About this role
Design Quality Engineer at TAE Technologies. Location: Irvine, California, United States. Role: authoring documents, creating tests, executing tests Requirements: BS in technical or life science,5+ years in medical device quality systems (ISO 13485,21 CFR 820),strong technical writing,test planning,verification/validation experience,MS Office proficiency,and ability to travel up to 90 days/yr. Category: Engineering Seniority: Senior Level Tools: Microsoft Office Commitment: Full Time Workplace: Onsite Languages: English