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 setting, 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 closure
- Facilitate cross-functional root cause analysis using objective evidence
- Lead CAPA reviews and escalate overdue activities, constraints, and risks




- Coordinate corrective and preventive action plans and effectiveness criteria
- Maintain visibility of commitments and follow up with action owners

Requirements:

- College diploma in engineering, quality, science, or related technical discipline
- At least three years of hands-on CAPA management experience
- Experience managing CAPA from intake through effectiveness verification and closure
- Ability to facilitate cross-functional root cause analysis
- Familiarity with ISO 13485 is an asset

Apply CAPA coordination, investigation planning, and root cause analysis skills to support NDI’s medical device quality systems.

📌 Quality Coordinator CAPA Management (London)
🏢 NDI (Northern Digital
📍 London