Lead Design Assurance Engineer – Medical Devices (Hybrid)

Medtronic plc

Galway

Hybrid

EUR 90.000 - 130.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Benefits dieser Stelle

Competitive salary
Benefits package
Hybrid work

Zusammenfassung

Medtronic plc in Galway is seeking a Principal Engineer to lead risk management, reliability, design verification and shelf-life protocols. You will mentor junior engineers and ensure regulatory compliance across FDA, ISO standards.

This hybrid role requires four onsite days per week and close collaboration with multiple teams. The successful candidate will hold an NFQ Level 8 Engineering degree (7+ years of relevant experience) or an advanced degree with 5+ years, with DRM certification

Qualifikationen

  • Requires an advanced engineering degree with 7+ years of related experience.
  • NFQ Level 8 in Engineering or related discipline; advanced degree acceptable.
  • DRM certification is advantageous.

Aufgaben

  • Lead risk management, reliability, design verification and shelf-life workstreams.
  • Mentor junior engineers on the project and within the department.
  • Maintain up-to-date knowledge of regulatory requirements (FDA, ISO 14971/13485).
  • Collaborate with internal and external stakeholders to build partnerships.
  • Provide technical guidance on component qualification (PPAP).
  • Ensure design quality activities align with project goals.
  • Support cross-functional teams across design and development.

Kenntnisse

Regulatory knowledge
Project management
Cross-functional collaboration
Communication skills

Ausbildung

NFQ Level 8 Engineering degree
Advanced degree (optional)

Tools

Design for Six Sigma (DRM)

Jobbeschreibung

Medtronic plc in Galway is seeking a Principal Engineer to lead risk management, reliability, design verification and shelf-life protocols. You will mentor junior engineers and ensure regulatory compliance across FDA, ISO standards.

This hybrid role requires four onsite days per week and close collaboration with multiple teams. The successful candidate will hold an NFQ Level 8 Engineering degree (7+ years of relevant experience) or an advanced degree with 5+ years, with DRM certification

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