Coordinate CAPA management at NDI, supporting medical device quality through root cause analysis and evidence-based investigations. Hybrid work may be available where responsibilities allow.As a Quality Coordinator, you will support product release, quality investigations, audit readiness, and Quality Management System improvements. You will work across teams in a regulated medical device workplace, coordinating corrective and preventive actions from intake through closure. Your work helps ensure products meet established quality and regulatory requirements before reaching customers.Key Responsibilities:Coordinate CAPA intake, investigations, documentation, verification, and closureFacilitate cross-functional root cause analysis using objective evidenceLead CAPA reviews and escalate overdue activities, constraints,



and risksCoordinate corrective and preventive action plans and effectiveness criteriaMaintain visibility of commitments and follow up with action ownersRequirements:College diploma in engineering, quality, science, or related technical disciplineAt least three years of hands-on CAPA management experienceExperience managing CAPA from intake through effectiveness verification and closureAbility to facilitate cross-functional root cause analysisFamiliarity with ISO 13485 is an assetApply CAPA coordination, investigation planning, and root cause analysis skills to support NDI's medical device quality systems.

📌 Quality Coordinator Capa Management (Alton)
🏢 NDI (Northern Digital
📍 Alton