Quality Engineer II
Core
Develops and implements quality system elements to ensure product compliance with regulations and standards, performing failure analyses and defect investigations.
Role type
Quality Engineer II
Builds
New and existing products in regulated industries
Domain
Medical devices / Regulated industry
Required skills
Quality system implementation, testing and inspection methodology design, failure analysis, statistical techniques, internal audits, QMS adherence, specification revision, cross-functional collaboration
Preferred skills
Medical device industry experience, manufacturing environment experience, Electronic devices and PCBAs experience, familiarity with QSR and ISO regulations
Technologies
MS Word, Excel, PowerPoint
Responsibilities
Collaborate in development and qualification activities for new and existing products, Design and install QC process sampling systems and statistical techniques, Perform failure analyses and defect investigations, Facilitate and perform internal audits, Interface with engineering departments, customers, and suppliers on quality issues, Ensure department adherence to QMS and regulations
Seniority
Mid-level, hands-on IC