Teva R&D is inviting Regulatory Affairs Professionals

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.

Teva R&D is inviting Regulatory Affairs Professionals with experience in below skillsets

Regulatory Affairs Associate I/II/III US post approvals
(2-10 years of relevant US post approval experience)
Experience in Change control assessment for US market & post approval activities like annual report,
CBE O.CBE BO and PAS

Regulatory Affairs Associate I Global Regulatory Operations
(2-4 years of experience)
Experience in regulatory data managements pharma domain, regulatory knowledge (US & EU) would be preferred

Regulatory Affairs Associate I/ll EU Market RA Support Team
(2-6 years of experience)
Experience in Regulatory Affairs - knowledge of Blueprint reviews and approvals process, Veeva Vault systems, Office-365 applications.

Regulatory Affairs Associate I/II EU post approvals
(2- 6 years of experience)
Experience in pharma industry ideally in Regulatory Affairs in EU post approvals

Qualification : Degree in science/Life sciences/pharmacy or equivalent qualification
Work Location : Seawoods, Navi Mumbai

Walk in Interview
Date : 22nd Feb 26 from 10 am to 2 pm
Venue : Teva Pharmaceuticals office
C- Wing, 8th floor, Time Square Building, Makwana Road,
Taluka- Gamdevi, Marol, Andheri East, Mumbai- 400059