MSc Life Science Jobs at Teva Pharmaceuticals | Apply Now for Regulatory Affairs Associate Position
Are you looking for an exciting career opportunity in the pharmaceutical industry? Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I in Navi Mumbai, India. This role offers the chance to work with a global leader in generic medicines, contributing to regulatory support for European and International Markets while developing expertise in compliance, documentation, and cross-functional collaboration.
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making good health more affordable and accessible. With operations in nearly 60 countries, Teva’s medicin
es improve the lives of millions of patients every day. As the world’s largest producer of generic medicines, Teva is proud to have many of its products included on the World Health Organization’s Essential Medicines List. Every day, around 200 million people rely on Teva medicines. Our diverse workforce, innovative research, and dedication to high-quality healthcare solutions make Teva an employer of choice for professionals seeking to make a real impact worldwide.Job Details
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, India, 400706
- Company: Teva Pharmaceuticals
- Job ID: 64000
Qualification:
- Master’s in Pharmacy or Master’s in Science/Life Sciences.
- College or University degree, or equivalent work experience, providing knowledge of regulatory principles.
Experience:
- 2–3 years of pharmaceutical industry experience, ideally in Regulatory Affairs (RA). R&D, Development, or QA experience may also be considered.
- Experience with regulatory documentation for Europe and/or International Markets.
Knowledge & Skills:
- Understanding of regulatory concepts and procedures.
- Ability to apply internal procedures to standard problems.
- Proficiency in regulatory IT systems for compliance and documentation.
- Working knowledge of Office 365 and Veeva Vault.
- Strong compliance and regulatory focus.
- Basic project management knowledge.
- Strong organizational skills to meet personal, team, and company goals.
- Ability to escalate decisions or issues beyond personal competence.
- French and/or German language skills are an advantage.
How You’ll Spend Your Day
- Complete designated projects and tasks supporting European and International Market RA according to internal Work Instructions, under guidance from managers and senior colleagues.
- Maintain documentation and regulatory IT systems in line with internal procedures.
- Ensure timely completion of tasks with accurate tracker updates and adherence to compliance standards.
- Communicate with Teva units across Europe, International Markets, third parties, and Health Authorities.
- Fulfill departmental duties and ad-hoc tasks as assigned by senior RA staff.
- Complete mandatory training through Teva’s learning management system within defined timeframes.
- Attend team meetings and provide updates on assigned activities and tasks.
- Stay informed on current and pending regulatory legislation and guidelines.
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