Teva Pharmaceuticals is a global leader in generic and specialty medicines, dedicated to improving patient health by providing high-quality, affordable healthcare solutions. As the world’s largest generic drug manufacturer, Teva operates in over 60 countries, ensuring access to life-saving medications worldwide.
📍 Location: Navi Mumbai, India
📅 Last Date to Apply: 31st August 2025
🔍 Job ID: 63515
Job Description: Regulatory Affairs Associate III
Key Responsibilities:
✔ Prepare, compile, and submit high-quality regulatory submissions for post-approval activities in compliance with Health Canada (HC) regulations.
✔ Develop and implement regulatory strategies for assigned projects to ensure timely approvals.
✔ Collaborate with R&D and cross-functional teams to align regulatory requirements with business goals.
✔ Evaluate change controls and assess regulatory filing impacts as per HC guidelines.
✔ Stay updated with Health Canada, ICH, and Teva’s internal regulatory guidelines.
✔ Support business development assessments related to regulatory compliance.
Candidate Profile:
✅ Education: M.Pharma in a scientific discipline.
✅ Experience:
- 5-7 years in Regulatory Affairs (Post-Approval – EU/FDA, HC preferred)
- 7-10 years overall pharmaceutical industry experience
- Experience with sterile products is a plus
✅ Skills Required: - Strong regulatory writing & communication skills
- Excellent organizational & multitasking abilities
- Critical thinking & attention to detail
Why Join Teva Pharmaceuticals?
- 🌍 Global exposure in the pharmaceutical industry
- 💼 Career growth in regulatory affairs & compliance
- 🏆 Work with a leader in generic medicines
- 📈 Innovative & collaborative work environment
How to Apply?
If you meet the eligibility criteria, apply before 31st August 2025.
