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IQC Supervisor

Location: San Jose, CA



Supervise an inspection team responsible for routine inspections, first article inspections, identifying non-conformance trends, and documentation review. Provide analysis and support for incoming, inprocess, and final inspection/testing. Lead Kaizen activities to improve IQC process flow.



  • Supervise the IQC Inspection team
  • Ensure proper workflow for routine inspection, first articles, non-conformances, finished
  • goods testing, and documentation reviews
  • Analyze key processes and eliminate waste in the processes listed above
  • Perform trending of NCR and identify solutions to prevent recurrence
  • Generate tracking metrics for !QC and provide analysis of the results
  • Provide guidance, training, and instructions for inspectors
  • Create document change orders
  • Data entry and filing including computerized MRP transactions
  • Perform internal calibrations.


  • Experience in a medical device, FDA QSR regulated industry, including ISO 13485
  • requirements
  • Experience inspecting electronics, mechanical and cabled assemblies, as well as printed
  • material and labeling
  • IPC 610 & 620 or equivalent experience
  • ANSI 21.4 Sampling Plans or equivalent experience
  • Experience using Excel, Word, Access
  • Experience using optical inspection systems
  • Strong communications and interpersonal skills
  • Ability to work independently with little supervision
  • Experience training and instructing others
  • Experience handling nonconformance's
  • Minimum of 5+ years related experience in medical device industry
  • Bachelor degree or equivalent
  • 5+ years of experience in inspection and testing experience in the Medical Device Industry
  • Minimum of 3 years of experience in a supervisory position