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    Senior Process Engineer - Cleveland, United States - Gradbay

    Gradbay
    Gradbay Cleveland, United States

    3 weeks ago

    Default job background
    Description
    This position is a key role in the Injection Molding, Devices, and Biosurgery Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects.

    Additional focus will also be on manufacturing equipment reliability and process support work within the Injection Molding, Devices, and Biosurgery Operations.

    Cross-functional project management will be involved in this role as well.

    Your team:
    Baxter's employees are united in a mission to save and sustain lives.

    We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies.

    We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.

    What we offer from Day One
    Medical, Dental and Vision coverage
    160 hours of Paid Time Off and Paid Holidays
    401K match
    Paid Parental Leave
    Tuition Reimbursement

    What you'll be doing:
    Design/modify precision assembly and/or manufacturing equipment.
    Manage multiple projects with minimal supervision.
    Prepare estimates for various tasks and projects.
    Manage capital projects both directly and through coordinating engineers.
    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.

    Equipment life cycle management including:
    upgrades, replacement, and decommissioning

    Product life cycle management including:
    product design changes, material changes, Supplier Notice of Change (SNC) assessments, specification changes, etc.
    Provide technical support/troubleshooting to all plant departments.
    Demonstrate proactive communication and problem solving.
    Responsible for supporting and achieving Value Improvement Projects (VIP's).
    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.

    What you'll bring:
    Bachelor's Degree in Engineering Required (Mechanical, Industrial, Electrical, or Computer degrees are preferred)
    5 years or more of Engineering / Manufacturing experience. FDA manufacturing preferred.
    Programming/troubleshooting experience with automation controls, automated assembly, control systems, PLC's, HMI's, servo's, and vision inspection systems is preferred.
    Design software experience (like AutoCAD, Solid Works, etc.) is preferred.
    Six Sigma Master Black Belt Certification or industry standard equivalent is preferred.

    Plastics experience such as:
    plastic bottle blow molding, plastic component injection molding, liquid silicone molding, or film/tubing extrusion is a plus.
    Project Management skills and experience (including Microsoft Project software) are a plus.
    Lean Manufacturing skills and experience are a plus.

    How to APPLY:
    Click APPLY and one of our team members will be in touch.

    #J-18808-Ljbffr
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