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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 facility. This is an excellent opportunity for professionals with a background in Regulatory Affairs, R&D, or Quality Assurance to build their career with one of the most respected pharmaceutical companies in the world.
With over 200 million people using Teva’s medicines daily, your contribution will directly support global healthcare accessibility and compliance with regulatory standards.
🔑 Key Responsibilities
As a Regulatory Affairs Associate I at Teva, you will:
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- Support European and International Markets Regulatory Affairs (RA) projects.
- Maintain documentation and regulatory IT systems as per internal procedures.
- Ensure timely and accurate task completion with compliance to work instructions.
- Collaborate with Teva units across Europe, international markets, and health authorities.
- Provide updates to managers and senior RA staff on project progress.
- Stay updated with evolving regulatory legislation and guidelines.
- Complete internal trainings and participate actively in team meetings.
🎓 Qualifications & Experience
To apply, candidates should meet the following requirements:
- Education:
- Master’s in Pharmacy, Science, or Life Sciences.
- Equivalent work experience may be considered.
- Experience:
- 2–3 years in the pharmaceutical industry.
- Regulatory Affairs experience preferred (R&D/QA acceptable).
- Hands-on with regulatory documentation for Europe/International markets.
- Skills & Knowledge:
- Familiarity with regulatory concepts, compliance, and documentation.
- Proficiency in Office-365 and Veeva Vault systems.
- Strong organizational skills and project management awareness.
- French or German language proficiency is an added advantage.
🌟 Why Join Teva Pharmaceuticals?
- Work with the world’s largest manufacturer of generic medicines.
- Be part of a mission to make healthcare affordable and accessible.
- Exposure to global markets and cutting-edge regulatory systems.
- Inclusive and diverse work culture with equal opportunity.
📌 Application Process
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