Require Pharmacovigilance Associate at Teva | M.Pharm, B.Pharm

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. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.

Post : Pharmacovigilance Associate II

Job Description
• Preparation of Periodic Drug Adverse Experience Reports (PADERs) submitted to the FDA
• Safety analysis of cases identified in the reporting period for Teva’s FDA approved products
• Preparation of responses to requests from regulatory agencies, as required
• Assurance that all tasks are performed in line with relevant procedures
• Cooperation with other groups within Teva Periodic Reports and Risk Management Centre, US Pharmacovigilance, Members of the Global Regulatory Operations Team, Members of the Global Regulatory Affairs Team, and other relevant groups within and outside of Teva Pharmacovigilance Unit
• Training and mentoring of newcomers, as needed
• Responsible to complete all training and SOP/WI reviews in a timely manner
Candidate Profile
• M.Pharm/MDS with 4-6 years of experience
• B.Pharm/BDS with 5-7 years of experience

Additional Information
Experience : 4-7 years
Qualification : B.Pharm/BDS; M.Pharm/MDS
Location : Bangalore
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 28th February, 2021