Head RA GDD Sandoz & IM


Job Description

Position Title
Head RA GDD Sandoz & IM


Job ID

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


Work Location

Functional Area
Research & Development

Global Drug Development

Business Unit

Employment Type

Company/Legal Entity
Novartis Pharma (Pakistan) Ltd

Shift Work

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