Manufacturing Engineer 2

Requisition ID 2025-16734
Job Location(s)
Limerick Ireland
Job Locations
IE-Limerick
Languages Required
English
Travel
None
Company
Cook Ireland
Position Type
Full Time
Category
Engineering
Education
Associate's Degree/Diploma

Overview

 
The Manufacturing Engineer 2 will be responsible for key activities across a variety of
manufacturing engineering disciplines, namely New Product Introduction, Process
Improvement, Production Support and Production Maintenance. Key activities will include
leading projects to either introduce or support and improve existing products. More specific
details are listed below for the specific roles.
 
Position:                     Manufacturing Engineer 2, Production Support
                                                                                                                                                       
Reporting to:              Manager, Manufacturing Engineering

Responsibilities

  • Source and install new equipment requirements into manufacturing in accordance
    with Cook Medical’s quality system.
  • Work closely with the Machine Shop to develop jigs, fixtures, and tooling to improve
    Manufacturing efficiencies.
  • Support with defining maintenance and calibration requirements for manufacturing
    equipment both new and improve existing in accordance with Cook Medical’s quality
    system.
  • Prepare, review and approve change orders and other quality system documentation
    requiring manufacturing engineering sign-off.
  • Develop Work Contents for Manufacturing Flow lines by completing Time studies, removing nonvalue add waste and Generating standard of work.
  • Development of project deliverables such as BOM’s and Production Documentation
    (Including IQC and Work instruction creation).
  • Plan and execute improvement projects to ensure that project timelines, quality and
    cost targets are met.
  • Deputise for Manufacturing Engineering Manager/Manufacturing Engineering Team
    Lead

Qualifications

  • Bachelor’s degree is desired, preferably in engineering or a related field and / or relevant experience.
  • Minimum of 3 years’ relevant experience is required.
  • Strong interpersonal and organisational skills and the ability to communicate at all levels of the organisation.
  • Willingness to seek out and drive improvement.
  • Proven project planning skills and the ability to execute projects in a timely and effective manner.
  • Team Player with ability to develop strong working relationships.
  • Demonstrated problem solving skills. Highly motivated individual, self-starter with a passion for excellence.
  • Must be able to work in a fast-paced environment.
  • Excellent attention to detail.
  • Knowledge of relevant ISO, EU, FDA medical devices standards regulations is required.
  • High self-motivation, self-starter with a passion for excellence.
  • Good working knowledge of Microsoft Office.
  • Willingness and availability to travel on company business.

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