About this role
Quality Engineer II at Agiliti. Location: Kansas or Milwaukee or California. Role: supporting quality, resolving issues, leading validations Requirements: BS in engineering or related field, 3+ years design-quality experience in ISO13485/FDA 21CFR820 regulated medical device environments; experience with risk management, DFMEA/Process FMEA, SPC/CPk, FAI/Gage R&R, and design verification/validation. Category: Engineering Seniority: Mid Level Tools: Microsoft Office, Microsoft Project, Microsoft Visio, SolidWorks, Autodesk Commitment: Full Time Workplace: Remote Languages: English