Quality Engineer, Medical Devices & Validation

Location: Fenimore

A leading medical device company located in New York is seeking a Quality Engineer to support and maintain their Quality Management System (QMS). This role involves regulatory compliance, validation activities, and internal audits while partnering with various teams to improve quality and operational processes. The ideal candidate will have 5–7 years of experience in regulated manufacturing, with strong knowledge of cGMP and ISO standards.

A Bachelor's degree in a relevant field is preferred.

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