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Quality engineer

Company: Global Channel Management,Inc
Location: San Jose
Posted on: January 15, 2022

Job Description:

Quality engineer needs 3 -4 years of quality engineering experience in FDA regulated medical device manufacturing environment(s).

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.
Self-directed.
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, Manufacturing
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

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