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

EQUAL OPPORTUNITY EMPLOYER - DISABILITY AND VETERAN

#L1-BJ