QA Specialist, DHR for Medical Devices

Philips Iberica SAU is seeking a Quality Assurance Specialist for Device History Record in Cambridge, Massachusetts. This role is vital in ensuring compliance with regulatory and internal standards for medical device manufacturing. Responsibilities include reviewing records for accuracy and collaborating with quality engineering teams. Candidates should have 1+ years of relevant experience and a background in Good Documentation Practices and quality management systems. The position requires full-time, on-site presence and offers a competitive hourly wage and comprehensive benefits package.
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