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The Manufacturing/ NPI Engineer will be a key player in the development of essential medical device products through design development into manufacturing through the entire product life cycle phase.
The Design Quality Engineer will play a critical role in ensuring that medical devices meet regulatory and quality standards throughout the product development lifecycle. This position involves collaborating with cross-functional teams to identify design risks, implement process improvements, and maintain compliance with ISO and FDA regulations.
The NPI Engineer will be a key player in the development of essential medical device products through design development into manufacturing through the entire product life cycle phase.
The manufacturing engineer position develops and recommends cost-effective manufacturing processes and methods in accordance with product specifications and quality standards; recommends improvements to production processes, methods and controls; helps to coordinate manufacturing launches for new or revised products. Helps to troubleshoot equipment and determine the root cause of the equipment failure as needed throughout the plant.
My client is a global manufacturer for the medical device industry and are seeking a Senior Quality Manager to come on and lead their quality department for this facility. This is an opportunity to work for a leading manufacturer in the industry and to grow your career.
The Quality Engineer (medical device manufacturing) will lead efforts to ensure product compliance with medical device regulations and quality standards, focusing on design controls, risk management, and validation activities at our Southborough, MA facility. They will collaborate cross-functionally to drive continuous improvement, resolve complex quality issues, and support the seamless transition from design to manufacturing.
This position is for a talented Embedded C++ Software Engineer to join an industry leading medical device organization just south of Boston to help lead and shape the future of their software engineering division, whilst working on some revolutionary medical devices.
The SQE at my client is responsible for developing, implementing, & maintaining quality systems that meet certification and customer requirements. This role involves creating quality control instructions, conducting root cause analyses, and supporting continuous improvement initiatives to ensure product conformity and process efficiency.
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