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The Supplier Quality Engineer role focuses on ensuring supplier compliance and driving quality improvements across the supply chain by conducting audits, managing corrective actions, and supporting new product development. It requires collaboration with internal teams and suppliers to maintain standards, reduce risks, and implement continuous improvement initiatives.
The position leads design assurance activities for new product development, ensuring full compliance with FDA, ISO, and global medical device regulations. It drives quality engineering efforts across the product lifecycle, including risk management, verification/validation, and process validation, while supporting cross‑functional teams and suppliers.
This is a high-level Quality Engineering role with a medical device manufacturer located near the Illinois-Wisconsin border. The position is responsible for overseeing all QA/QC activities within a metal fabrication environment.
The Plant Manager will oversee daily operations, ensuring efficiency in production and compliance with safety standards. This role is pivotal in leading the team to achieve operational excellence in the plastics sector.
The Quality Engineer will be responsible for managing quality systems, conducting audits, and leading initiatives such as APQP, PPAP, and continual improvement projects within a precision manufacturing environment. The role requires strong knowledge of automotive quality standards, GD&T, and proficiency with AIAG tools to ensure compliance and customer satisfaction.
The quality engineer will help lead all quality-driven activity associated with the design and manufacturing of precision medical devices and components. The ideal candidate will help lead all audits, handle QA/QC activity, and work cross-functionally with engineering teams to ensure product and customer standards are met.
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