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The Quality Engineer (medical device manufacturing) plays a key role in ensuring product and process quality through all phases of development, validation, and production, in compliance with ISO 13485 and FDA regulations. This individual will lead root cause investigations, support design controls, and drive continuous improvement initiatives in a fast-paced, innovation-focused environment.
A Project Engineer with 2+ years of experience in commercial and healthcare projects coordinates technical aspects, supports project management, and ensures projects stay on time and within budget. Responsibilities include reviewing designs, managing documentation, overseeing site progress, controlling costs, ensuring quality, and solving technical issues.
The Field Service Engineer will oversee and ensure the highest standards of quality across all automotive products and processes, driving continuous improvement and compliance with industry regulations. They will lead quality control teams, coordinate audits, and implement corrective actions to maintain customer satisfaction and operational excellence.
The Manufacturing Engineer focuses on integrating new projects into production and enhancing existing manufacturing processes to improve efficiency, quality, and ergonomics. It requires strong technical problem-solving, the ability to manage projects independently, and occasional customer interaction to clarify technical requirements.
The Product Development Quality Engineer ensures the highest quality standards for advanced micromanufactured components used in medical devices, focusing on compliance, process improvement, and defect prevention. The role involves collaborating with cross-functional teams to develop and validate robust quality systems, driving innovation in medical device manufacturing.
This Product Development Quality Engineer role involves ensuring adherence to strict quality and regulatory standards throughout product and process lifecycles, leading quality initiatives, and driving continuous improvement. Responsibilities also include technical leadership, mentorship, and collaboration with internal and external stakeholders to guarantee the development of high-quality, compliant medical devices
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