Job Description :
Role – ETQ Specialist
Location – Irvine, CA
Duration- Long Term
Phone and Skype
Minimum 3+ years’ experience in ETQ admin tasks as a Medical device industry quality Engineer including CAPA management, NC management and Audit observation management and admin support in ETQ.
A bachelor’s Degree in Engineering or equivalent is required.
A Mechanical Engineering degree is preferred
Knowledge of Medical device Industry process
Knowledge on Quality Management, Pull records from ETQ, Metrics and trending, report generation for Audit preparedness
Knowledge on Quality Compliance
Knowledge on ETQ and QlikSense
Must possess good communication skills (verbal and written), familiar with project management methodology, problem solving, and presentation skills
Roles & Responsibilities
Provide administrator support for EtQ and running reports in QlikSense and provide support to pull historical records from REACT, ATMS, CURVE, Prism, and Unity/EDL.
Modification of designated ASP NC/CAPA/OBS
Creation of metric reports, generation of CAPA/NC/OBS summary reports for ASP records
Providing designated ASP historical records
Other activities mutually agreed upon between Buyer Contracting Party and Supplier Contracting Party