On-Site Process Quality Engineer — Med Device & CAPA

A leading health technology company in Bedford, MA, is seeking a Process Quality Engineer to ensure high-quality performance and compliance in manufacturing processes. The role requires a minimum of 5 years in FDA regulated environments, with experience in CAPA processes and mentoring engineers. The Process Quality Engineer will lead validation protocols, manage nonconformance events, and drive continuous improvement initiatives. This position requires onsite work at least 3 days a week, offering a competitive salary between $102,480 and $163,968 along with comprehensive benefits.
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