The HUB Labeling Manager will be responsible for preparation of labeling documents and updating them timely according to internal SOPs and external regulatory requirements
Job Summary
The HUB Labeling Manager will be responsible for preparation of labeling documents and updating them timely according to internal SOPs and external regulatory requirements.
This role acts as a Subject Matter Expert on local, regional and multi-country regulatory labeling requirements and supports digital transformation projects focused on label development and approval.
Pfizer is committed to a diverse, inclusive, and flexible workplace culture that supports employee work-life harmony and disability inclusion.
Matching Summary
The HUB Labeling Manager will be responsible for preparation of labeling documents and updating them timely according to internal SOPs and external regulatory requirements.
Skills & Requirements
Must-have
Regulatory labeling document preparation
Global Document Management System (GDMS)
Labeling tracking system management
Regulatory knowledge application
Quality control of labeling documents
Use of MS Excel and SharePoint
Digital solutions for label development
Nice-to-have
Multi-language skills
Project management skills
Cross-cultural collaboration
Problem-solving skills
Attention to detail
Experience with process automation and machine learning
Strong written and verbal communication
Key Requirements
Life sciences or pharmacy graduate or equivalent experience
Experience in Regulatory Affairs registration and commercialization activities
Fluency in English
Knowledge of global and local regulatory guidelines
Ability to manage regulatory implications of product strategy
Demonstrated project management and problem-solving skills