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The Quality Engineer (Medical Device) will lead quality initiatives in a highly regulated, precision manufacturing environment, ensuring compliance with ISO 13485 and FDA 21 CFR Part 820 while driving continuous improvement across processes and systems. This position offers a clear path to advancement, and offers outstanding development opportunites.
The Quality Engineer will lead quality initiatives in a highly regulated, precision manufacturing environment, ensuring compliance with ISO 13485 and FDA 21 CFR Part 820 while driving continuous improvement across processes and systems. This position offers a clear path to advancement, and offers outstanding development opportunites.
Driving impactful, technical projects which improve product quality, and lower production costs. Improve productivity while ensuring strict adherence to safety, quality, and industry standards.
The Quality Engineer, medical device manufacturing, will work to improve the quality of products and processes while operating in a culture highly receptive to quality. You will have the opportunity to support and provide guidance to ensure adherence to processes and procedures that maintain safety, efficacy, and compliance with applicable standards and regulations onsite at out Hudson, NH facility.
My client is a producer of both temporary and permanent displays for the food and retail industries, and they are seeking an individual ready to advance their career into a leadership role. This position will involve managing and overseeing the quality department at their facility.
Located in Rockford, IL, the Quality Engineer is responsible for ensuring that all manufactured enclosures meet rigorous quality standards. This role involves developing inspection procedures, analyzing production data, and driving continuous improvement efforts. The Quality Engineer works closely with engineering and production teams to ensure compliance with industry regulations and customer requirements.
The Quality Assurance Engineer will lead the implementation and oversight of IATF 16949-compliant systems to ensure product quality and compliance with customer and industry standards. They will drive continuous improvement, manage audits and documentation, and collaborate cross-functionally to resolve quality issues and support new product launches.
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