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