Quality Manager

• Maintain and continuously improve a robust Quality Management System compliant with ISO 9001:2015 and ISO 13485.
• Act as Management Representative, reporting on quality system performance and compliance to senior leadership.
• Lead internal audits, CAPA processes and Management Review activities.
• Design and implement systems for ongoing production quality monitoring and control.
• Analyse quality data and trends, producing clear reports to support decision‑making and resource allocation.
• Partner with production and engineering teams to implement new testing criteria, inspection methods and assembly processes.
• Establish and maintain product, process and raw material quality standards, working closely with suppliers as required.
• Oversee in‑process and final product inspection activities, including dimensional, visual and functional checks.
• Manage customer complaint handling and medical device reporting systems, ensuring effective corrective actions.
• Lead APQP, PPAP and validation activities (IQ/OQ/PQ) for new and transferred projects.
• Manage and develop supplier quality processes and performance.
• Supervise and develop the Quality team, including performance management, training and day‑to‑day direction.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.