This is a 5-month FTCAbout Your New EmployerOur client is a leading manufacturer serving highly regulated healthcare and pharmaceutical markets, working behind the scenes to support the safe and reliable use of critical products.About Your New JobLead key elements of the Quality Management System to ensure compliance with ISO 13485:2016, GMP, and applicable standards, driving continuous improvement.Oversee investigations, customer complaints, non-conformances, and CAPAs, including root cause analysis, corrective actions, and effectiveness monitoring.Coordinate quality activities and projects to meet agreed objectives, providing data analysis, reporting, risk escalation, and updates to the Quality Manager.Support audit readiness and execution, including internal, customer, and regulatory audits, and maintain effective quality system documentation.Manage team performance and daily project delivery while promoting strong cross-functional collaboration and safe working practices.What Skills You NeedThird-level qualification in science or engineering with 3+ years’ Quality Engineering experience in a manufacturing environment.Proven experience working within an ISO 13485:2016 certified manufacturing environment.Demonstrated people management capability with strong planning and coordination skills.Strong quality mindset, promoting continuous improvement and optimization of customer and regulatory processes.
#J-18808-Ljbffr