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Step into the role of Senior Quality Assurance Specialist, where you'll leverage your extensive experience to ensure adherence to the highest quality standards and regulatory compliance within the dynamic field of medical devices. As a key player, you'll spearhead initiatives aimed at driving innovation and advancing patient care through meticulous attention to detail and a commitment to excellence.
The Engineering Manager will be an integral leader at my client's manufacturing shop near Brookfield, managing production from customer contact all the way to final product. This role will report directly to the President and will be heavily involved in organizational decision making.
The Sr. Quality Engineer will sit on the quality team out of the location near Lisle, IL. This role will work closely with the Quality Manager to drive continuous improvement in product and processes, leveraging strong skills in both quality and mechanical engineering.
As the Mechanical Engineer II, you will be responsible for leading the development of innovative products and accessories for the medical device space. You will design, build, and test new products from concept through to production.
In this role you will be overseeing and implementing quality control processes to ensure compliance with regulatory standards and maintain product excellence. Responsibilities include developing and implementing quality management systems, conducting risk assessments, and collaborating with cross-functional teams to address quality issues and drive continuous improvement.
The Mechanical Engineer lll will be a hands-on technical contributor, mainly focused on Class lll medical devices. In this role you will help lead the development of new products, working on design and testing of new devices.
The Senior Quality Engineer will enhance awareness, visibility, and communication regarding quality initiatives while supporting departmental, functional, and corporate quality goals within a medical device manufacturing space. The ideal candidate will possess a robust understanding of FDA/ISO 13485 Quality System requirements, GxP standards, and other pertinent regulations.
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