Software Safety Engineer Ii

Medtronic Diabetes

Ireland
Base: 48,000.00 eur - 72,000.00 eur; bonus/equity:...
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Iso 14971 risk management experience
Software safety hazard analysis
Design verification traceability
** Medtronic Diabetes is seeking a Software Safety Engineer II in Ireland to identify and mitigate patient safety hazards in software, conduct risk analyses, and ensure compliance with regulatory standards. The role emphasizes collaboration with cross-functional teams and requires experience in safety engineering within a regulated environment. **

Job Summary

  • The role involves identifying, analyzing, and mitigating patient safety hazards in Medtronic software while collaborating with cross-functional teams.
  • Candidates must develop and maintain risk management files in strict compliance with ISO 13485, ISO 14971, and IEC 62304 standards.
  • Medtronic offers a competitive salary, flexible benefits package, and a commitment to supporting employees at every career stage.

Matching Summary

Match Score: 75

** Medtronic Diabetes is seeking a Software Safety Engineer II in Ireland to identify and mitigate patient safety hazards in software, conduct risk analyses, and ensure compliance with regulatory standards. The role emphasizes collaboration with cross-functional teams and requires experience in safety engineering within a regulated environment. **

Salary

Base: 48,000.00 EUR - 72,000.00 EUR; Bonus/Equity: Eligible for Medtronic Incentive Plan (MIP); Benefits: Flexible Benefits Package

Skills & Requirements

Must-have

  • ISO 14971 Risk Management experience
  • Software safety hazard analysis
  • Design verification traceability
  • Regulatory compliance ISO 13485
  • Reliability engineering studies

Nice-to-have

  • AI tools working knowledge
  • Agile methodologies proficiency
  • Innovation and team velocity focus
  • Statistical process control techniques

Key Requirements

  • Bachelor's degree in engineering or related field
  • Minimum 2 years of work experience in engineering or quality
  • Experience in highly regulated industry preferably implantable medical devices

Work Rights

Not specified

Tailored Resume

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