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Quality Engineer with experience supporting medical device manufacturing operations, ensuring compliance with FDA, ISO 13485, and customer quality requirements through robust quality systems, risk management, and continuous improvement initiatives. Skilled in root cause analysis, validation activities, CAPA management, and cross-functional collaboration to drive product quality, regulatory compliance, and patient safety.
We are seeking a Quality Engineer to support customer quality, inspections, corrective actions, and continuous improvement initiatives throughout the facility. This individual will play a critical role in maintaining quality standards, resolving customer concerns, and driving process improvements while serving as a key liaison between customers and manufacturing operations
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