Teva Pharmaceuticals, the world’s leading manufacturer of generic medicines, is hiring Regulatory Affairs Associate I in Navi Mumbai, India. This is an exciting opportunity for B.Pharm or M.Pharm graduates with 1–4 years of Regulatory Affairs (RA) experience in EU and international markets.
At Teva, you’ll join a global team impacting millions of lives every day by making essential medicines accessible and affordable.
🔹 Key Responsibilities
As a Regulatory Affairs Associate I, you will:
- Manage lifecycle activities for specific products in EU and international markets.
- Ensure all regulatory modules under your responsibility are updated as per procedures.
- Prepare and submit variations to authorities or Teva’s 3rd party client business (Medis).
- Track submissions, approvals, and timelines.
- Compile and respond to deficiency questions from authorities and clients.
- Communicate outcomes of variations promptly and update regulatory databases.
- Provide regular status updates to management.
- Collaborate with internal and external stakeholders on RA projects.
🎓 Qualifications & Experience
- Education: B.Pharm or M.Pharm.
- Experience: 1–4 years in Regulatory Affairs, specifically with EU and International markets.
- Skills & Traits:
- Strong organizational and communication skills.
- Excellent written and verbal English.
- Strategic thinker with flexibility.
- Team player with proactive work style.
- Proficient computer skills.
🌟 Why Join Teva Pharmaceuticals?
- Work with a global leader in generics and specialty medicines.
- Be part of a mission-driven company improving access to healthcare worldwide.
- Gain exposure to EU & international regulatory frameworks.
- Collaborative and inclusive work environment.
- Career growth opportunities in Regulatory Affairs.
📌 How to Apply
