Let’s figure out what’s next together. If you ask us, this job looks pretty great. Kelly® Professional & Industrial is looking for  a Document Control Assistant  to work at a leading medical device manufacturing facility in Greenville SC (please note: this is an in-person position). You owe it to yourself to consider this great new opportunity. 

Why you should apply to Document Control Assistant:  

• Opportunity to work with one of the best-known and most respected healthcare companies  
  

• Access to outstanding Kelly perks via https://www.mykelly.us/us-mykelly/perks/ 
  

• Monday- Friday 8 AM – 5 PM
  

• 6 month contract role with the possibility of extension

The Documentation Control Assistant is responsible for management of the site document control and records management system..

• Process Greenville documents in GDMS to include reviewing, routing, promotion of effective documents, copying and distributing copies.
  

• Maintain the Annual SOP Review Process, which includes sending monthly notifications of SOPs to be reviewed, issuing periodic SOP status reminders and completing monthly reports.
  

• Manages process for review of global document updates to ensure local changes are made as necessary to maintain compliance with the global Quality Management System.
  

• Provide administrative support for external audits and as needed for the Quality Systems group.
  

• Coordinates the record retention and destruction process.
  

• Site administrator for electronic document management system.
  

• Reviews document content and edits as necessary to ensure compliance.

This job might be an outstanding fit if you: 

• Have an Associate’s Degree 
  

• Bachelor Degree preferred
  

• Previous experience in Document control
  

• Previous experience in regulated environments such as quality or regulated labs.
  

• Must be proficient in Excel and Word
  

• Familiar with medical device production standards

Apply Today!

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