Life Science Jobs at Teva Pharmaceuticals
Explore an exciting opportunity as a Regulatory Affairs Role at Teva Pharmaceuticals in Navi Mumbai. Contribute to global regulatory data management, ensure compliance with xEVMPD and Article 57 requirements, and help shape the future of healthcare with one of the world’s leading pharmaceutical companies with the Life Science Jobs.
Job Details:
- Job ID: 64411
- Date Posted: October 16, 2025
- Location: Navi Mumbai, India, 400706
- Department: Global Regulatory Affairs
- Employment Type: Full-time
- Experience Required: 2-5 years in regulatory operations/affairs
- Educational Requirements: Bachelor’s or Master’s in Life Sciences or IT (MS preferred)
Regulatory Affairs Role Description:
The role of GRO Regulatory Data Analytics is to manage Teva’s data in accordance with requirements for xEVMPD in order to maintain Teva’s Article 57 compliance. This position also involves providing a Central Data Service for the creation and maintenance of GRA product registration data in line with the global needs of Teva Global Regulatory Affairs, and offering SME services for data management processes and execution in current and future regulatory data systems.
About Teva Pharmaceuticals:
Teva Pharmaceuticals is a leading global manufacturer of generic medicines and a producer of many products on the WHO Essential Medicines List. Operating in nearly 60 countries, Teva helps over 200 million people take their medicines daily while driving innovation to make healthcare more affordable and accessible.
Qualifications and Experience:
- Minimum Educational Qualifications: Bachelor’s or Master’s Degree in Life Sciences or Information Technology
- Minimum Years of Work Experience: 2-5 years (Preferred experience in regulatory operations/affairs)
Key Responsibilities:
- At Teva Pharmaceuticals, you have to execute GRO Regulatory Data Analytics operations in line with SOPs and Work Instructions
- Manage product registration data and understand regulatory dossier structures
- Perform Quality Control (QC) and ensure data integrity in the Teva Global Registration database
- Represent Regulatory Data Analytics within the wider Global Regulatory Affairs community
- Support projects improving regulatory data quality, system integration, and regulatory technology changes
- Assist the Manager with data management process execution and oversight
- Coach and develop team members aligned with organizational needs
- Operate Regulatory Data Analytics processes including RIM data administration
- Identify opportunities for process improvement and implement change
- Support industry and company initiatives impacting regulatory data management practices
Skills Required:
- For the Regulatory Affairs Role, you need strong knowledge of regulatory data management and registration workflows
- Proficiency in navigating and understanding regulatory dossiers
- Analytical skills for data QC and integrity checks
- Excellent stakeholder communication and collaboration skills
- Ability to implement process improvements in a professional regulatory environment
- Project management and system integration support experience
How to Apply?
Candidates can apply through the Teva Pharmaceuticals careers portal or subscribe to job alerts on the official website to receive updates on similar opportunities.
