Medtronic

Healthcare

QualityEngineer-NightShift

€42–62k Galway, County Galway, Ireland FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Quality Engineer - Night Shift at Medtronic. Skills: Quality assurance, Process improvement. Develop quality standards. Modify quality standards”

Industry & Context.

Healthcare
Problems you'll solve

Problem solving

What They're Looking For.

Must Have

Bachelor's degree in Engineering/Science, 1-year relevant experience, Experience in medical device environment

Nice to Have

Working knowledge of statistical data analysis, Working knowledge of problem solving tools, Working knowledge of quality improvement tools

What You'll Do.

Develop quality standards

Modify quality standards

Apply quality standards

Maintain quality standards

Collaborate with engineering

Collaborate with manufacturing

Ensure quality standards

Devise inspection methods

Implement inspection methods

Devise testing methods

Implement testing methods

Devise evaluation methods

Implement evaluation methods

Work on non-conformance investigations

Ensure corrective measures meet reliability

Ensure documentation compliance

Contribute to continuous improvement

Collaborate in design

Collaborate in incoming material

Collaborate in production control

Collaborate in product evaluation

Collaborate in reliability

Collaborate in inventory control

Collaborate in research and development

Ensure compliance with procedures

Ensure compliance with regulations

Support audit preparation

Support audit activity

Maintain quality standards

How You'll Work.

Team & Collaboration

Engineering functions; Manufacturing functions

Communication Scope

Interpersonal skills

Full Job Description

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. # **A Day in the Life** **A Day in The Life Of:** Responsibilities may include the following and other duties may be assigned: * Develops, modifies, applies and maintains quality standards and protocols for processing materials into partially finished or finished materials product. * Collaborates with engineering and manufacturing functions to ensure quality standards are in place * Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment * Work on non-conformance Investigations * Ensures that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements * Contribute to continuous improvement activities to support the business * May collaborate in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality * Ensure compliance with all applicable departments and site-wide procedures, and regulations. Support Internal and External audit preparation and activity which includes application and maintenance of quality standards for all activities associated **Key Skills & Experience ** * Minimum of a bachelor’s degree (Level 7 NFQ) in Engineering/Science or related discipline with a minimum of 1-year relevant direct Science/Engineering experience within medical device environment * Strong interpersonal, communication and organizational skills * Practical working knowledge of statistical data analysis, problem solving and quality improvement tools and techniques preferable * Technical writing skills * Ability to multi-task and to take initiative is essential * Effect

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