Join the QA compliance team and help ensure robust compliance, monitor key quality indicators (KQI) and effective implementation of the Novartis Quality Management System
Job Summary
Join the QA compliance team and help ensure robust compliance, monitor key quality indicators (KQI) and effective implementation of the Novartis Quality Management System.
You will act as a site subject-matter expert in your designated area such as data integrity, audit and inspection management, deviation investigations partnering closely with multiple departments and external partners.
Through your contributions to investigations, CAPAs, audits and inspections, and continuous improvement, you will strengthen compliance, make a meaningful impact across our operations and for the people relying on our medicines.
Matching Summary
Join the QA compliance team and help ensure robust compliance, monitor key quality indicators (KQI) and effective implementation of the Novartis Quality Management System.
Skills & Requirements
Must-have
cGxP compliance monitoring
Quality Management System implementation
Deviation and CAPA management
Audit and inspection coordination
Data integrity oversight
Regulatory compliance adherence
Nice-to-have
Collaboration across departments
Effective communication skills
Digital savviness
Problem solving skills
Leadership capabilities
Dealing with ambiguity
Key Requirements
Master’s degree in scientific field
Experience in regulated pharmaceutical environment
Strong understanding of Good Manufacturing Practices