Head RA GDD Sandoz & IM
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.
B.Pharmacy preferably with Masters Degree in Pharmaceutical or Management Sciences English 8-10 years or more experience in Regulatory Affairs
Research & Development
Global Drug Development
REG AFFAIRS GDD
Novartis Pharma (Pakistan) Ltd
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