About this opportunity
Prismatik lists this Senior Medical Device QA Engineer – Lead Quality & Compliance opportunity in irvine, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Prismatik in Irvine, CA seeks a Sr. QA Engineer to embed quality across medical device development and manufacturing. You will own CAPA, risk management, validation, and QMS activities, collaborating with R&D, Manufacturing and Regulatory Affairs to ensure safety, performance, and compliance.
You will lead audits, drive continuous improvement, and mentor junior engineers, ensuring process controls meet global standards and patient safety is prioritized.
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Worksite address
irvine, CA, 92713, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.