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Quality Engineer

In United States

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Quality Engineer   

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JOB TITLE:

Quality Engineer

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

IRVINE United States

JOB DESCRIPTION:

Position Name: Quality Engineer Location: Irvine, CA Duration: Contract / Fulltime Rate: on C2C Minimum Education / Experience Bachelor's degree in a related field, with quality or research and development background in a medical device or other regulated industry is required. Preferred Qualifications   Primary responsibilities include working in Quality Operations or Quality Engineering and with other functional groups in support of new product/process development. Knowledge of GDP, 21 CFR Part 820 (QSR) and ISO 134085 (QMS) requirements Intermediate to advanced knowledge of Microsoft Office including (Excel, Word Paint, Power Point, Publisher, Outlook), also Adobe Acrobat, electronic communication equipment such as scanner, digital camera, and printer. Ability to use (or willing to learn) enterprise resource planning system (JD Edwards One World), and other software as required. Builds and Maintain record of work orders. Also support on work order closure. Ability to work with employees at all levels of the organization and to put at ease the people whose work is being observed and documented. Excellent knowledge of English grammar and excellent written and oral communication skills. Experience in editing procedures written by others to verify accuracy, consistency, grammar and format. Experience in examining documents such as drawings, change orders, and specifications to verify completeness and accuracy of data. Tracks status of documents under revision in a computer database. Initiates Engineering Change Orders, including preparing all applicable documents.

Position Details

POSTED:

Dec 03, 2022

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S16578432916238820

LOCATION:

United States

CITY:

IRVINE

Job Origin:

OORWIN_ORGANIC_FEED

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In Dallas Fort Worth
Aug 19, 2017 9am-6pm
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Position Name: Quality Engineer Location: Irvine, CA Duration: Contract / Fulltime Rate: on C2C Minimum Education / Experience Bachelor's degree in a related field, with quality or research and development background in a medical device or other regulated industry is required. Preferred Qualifications   Primary responsibilities include working in Quality Operations or Quality Engineering and with other functional groups in support of new product/process development. Knowledge of GDP, 21 CFR Part 820 (QSR) and ISO 134085 (QMS) requirements Intermediate to advanced knowledge of Microsoft Office including (Excel, Word Paint, Power Point, Publisher, Outlook), also Adobe Acrobat, electronic communication equipment such as scanner, digital camera, and printer. Ability to use (or willing to learn) enterprise resource planning system (JD Edwards One World), and other software as required. Builds and Maintain record of work orders. Also support on work order closure. Ability to work with employees at all levels of the organization and to put at ease the people whose work is being observed and documented. Excellent knowledge of English grammar and excellent written and oral communication skills. Experience in editing procedures written by others to verify accuracy, consistency, grammar and format. Experience in examining documents such as drawings, change orders, and specifications to verify completeness and accuracy of data. Tracks status of documents under revision in a computer database. Initiates Engineering Change Orders, including preparing all applicable documents.


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