Teva Pharmaceuticals, a global leader in generic medicines, is hiring a Regulatory Affairs Associate I for its Navi Mumbai office. This is a great opportunity for candidates with 1–3 years of experience in regulatory affairs or regulatory data management to build a career in the pharmaceutical industry.
Working at Teva means contributing to making healthcare more affordable and accessible, with products that impact over 200 million patients worldwide every day.
Key Responsibilities
As a Regulatory Affairs Associate I, you will:
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- Execute regulatory data analytics operations in line with SOPs and work instructions.
- Manage product registration data by extracting information from regulatory dossiers.
- Perform Quality Control (QC) and data integrity checks to ensure accuracy of Teva’s Global Registration Database.
- Represent Regulatory Data Analytics across Global Regulatory Affairs teams and build strong stakeholder relationships.
- Contribute to projects improving regulatory data quality, system integration, and technology upgrades.
Qualifications & Skills
Education:
- Bachelor’s or Master’s degree in Life Sciences or Information Technology (required).
- MS in scientific or IT discipline (preferred).
Experience:
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- 1–3 years in regulatory operations/affairs or regulatory data management.
Required Skills:
- Interest in pharmaceutical regulatory affairs.
- Strong aptitude for regulatory data handling.
Preferred Skills:
- Prior experience in regulatory product registration data management.
- Familiarity with Regulatory Information Management (RIM) systems.
Benefits of Joining Teva
- Work with a global leader in generics and biosimilars.
- Exposure to regulatory data systems and advanced compliance operations.
- Opportunity to grow in regulatory affairs with mentorship from industry experts.
- Inclusive and diverse workplace culture.
How to Apply
