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.
