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Teva Pharmaceuticals, a global leader in generic medicines, is inviting applications for the position of Regulatory Affairs Associate I at its Navi Mumbai location. This role is part of Teva’s Global Regulatory Operations (GRO) – Regulatory Data Analytics team and plays a critical role in ensuring Article 57 and xEVPMD compliance across global markets.
This opportunity is ideal for early-career regulatory affairs professionals with a strong interest in regulatory data management, product registration data, and regulatory information management systems (RIMS).
Key Responsibilities
As a Regulatory Affairs Associate I at Teva, you will:
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- Execute Regulatory Data Analytics operations in compliance with SOPs and work instructions
- Manage and maintain global product registration data to support xEVPMD and Article 57 compliance
- Procure and extract regulatory data from source dossiers (CTD/eCTD)
- Perform quality control (QC) and data integrity checks on regulatory databases
- Navigate and interpret regulatory dossiers with accuracy and consistency
- Support global regulatory teams by acting as an SME for regulatory data systems
- Participate in regulatory data quality improvement and system integration projects
- Collaborate cross-functionally within Global Regulatory Affairs
Educational Qualifications
Required:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or Information Technology
Preferred:
- MS or equivalent qualification in a scientific or IT discipline
Experience Requirements
- 1–3 years of experience (preferred exposure to regulatory affairs or regulatory operations)
- Hands-on experience with regulatory data, product registrations, or RIMS is an advantage
Key Skills & Competencies
- Strong interest in pharmaceutical regulatory affairs
- Aptitude for regulatory data analytics and data governance
- Understanding of regulatory submission structures and workflows
- High attention to detail, compliance, and data accuracy
- Ability to work effectively with global stakeholders
Why Join Teva Pharmaceuticals?
- Work with the world’s leading generic medicines company
- Exposure to global regulatory systems and compliance frameworks
- Opportunity to build a long-term career in regulatory affairs and data analytics
- Inclusive, diverse, and employee-centric work culture
- Contribution to medicines used by 200+ million patients daily worldwide
Salary & Benefits
- Estimated Salary: ₹6,00,000 – ₹9,00,000 per annum (INR)
- Health insurance and wellness programs
- Professional development and global exposure
- Hybrid and collaborative work environment
How to Apply
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