Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
How you’ll spend your day
• Data retrieval for authoring and preparation of selected PSUR sections.
• Review/QC of the data retrieval procedure and selected PSUR sections.
• PSUR finalization (creation of PSUR pdf).
• Drafting responses to requests from regulatory agencies, as required.
• Making sure assigned PSUR-related activities are performed in line with working procedures.
• Collaborative working relationships with other functions in Teva.
Your experience and qualifications
• University degree (B.Pharm, M.Pharm, Pharm.D)
• Active knowledge in English, both written and spoken
• Working experience with databases (e.g. ARISg, Argus, Cognos, Veeva, TrackWise, QlikSense)
• MS Office skills (Word, Excel, PowerPoint)
• Minimum 1-2 years of experience in Pharmacovigilance (PSUR/RMP/PADER writing or ICSR/case processing writing)
• Strong sense for compliance and deadlines.
- Location: Bangalore, India, 560064
- Job Id: 57209