Medtronic
Healthcare
QualityEngineer-NightShift
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Engineer - Night Shift at Medtronic. Skills: Quality assurance, Process improvement. Develop quality standards. Modify quality standards”
Industry & Context.
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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