location: Navi Mumbai, India
- Experience: 1–3 years
- Qualification: B.Pharm / M.Pharm / Life Sciences
- Job Type: Full-time
- Department: Regulatory Submission Management
💼 Key Responsibilities
- Publish and dispatch eCTD submissions for EU, US, and Canada markets
- Handle post-approval lifecycle submissions
- Perform document-level publishing and QC checks
- Troubleshoot technical issues in submission documents
- Collaborate with cross-functional teams for submission planning
- Ensure compliance with ICH guidelines and regulatory standards
- Maintain knowledge of NeeS, paper submissions, and publishing standards
🎯 Required Skills & Tools
- Strong understanding of eCTD structure and regulatory publishing workflows
- Hands-on experience with tools like:
- Veeva Vault
- Global Insight
- ISI Toolbox
- Lorenz Validator
- Adobe Acrobat
- Familiarity with ICH guidelines and submission formats
- Good communication and documentation skills
🎓 Eligibility Criteria
- Education: B.Pharm / M.Pharm / MSc Life Sciences
- Experience: 1–3 years (Regulatory Publishing preferred)
- Exposure to EU/US regulatory submissions is highly desirable
- Strong English communication skills
- Understanding of Regulatory IT systems
💰 Salary (Estimated)
- ₹4.5 LPA – ₹8 LPA (based on experience & industry benchmarks)
🌟 Benefits of Working at Teva
- Global exposure in regulatory affairs and submissions
- Flexible work culture and career growth opportunities
- Access to internal learning platform “Twist”
- Health and wellness benefits
- Inclusive and diverse work environment
📍 Why This Role is Important
This position sits at the core of Regulatory Affairs Publishing, ensuring that pharmaceutical products meet global compliance standards. You will directly contribute to timely drug approvals and lifecycle management, making it a high-impact role in the pharma industry.
📩 How to Apply
