Regulatory Affairs Job at Teva Pharmaceuticals | Apply Now for Regulatory Affairs Associate Role
Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I for its Navi Mumbai office. This is a strong opportunity for life science graduates looking to build a career in a regulatory affairs job within one of the world’s largest generic medicine manufacturers. If you’re seeking a future-focused life sciences job with global exposure, data management responsibilities, and growth in regulatory operations, this Teva Pharmaceuticals career opportunity is worth applying for.
- Job Position: Regulatory Affairs Associate I
- Location: Navi Mumbai, India – 400706
- Job ID: 64645
About The Company
Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines and a trusted producer of several WHO-listed essential drugs. With a presence in nearly 60 countries, Teva delivers affordable, high-quality healthcare solutions to over 200 million people daily. A Teva Pharmaceuticals career means contributing to meaningful global impact while working in a diverse, collaborative environment.
Job Overview
This position supports the GRO Regulatory Data Analytics function, responsible for:
- Managing Teva’s xEVMPD data to ensure full Article 57 compliance.
- Providing central data services for global regulatory product registration.
- Offering SME support for regulatory data management systems.
The role directly contributes to global regulatory operations by ensuring accurate, compliant, and high-quality registration data.
Key Responsibilities
- Execute Regulatory Data Analytics operations following SOPs and Work Instructions.
- Manage regulatory product registration data, including extracting data from regulatory dossiers—requiring a strong understanding of dossier structure and content.
- Perform regulatory data workflows, quality checks, and data integrity reviews to maintain the Teva Global Registration Database.
- Act as a representative of GRO Regulatory Data Analytics within the Global Regulatory Affairs community.
- Build strong working relationships across stakeholder groups.
- Contribute to business projects involving data quality improvements, system integrations, and regulatory technology enhancements.
- Work as an individual contributor with deep hands-on operational involvement.
Experience & Qualifications
- Minimum Educational Requirements
- Required: Bachelor’s or Master’s degree in Life Sciences or Information Technology.
- Preferred: Master’s degree in scientific or IT disciplines.
- Minimum Experience
- Required: 1–3 years (preferably in regulatory operations or regulatory affairs).
Skills & Job Knowledge
- Required
- Strong interest in pharmaceutical regulatory affairs.
- Aptitude for regulatory data management.
- Preferred
- Experience in the pharmaceutical industry with direct involvement in regulatory affairs.
- Understanding of regulatory processes, data workflows, and regulatory information management systems.
- Experience managing product registration data.
If you’re seeking a structured and globally relevant regulatory affairs job, this Teva Pharmaceuticals opening provides a strong platform to grow in regulatory data management and global compliance functions. With exposure to advanced systems and international workflows, this is an excellent life sciences job opportunity to build a long-term Teva Pharmaceuticals career.
