Senior Design Quality Engineer, Medical Devices (QMS)
Regulatory Toolkit
Philips in Bedford, MA is seeking a Senior Design Quality Engineer to lead the design control process for medical devices, overseeing inputs, verification, validation, and design transfer. You will drive process validation, CAPA, risk management, and PMS analytics to ensure regulatory and quality standards are met throughout the product lifecycle. The role requires 5+ years in FDA-regulated environments, strong knowledge of ISO 14971, and a Bachelor’s in quality/engineering. #J-18808-Ljbffr Regulatory Toolkit
Vacancy posted 3 days ago
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