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Responsibilities:

  • Support design reviews, debug, acceptance and validation activities for equipment being developed by external suppliers.
  • Support decommissioning and recommissioning of equipment.
  • Fundamental knowledge of statistical analysis - specifically GR&Rs & Process Capability.
  • Experience with Allen-Bradley/Rockwell Automation programming, Studio5000, RSView ME/SE, Siemens S7 programming, Staubli/EPSON/ABB robot.

Requirements:

  • 4+ years' experience in a medical device manufacturing environment.
  • Strong preference for assembly automation systems experience.
  • Validation experience: IQ, OQ, PQ and TMVs.
  • Automation control systems background – PLCs, HMIs, Vision systems, Servos & Robots.