Senior Regulatory Affairs Associate At Novartis Pharmaceuticals
Contributes and support the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Supports all registration activities of the Department to ensure compliance with the requisites of the local pharmaceutical regulatory environment.
Project & stakeholder feedback -Product license update in terms of CMC in agreed timeline -Adherence to Novartis policy and guidelines
Operations Management and Execution Project Management Functional Breadth Cross Cultural Experience
Global Drug Development
REG AFFAIRS GDD
NOV PHARMA EGY
Research & Development