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.