Job opportunity
Process Quality Engineering Team Lead
Kardium Inc.
Lead process quality engineering at Kardium, applying non-conformance management and root-cause analysis across a two-shift manufacturing operation.
As Process Quality Engineering Team Lead – Operations, you will guide Process Quality Engineers supporting Catheter/Introducer subassembly processes. You will investigate quality issues, disposition non-conforming products, and coordinate rework activities. The position requires collaboration with Quality Control, Engineering, Manufacturing, and Quality Assurance. Kardium develops The Globe® Pulsed Field System for atrial fibrillation treatment and is focused on regulatory approvals and commercial launch.
Key Responsibilities:
Lead Process Quality Engineers across operational and project work
Investigate and disposition non-conforming products and materials
Coordinate rework activities within subassembly processes
Drive systemic product quality investigations and improvements
Report product quality trends and process performance
Requirements:
Bachelor’s degree or higher in science or engineering
At least eight years of engineering experience
Experience in technical, multidisciplinary environments
Knowledge of statistics, SPC, FMEA, and process capability
Experience with non-conformances and root-cause analysis
Apply your leadership, quality engineering, and investigation expertise to support Kardium’s medical device manufacturing operations.
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Apply on source site As Process Quality Engineering Team Lead – Operations, you will guide Process Quality Engineers supporting Catheter/Introducer subassembly processes. You will investigate quality issues, disposition non-conforming products, and coordinate rework activities. The position requires collaboration with Quality Control, Engineering, Manufacturing, and Quality Assurance. Kardium develops The Globe® Pulsed Field System for atrial fibrillation treatment and is focused on regulatory approvals and commercial launch.
Key Responsibilities:
Lead Process Quality Engineers across operational and project work
Investigate and disposition non-conforming products and materials
Coordinate rework activities within subassembly processes
Drive systemic product quality investigations and improvements
Report product quality trends and process performance
Requirements:
Bachelor’s degree or higher in science or engineering
At least eight years of engineering experience
Experience in technical, multidisciplinary environments
Knowledge of statistics, SPC, FMEA, and process capability
Experience with non-conformances and root-cause analysis
Apply your leadership, quality engineering, and investigation expertise to support Kardium’s medical device manufacturing operations.
#J-18808-Ljbffr