Quality Manager - Medical Device - Cumberland, RI

Lead investigations involving customer complaints, nonconformances, and CAPAs while driving effective root cause analysis and corrective actions. Manage supplier quality activities and champion continuous improvement, risk management, and process optimization initiatives.

• Lead, maintain, and continuously improve the Quality Management System (QMS) while ensuring compliance with applicable industry standards and regulations.
• Manage internal, customer, and third-party audits while ensuring ongoing audit readiness.
• Oversee product inspection, testing, and release processes to ensure compliance with quality requirements and specifications.
• Lead investigations involving customer complaints, nonconformances, and CAPAs while driving effective root cause analysis and corrective actions.
• Monitor quality performance metrics, prepare reports for leadership, and identify opportunities for improvement.
• Partner with production, engineering, and supply chain teams to strengthen quality performance throughout manufacturing operations.
• Manage supplier quality activities and champion continuous improvement, risk management, and process optimization initiatives.

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.

Lead quality strategy in a regulated medical manufacturing environment.Drive continuous improvement and make a visible organizational impact.

• Bachelor's degree in Engineering, Quality Management, or a related discipline.
• 5+ years of Quality Assurance or related experience, preferably within medical device manufacturing.
• Strong knowledge of ISO 13485, FDA regulations, and other regulated manufacturing standards.
• Experience leading audits, managing quality systems, and ensuring regulatory compliance.
• Strong analytical, problem-solving, and root cause investigation skills.
• Excellent leadership, communication, and cross-functional collaboration abilities.
• Experience using quality management tools, CAPA systems, and continuous improvement methodologies.

Our client is a respected manufacturer operating within a highly regulated industry where quality, precision, and compliance are critical to success. The organization offers a collaborative culture focused on operational excellence, innovation, and ongoing professional growth.

• High-impact leadership role with visibility across the organization.
• Opportunity to shape and improve quality systems and operational performance.
• Collaborative environment with strong cross-functional engagement.
• Work within a quality-focused, highly regulated industry that values excellence.
• Ability to mentor teams, drive change, and build long-term career growth.