Quality Assurance Specialist

Manages Quality aspects and projects within area of responsibility • Ensures overall GxP conformity and compliance with Novartis Quality Management Systems • Prepare documentation for batch release of commercial pharmaceuticals • Oversight of all production and testing activities • Supports exception investigations • Review and approval of production, QC, and AS and T records • Executes batch release in compliance with registration • Reporting of technical complaints/adverse events related to Novartis products • Distribution of marketing samples • On-time and GMP-compliant release of dosage forms • Successfully supports continuous improvement projects