Jobs / Ireland / Medtronic INC

Quality Engineer I

Medtronic INC · 🌍 Galway, County Galway, Ireland

Sponsorship verdict

No sponsorship evidence yet

No government record and no wording either way. Not a refusal — ask the recruiter.

  • No government sponsor record hereNo government sponsor record covers this employer in this country.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • Can’t check pay against the visa rulesNo salary stated. Ireland Critical Skills Employment Permit needs at least €40,904 a year (General Employment Permit: €36,605). Source: https://enterprise.gov.ie/en/what-we-do/workplace-and-skills/employment-permits/permit-types/critical-skills-employment-permit/, rules effective 2026-03-01.
  • Confirmed live todayWhen a source last listed this job as open.

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Sponsor Radar — Medtronic INC

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About the role

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life At our Quality Department in Medtronic, plc, we focus on supporting the product value stream to ensure that customer and patient needs are met every day. Our key focus is on delivering and maintaining a high level of Quality to ensure that business and performance goals are achieved. The Quality Engineer role is critical in supporting key department metrics thus contributing to the global strategy and to deliver on our mission to contribute to human welfare by supporting the manufacture of products that alleviate pain, restore health, and extend life. Responsibilities may include the following and other duties may be assigned: • Supports the development, modification, application and maintenance of quality standards and procedures for manufacturing processes and finished products. • Works collaboratively with Engineering, Manufacturing and Quality teams to ensure compliance with quality system requirements. • Collaborate with required stakeholders in the receive inspection function and across functions ensuring incoming materials and components meet defined specifications and regulatory requirements. • Assists in implementing and maintaining product control measures to ensure product quality and patient safety. • Reviews quality data, identifies trends and supports problem-solving activities to address quality issues. • Supports inspection and testing activities and assists in the analysis of product and process performance. • Applies and implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of raw materials and test equipment • Ensure quality records and documentation are completed accurately and maintained in compliance with applicable regulatory and internal requirements. • Participate in preparing and facilitating investigations, providing QA technical direction and solutions as appropriate. • Contributes to continuous improvement initiatives to enhance product quality, process effectiveness and operational performance. • Supporting internal and external audits (BSI/MDSAP/FDA etc.).     Key Skills & Experience • Level 8 Bachelor’s degree in Engineering, Science or technical field • Demonstrated analytical and problem-solving skills with the ability to apply a risk-based approach to quality issues. • A dynamic team player and leader with the ability to work effectively and proactively on cross-functional teams with a high level of enthusiasm and motivation while developing technical and quality engineering knowledge. • Strong communication, organisational and interpersonal skills. • Ability to manage multiple priorities and deliver work within established timelines. • Demonstrated critical thinking skills and ability to independently plan and schedule activities. • Experience or knowledge of quality systems, equipment IQ/OQ/PQ, validation activities or regulated industries is advantageous. • Experience with Agile, SAP and/or SAP ME would be beneficial. • Fluent in English, both written and verbal.   Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.  ‌ ‌     Recruitment

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Source: Employer career site (Workday) First seen: 2026-10-02 Last confirmed: 2026-10-02 How our data works → Report this job

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