Manages Quality aspects and projects within area of responsibility and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems
Job Summary
Manages Quality aspects and projects within area of responsibility and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.
Executes batch release in compliance with registration and ensures on-time and GMP-compliant release of dosage forms.
Reports technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt.
Matching Summary
Manages Quality aspects and projects within area of responsibility and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.
Skills & Requirements
Must-have
Quality Assurance and Quality Control
Environmental Monitoring and Cleanliness Zones
Good Manufacturing Practices (cGMP)
Audit and Inspection Management
Release Management
Quality Compliance
Nice-to-have
Collaboration across boundaries
Dealing With Ambiguity
Operational Excellence
Regulatory requirements knowledge
Problem Solving Skills
Leadership
Communication skills
Digital saviness
Data Integrity
Key Requirements
Experience in Quality Assurance and Quality Control