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QA Document Control Coordinator

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Internationally recognized Biopharmaceutical Company is looking to identify and hire a QA Document Control Coordinator on a contract basis.  This is a great opportunity to gain professional development.

 

The QA Document Control Coordinator will be responsible for, but not limited to:

  • Compiling and maintaining control records relating to label issuance.
  • Printing production labels for manufacturing (managing work schedules).
  • Assembling Lot Folders for all departments (managing work schedules).
  • Verifying of all documents prior to lot folder assembly.
  • Maintaining inventory of all label and ribbon stocks.
  • Supporting the Document Control program.

Requirements:

  • A minimum of two (2) years administration experience in a Quality Assurance Document Control medical device manufacturing environment or equivalent.
  • Experience with Weber Labeling Systems preferred.
  • Graphic design knowledge a plus.
  • Ability to speak, read, and write English.
  • Good oral and written communication skills.
  • Proficient in Word, Excel, PowerPoint, Outlook.