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.
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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:
- 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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