Jobs / Ireland / Medtronic INC

Medtronic INC

Principal Mechanical Design Engineer

Galway, County Galway, Ireland Posted today

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Sponsorship verdict

No sponsorship evidence yet

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  • No government sponsor record hereNo government sponsor record covers this employer in this country.
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  • 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).
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Can’t check pay against the visa rules
No 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.

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Before you apply

Sponsorship unknown

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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 The Principal Mechanical Engineer in Electrophysiology Technologies (EPT) serves as a recognized technical authority responsible for the architecture, design, verification, and lifecycle support of complex electromechanical systems used in cardiac mapping and ablation therapies. The role provides technical leadership across released product engineering and technology innovation, with a strong focus on patient safety, product reliability, regulatory compliance, risk management, and sustainable product performance. Operating with a high degree of autonomy and ownership, the Principal Engineer identifies and drives technical priorities, provides direction across multiple programs, mentors engineers, and influences cross-functional decisions involving systems, firmware, electrical, mechanical, manufacturing, quality, regulatory, and supplier teams. The role is expected to anticipate risks, resolve ambiguity, make sound engineering decisions, and drive complex issues through implementation and closure.   Primary Responsibilities:  • Own and drive mechanical engineering activities for released products, from problem definition and technical assessment through design implementation, verification, release, and post-implementation monitoring. • Develop and implement mechanical design improvements that enhance patient safety, product performance, system reliability, serviceability, and scalable manufacturing. • Provide technical leadership for complex, ambiguous, or high-risk product and process issues; establish investigation strategies, make evidence-based decisions, and ensure actions are driven to effective closure. • Lead cross-functional technical teams in investigating product and process issues, applying structured root-cause analysis to define, implement, and verify effective corrective and preventive actions. • Apply sound engineering fundamentals, analytical methods, tolerance analysis, material selection, and design verification techniques to support robust mechanical solutions. • Create and review 3D models, engineering drawings, specifications, technical reports, and presentations; ensure design outputs are complete, accurate, and suitable for release. • Design, qualify, document, and maintain test fixtures, jigs, and tools, and provide technical oversight for associated testing activities. • Lead or support test method development and validation, design verification and validation, and the interpretation and communication of results. • Integrate risk-based decision-making and Design for Reliability and Manufacturability principles throughout design and development activities. • Own timely, high-quality completion of applicable design control deliverables, technical reviews, product configuration activities, and engineering changes. • Collaborate with program management, Manufacturing, Quality, Regulatory, Systems, Electrical, Firmware, and external suppliers on component selection, manufacturing processes, assembly methods, and product improvements. • Investigate audit findings, process flows, and systemic gaps, and translate findings into practical, sustainable engineering improvements. • Partner with Quality as a primary technical point of contact during internal and external audits and provide clear, evidence-based responses. • Prese

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