Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I – RA Publishing in Navi Mumbai, India. This opportunity is ideal for B.Pharm, M.Pharm, or Life Sciences postgraduates with 1–3 years of experience in regulatory publishing, eCTD submissions, and lifecycle management for EU, US, and Canada markets.
If you are looking to build a career in Regulatory Affairs Publishing, especially in global submissions (EU/US), this role offers structured exposure to eCTD, NeeS, post-approval submissions, and regulatory IT systems within a multinational pharmaceutical organization.
About Teva Pharmaceuticals
Teva is a global biopharmaceutical company known for its strong generics portfolio and innovative medicines in areas such as neuroscience and immunology. With operations worldwide, Teva offers structured growth, inclusive work culture, and international exposure in regulatory compliance and submission management.
Job Details
- Position: Regulatory Affairs Associate I – RA Publishing
- Location: Navi Mumbai, India (400706)
- Experience: 1–3 years (Regulatory Publishing preferred – EU/US market)
- Qualification: B.Pharm / M.Pharm / Master of Life Sciences
- Reporting To: Manager – Regulatory Submission Management
- Job ID: 66406
Key Responsibilities
The Regulatory Affairs Associate I will be responsible for publishing and dispatching regulatory submissions with complete quality compliance and timeline adherence.
Core Responsibilities:
- Publish and dispatch major and complex eCTD submission projects for EU, US, and Canada.
- Handle post-approval lifecycle management submissions.
- Perform document-level publishing activities.
- Conduct quality control checks for submission-ready documents.
- Troubleshoot document-related technical issues.
- Collaborate with scientific and regulatory personnel for planning and submission preparation.
- Ensure compliance with ICH guidelines and eCTD/NeeS specifications.
- Work on regulatory IT systems such as:
- Global Insight
- Veeva Vault
- ISI Toolbox
- Adobe Acrobat
- Lorenz Validator
This Regulatory Affairs Publishing job in Mumbai focuses on accuracy, compliance, and timely submission to global health authorities.
Required Qualifications
To apply for this Regulatory Affairs Associate job at Teva, candidates must have:
- B.Pharm / M.Pharm / Master’s in Life Sciences
- 1–3 years of experience in Regulatory Publishing (preferred EU & US submissions)
- Strong understanding of:
- eCTD submission structure
- ICH guidelines
- Regulatory IT systems
- Excellent written and spoken English
- Ability to work in a culturally diverse global environment
- Good understanding of regulatory submission lifecycle management
Benefits & Career Growth at Teva
Teva offers structured career development and employee-centric policies, including:
- Competitive compensation package
- Annual leave and reward plans
- Flexible working schedules (role-dependent)
- Health and wellbeing support programs
- Access to “Twist” career development platform
- Internal mobility and growth opportunities
This Regulatory Affairs Associate I role provides long-term career growth in global regulatory operations.
Salary (Estimated)
Based on market standards for 1–3 years experience in Regulatory Affairs Publishing in Mumbai:
₹4.5 LPA – ₹7.5 LPA (Estimated Range)
Final compensation will depend on experience and internal pay structure.
How to Apply
