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QA Specialist
Ref No.: 18-03438
Location: Waukegan, Illinois
Job Duties:
  • Update component files with supplier documentation/scanning of documentation
  • Validate regulatory data on new and existing components
  • Qualify new components being requested for patient recovery
  • Medical product FDA regulatory background required
  • Background with UDI preferred
  • Registration of medical products with the FDA, highly preferred
  • Strong Microsoft office and excel skills proficient with query writing and use of macros.
  • Strong written and verbal communication skills
  • Ability to communicate within all levels of CAH regulatory organization including Sr leadership