Quality Engineer: Medical Devices & Regulatory Compliance

A leading technology firm based in Farmington Hills, MI, is seeking a Quality Engineer responsible for ensuring compliance with regulatory requirements and quality standards. The role includes supporting quality assurance activities across product lifecycle stages including design, manufacturing, and validation, as well as managing documentation, audits, and customer complaints. Candidates should possess a relevant Bachelor's degree and strong knowledge of FDA regulations and ISO standards.

This is a pivotal role for maintaining quality in medical device manufacturing.
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