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 worldโs largest generic drug manufacturer, Teva operates in over 60 countries, ensuring access to life-saving medications worldwide.
๐ย Location:ย Navi Mumbai, India
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ย Last Date to Apply:ย 31st August 2025
๐ย Job ID:ย 63515
Job Description: Regulatory Affairs Associate III
Key Responsibilities:
โ Prepare, compile, and submit high-quality regulatory submissions for post-approval activities in compliance with Health Canada (HC) regulations.
โ Develop and implement regulatory strategies for assigned projects to ensure timely approvals.
โ Collaborate with R&D and cross-functional teams to align regulatory requirements with business goals.
โ Evaluate change controls and assess regulatory filing impacts as per HC guidelines.
โ Stay updated with Health Canada, ICH, and Tevaโs internal regulatory guidelines.
โ Support business development assessments related to regulatory compliance.
Candidate Profile:
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Education: M.Pharma in a scientific discipline.
โ
Experience:
- 5-7 years in Regulatory Affairs (Post-Approval โ EU/FDA, HC preferred)
- 7-10 years overall pharmaceutical industry experience
- Experience with sterile products is a plus
โ ย Skills Required: - Strongย regulatory writing & communication skills
- Excellentย organizational & multitasking abilities
- Critical thinking & attention to detail
Why Join Teva Pharmaceuticals?
- ๐ย Global exposureย in the pharmaceutical industry
- ๐ผย Career growthย in regulatory affairs & compliance
- ๐ย Work with a leader in generic medicines
- ๐ย Innovative & collaborative work environment
How to Apply?
If you meet the eligibility criteria, apply before 31st August 2025.