Quality Assurance Specialist
October 23
Description
• 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
Requirements
• QC/ QA in pharmaceutical industry/ biotech with environmental monitoring • Collaborating across boundaries • Continuous Learning • Dealing With Ambiguity • GMP Procedures • QA (Quality Assurance) • Quality Control (QC) Testing • Quality Standards • Self Awareness • Technological Expertise • Technological Intelligence
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