Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.
Post : Mgr Regulatory Affairs
Job Description
The opportunity
• Providing regulatory support for International Markets RA.
• Coordination of assigned regulatory activities.
How you’ll spend your day
1. Document Management and Administrative Support
• Provide support for Certificate of a Pharmaceutical Product (CPP) requests across global and local markets.
• Manage requests for authorizations, certifications, and other regulatory documents; initiate requests as needed.
• Handle documentation requests from manufacturing or operational sites.
• Maintain and update trackers for ongoing regulatory projects and submissions.
• Develop and manage databases for regulatory updates, ensuring timely communication of new requirements or changes.
• Generate and compile reports from internal systems to support regulatory activities and decision-making.
2. Regulatory Systems and Data Management
• Monitor and update market-specific regulatory changes in designated platforms.
• Upload and archive regulatory correspondence in relevant systems.
• Verify and match documents within content plans to ensure completeness and compliance.
• Oversee registration data management activities, with responsibilities evolving as processes develop.
• Maintain accurate documentation in Veeva Vault and other regulatory IT systems.
3. General Regulatory Support
• Complete designated projects and tasks supporting international regulatory affairs, following internal procedures and under guidance from management.
• Coordinate, prioritize, plan, and monitor tasks related to assigned regulatory activities, ensuring alignment with timelines and business objectives.
• Develop and maintain subject matter expertise, proactively solving routine regulatory issues and escalating complex matters as appropriate.
• Communicate effectively with internal teams across regions and with external stakeholders.
• Guide and support junior team members, fostering knowledge sharing and professional development.
• Fulfill other allocated department duties and ad-hoc tasks as directed by senior staff.
• Complete assigned trainings in the internal learning management system within defined timeframes.
• Attend team meetings and provide regular updates on assigned activities and tasks.
Candidate Profile
• Masters in Pharmacy or Masters in Science/Life Sciences
• College or University degree or equivalent work experience that provide knowledge of and exposure to fundamental theories, principles and concepts.
• 8-10 years of experience in the Pharmaceutical Industry, ideally within Regulatory Affairs but R&D, Development or QA would be considered.
• Experience of regulatory documentation within Europe and/or International Markets.
Additional Information
Experience : 8-10 years
Qualification : MPharm, MSc
Location : Bangalore, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 25th January 2026
Mgr Regulatory Affairs : Apply here
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