Azurity Pharmaceuticals

Senior Manager, Quality Systems

Azurity Pharmaceuticals

Overview

Role involves leading the Quality Management System and ensuring compliance in a regulated pharmaceutical environment.

Ideal candidate should have 5-7 years of experience in quality assurance and strong knowledge of GxP principles.

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Locations

  • Ireland, Leinster, Dublin

Requirements

  • Bachelor's degree required
  • 5-7 years of experience in documentation management
  • Strong knowledge of GxP principles
  • Proven experience with electronic Document Management Systems
  • Demonstrated leadership and project management skills

Responsibilities

  • Lead development of compliant Quality Management System
  • Oversee validation of electronic quality systems
  • Manage Documentation Management System
  • Develop GxP training strategies
  • Drive continuous improvement initiatives
  • Lead Computer System Validation program
  • Serve as contact for audits and inspections