Position Title
Head RA GDD Sandoz & IM
16-Mar-2020
Job ID
292092BR
Job Description
Responsible and accountable for ensuring local product registration and pricing approval with the Drug Regulatory Authority and to facilitate and/or expedite all regulatory based approvals. Coordinate with regional/ global Regulatory Affairs leads. Responsible for responding to Health Authorities (HA) in issues pertaining to Novartis’ products and licenses, providing regulatory intelligence to general management and support other functions as and when required. Additionally, to act as CPO RMP Manager.
Minimum requirements
B.Pharmacy preferably with Masters Degree in Pharmaceutical or Management Sciences English 8-10 years or more experience in Regulatory Affairs
Job Type
Full Time
Country
Pakistan
Work Location
Karachi
Functional Area
Research & Development
Division
Global Drug Development
Business Unit
REG AFFAIRS GDD
Employment Type
Regular
Company/Legal Entity
Novartis Pharma (Pakistan) Ltd
Shift Work
No
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