GMP Document Coordinator

Found in: Appcast Linkedin GBL C2 - 3 weeks ago


Morristown, United States KellyMitchell Group Full time

Job Summary:

Our client is seeking a GMP Document Coordinator to join their team in Morristown, New Jersey The selected candidate will assist the Clinical Supply Manager with developing records and executing records to prepare study medication.


Duties:

  • Scan and file documents into an electronic system
  • Appropriately name each document and file the document into the system
  • Prepare shipments, issue FedEx Labels, and track shipments
  • Handle returned study medication and prepared for storage
  • Monitor expiration dates
  • Maintain inventory of secondary packaging material


Desired Skills/Experience:

  • Must have previous experience in cGMP environment
  • Experience with cGDP is a plus


Benefits:

  • Medical, Dental, & Vision Insurance Plans
  • 401K offered


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