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Documentation Associate /Quality Specialist

Company: Global Channel Management, Inc.
Location: Irvine
Posted on: July 13, 2019

Job Description:

Documentation Associate /Quality Specialist needs 2 year degree: Science, Chemistry or Biology Documentation Associate /Quality Specialist requires: 2-4 years related experience. Working in a laboratory environment in a pharmaceutical, medical device or related industry including Quality Assurance Ability to work in an ergonomic office setting for most of the working day. Cognizant of others around them Project management multiple projects and priorities. cGMP, ISO, and FDA Requirements General knowledge of pharmacopeias Different computer software such as Microsoft Word, Excel, Access, Visio, Power Point, and Outlook preferred. Computerized systems such Documentum, Trackwise, and SAP preferred but not required. Science (Chemistry or Microbiology) background is preferred to be considered for this role. Documentation Associate /Quality Specialist duties: Assists with word processing Master Specifications and Documentation SOPs as needed. Assists in processing Product Launch Approvals (PLAs) and PLA Amendments as completed documents in CORAL. Effectively communicates (written and verbal) with colleagues at most levels of the organization to achieve timelines for project completion. Keeps project records organized to allow others within the Master Specifications and Documentation department to take over if necessary. Assists the Master Specifications and Documentation department as needed.

Keywords: Global Channel Management, Inc., Irvine , Documentation Associate /Quality Specialist, Other , Irvine, California

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