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You will enhance and maintain the Quality Management System by leading corrective actions, audits, supplier oversight, risk analysis, and process improvements. The role involves tracking quality metrics, supporting cross-team risk assessments, and ensuring adherence to key regulatory standards.
The Customer QM at an electronics manufacturer ensures that products meet customer expectations by overseeing quality assurance processes, addressing complaints, and implementing corrective actions. They act as the key liaison between customers and internal teams to drive continuous improvement and maintain high satisfaction levels.
As the Sr QE you will maintain and enhance the Quality Management System-managing document control, driving CAPA investigations through root cause analysis and verification of effectiveness, and supporting both internal and external audits. You will also analyze quality performance metrics, collaborate across teams to address non-conformances and supplier issues, and lead process improvement initiatives to ensure compliance with ISO 13485.
The Quality Engineer, medical device manufacturing, will work to improve the quality of products and processes while operating in a culture highly receptive to quality. You will have the opportunity to support and provide guidance to ensure adherence to processes and procedures that maintain safety, efficacy, and compliance with applicable standards and regulations onsite at out Hudson, NH facility.
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