Company: Global Channel Management,Inc
Location: San Jose
Posted on: January 15, 2022
Quality engineer needs 3 -4 years of quality engineering
experience in FDA regulated medical device manufacturing
Quality engineer requires:
Experience with creating and reviewing of non-conforming material
reports is required
Knowledge of QSR and ISO 13485.
Knowledge of an electronic system for managing Non-Conformances/
CAPAs is preferred.
Competent using office software including Database management, MS
Word, Excel, Internet Explorer, PowerPoint, Visio and Outlook.
Quality engineer duties;
Work with cross functions to ensure that non-conformances and
deviations are accurately and properly initiated, investigated,
documented, reviewed, and approved.
Follow up with Quality Engineering, Supplier Quality Engineering,
Manage non-conforming material movements and complete transactions
in ERP system.
Track and trend Non-Conformance and other Quality Metrics
Keywords: Global Channel Management,Inc, San Jose , Quality engineer, Engineering , San Jose, California
Didn't find what you're looking for? Search again!