Senior Regulatory Affairs Associate At Novartis Pharmaceuticals
Job Description
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.
Minimum requirements
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
Division
Global Drug Development
Business Unit
REG AFFAIRS GDD
Country
Egypt
Work Location
Cairo
Company/Legal Entity
NOV PHARMA EGY
Functional Area
Research & Development
Job Type
Full Time
Employment Type
Regular
Shift Work
No