The Purpose of the Validation expert role is to support Site Manufacturing Science & Technology (MS&T) by providing expertise in process and cleaning validation for aseptic Drug product manufacturing
Job Summary
The Purpose of the Validation expert role is to support Site Manufacturing Science & Technology (MS&T) by providing expertise in process and cleaning validation for aseptic Drug product manufacturing.
Prepare and maintain validation documentation, including process validation protocols and reports, risk assessments, and cleaning validation protocols and reports, in alignment with the Site MS&T team.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Matching Summary
The Purpose of the Validation expert role is to support Site Manufacturing Science & Technology (MS&T) by providing expertise in process and cleaning validation for aseptic Drug product manufacturing.
Skills & Requirements
Must-have
Aseptic Drug Product Manufacturing
Process and Cleaning Validation
Technology Transfer
cGMP Compliance
Quality Management System
Nice-to-have
Applied Statistics
Data Analytics and Digital
Operational Excellence Principles
Effective Stakeholder Engagement
Resilience and Risk Management
Key Requirements
Bachelor's/Master’s degree in Pharmacy, Biotechnology, Chemistry