Manufacturing Engineer 2

3 weeks ago

Limerick, Limerick, Ireland Cook Ireland Ltd Full time
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.
To be considered for this role you will be redirected to and must complete the application process on our careers page.
To start the process click the Continue to Application or Login/Register to apply button below.

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