IQC Supervisor
Location: San Jose, CA
Circulation
Overview
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.
Responsibilities
- 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.
Qualifications
- 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
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