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    ME-Galway

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    Juliano Muniz
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    ME-Galway

    Uploaded by

    Juliano Muniz
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    © © All Rights Reserved

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    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
    10 views2 pages

    ME-Galway

    Uploaded by

    Juliano Muniz
    1

    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
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    Job Overview

    The Manufacturing Engineer will report to the Engineering Supervisor and will be responsible for
    providing engineering support to Manufacturing (Automated Injection Moulding Cell / Welding /
    Ablation business). You will also be responsible for the continuous improvement activity required to
    ensure that the process is capable and delivering results in line with the agreed KPI’s.

    Responsibilities:

     Health & Safety: Ensure that all Health, Safety and Environmental requirements are fulfilled
    for the manufacturing process.

     Quality: Drive Engineering solutions to ensure Right First-Time principles, driving yield
    improvements, Complaint reductions and supporting the CAPA process.

     Continuous Improvement: Own the manufacturing process, work with key business
    stakeholders and operations teams to assess process capabilities, prioritize process
    improvement opportunities implementing them using Lean and six-sigma tools.

     Service: Drives a culture of Exceptional Customer Experience (ECE) for both the Internal and
    External customers, by ensuring that projects and commitments and continually being met
    or exceeded.

     New Product Introduction: Supports New Part Introduction in conjunction with the
    Prototyping / NPD Group.

     Responsible for managing the overall equipment performance (OEE) through the appropriate
    use of Lean Manufacturing tools and techniques (TPM etc)

     Ensure equipment preventative maintenance procedures are effective and ensure


    compliance to preventative maintenance program.

     Introduction of new equipment; equipment installation validation (EIQ,EOQ), process


    development and validation (OQ , PQ).

     Resolve quality and technical issues such that impact on product supply to customers is
    minimized and support Business Unit CAPAs, NCs, FMEAs and audit prep activities.

     Develop and manage SOPs / manufacturing standards / operations standard work as


    required in compliance with change control process.

     CAPEX management for new and replacement equipment, including investigating in state-of-
    the-art process technologies and evaluating potential competitive advantage and the cost
    benefit of introduction.

     Maintain high quality / compliance standards in line with Medical Devices manufacturing
    requirements within Creganna.

     Manages external relationships with key technology providers.

     Manage a variable workload to meet operational requirements.

    Candidate Desired Profiles:

     Engineering level 8 degree in Polymer Technologies, or equivalent qualification.


     Preferably a minimum of 3 years’ experience in a similar Engineering level role.

     Medical Device experience would be an advantage.

     Demonstrate a practical understanding of Lean Manufacturing principles and statistics.

     Injection Moulding experience required.

     Demonstrate operating knowledge of Minitab software, would be an advantage.

     SolidWorks /AutoCAD skills would be an advantage.

     Demonstrate a dynamic, motivated & flexible approach to work with results-oriented


    attitude.

     Excellent communication, planning and organizational skills.

     Knowledge of ISO & FDA compliance.

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