Key responsibilities

• Coordinate the day-to-day operation and continual improvement of the QMS
• Coordinate the risk-based internal audit programme, including findings and corrective actions
• Coordinate CAPA, complaints and non-conformances, including root cause and effectiveness reviews
• Manage document control, quality records and quality metrics
• Support compliance with ISO 13485 and MDSAP
• Provide quality evidence and support to Regulatory Affairs
• Coordinate supplier quality activity and monitor emerging quality risks
• Support quality training and provide practical guidance to colleagues
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