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The Quality Engineer position with my client involves ensuring compliance with medical device regulations, particularly ISO 13485 and FDA standards, to maintain the highest quality standards in organ preservation and transplantation technologies. The role requires proactive problem-solving, collaboration with cross-functional teams, and a commitment to continuous improvement to uphold my clients' mission of advancing organ transplantation technology.
The Design Quality Engineer role involves ensuring the quality and compliance of medical device designs, particularly in organ preservation and transplantation. Candidates will apply expertise in quality management systems and regulatory standards to drive product safety and efficacy in this critical healthcare field.
A Quality Engineer will be responsible for ensuring product quality by applying statistical analysis and quality control methodologies in precision manufacturing. This candidate will collaborate with cross-functional teams to address and prevent quality issues, emphasizing continuous improvement and adherence to high-quality standards.
The Quality Engineer will be responsible for ensuring adherence to quality standards and procedures in the design, manufacturing, and testing processes of power components and systems. They employ methodologies such as Six Sigma and Statistical Process Control to drive continuous improvement and ensure product reliability and performance.
The Quality Engineer position requires a Bachelor's degree in engineering, accompanied by proficiency in quality management systems and a deep understanding of industry standards and regulations. Candidates should possess strong problem-solving and analytical skills, alongside excellent communication and teamwork abilities.
Our client is a manufacturer of metal machined components serving the medical device industry. Their product is used in critical devices and quality is at the forefront of everythingn they do. With their developed team, they are looking for a senior level quality engineer to lead both internal and external projects.
The Quality Engineer 3 position with my client involves ensuring adherence to quality standards and regulatory requirements in the production of medical devices and pharmaceutical products. Responsibilities include conducting quality assessments, implementing corrective actions, and collaborating cross-functionally to drive continuous improvement in product quality and reliability.
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