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    Senior Automation Engineer - Cleveland, United States - Insight Global

    Insight Global background
    Description

    Must haves:

    Read all the information about this opportunity carefully, then use the application button below to send your CV and application.
    • 2+ years of programming/troubleshooting experience with automation controls, automated assembly, control systems, PLC's, HMI's, servo's, and vision inspection systems.
    • Experience with Allen Bradley PLC's & HMI's is required.
    • Experience working in GMP facility.

    Plusses:

    • Experience with Magnemotion conveyor system, ultrasonic welding, Staubli robots, Nordson liquid dispensing
    • Design software experience (like AutoCAD, Solidworks, etc.)
    • Lean Manufacturing skills and experience

    About the Position:

    A healthcare client is looking for an Automation Engineer to join their growing team in Cleveland, MS. This position is a key role in their device focus factory and the primary focus will be on a new business startup. The initial project work to bring a new device production line will include –

    • Installation/commissioning/debug of multiple new automated device assembly machines into existing cleanroom space.
    • Provide / support equipment improvements within Baxter's change control process.
    • Validation/Qualification activities for new assembly equipment and ancillary equipment.
    • Assist Project Manager with required project planning, project controls, and procurement work.

    Additional Duties and Responsibilities:

    • Design/modify precision assembly and/or manufacturing equipment.
    • Prepare estimates for various tasks and projects.
    • Drive Continuous Improvement Activities.
    • Interface with plant and corporate groups as well as contractors and vendors.
    • Manage start-up, debug, and commission of new manufacturing processes.
    • Provide technical support/troubleshooting for new device production line.
    • Demonstrate proactive communication and problem solving.
    • Responsible for adhering to FDA Design Control standards at all times.
    • Responsible for adhering to and maintaining all department Standard Operating Procedures (SOPs), forms, and log books.
    • Generate technical documents, reports, equipment specifications, and interpret technical drawings/schematics

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