Reliability Engineer II - Cardiac Devices, Post‑Market

Medtronic plc; Saint Paul (MN); On-site; USD 85,000 - 110,000; Full time

Job summary

Medtronic plc is seeking a Reliability Engineer II at its Minnesota facility to support post-market surveillance and quality activities for implantable cardiac rhythm management products. You will analyze performance data, perform risk assessments, investigate quality issues, and document findings to improve device reliability and patient safety.

The role requires collaboration with cross-functional teams, verification and validation activities, and compliance with medical device standards.

Qualifications

• Bachelor's degree in Engineering, Science, or related technical discipline.
• Minimum 2 years work experience in Engineering or related technical field.
• Understanding of cardiac rhythm management products and clinical environments.
• Experience with medical device regulations (21 CFR 820, ISO 13485, ISO 14971).
• Root cause investigation and risk assessment capabilities.
• Statistical data analysis and reliability engineering tools proficiency.
• Unrestricted U.S. work authorization required.

Responsibilities

• Support reliability analysis to identify design and process improvements for device systems.
• Conduct or assist with risk assessments and technical documentation for quality and safety impact.
• Analyze post-market product performance data and summarize findings for surveillance activities.
• Collaborate with cross-functional teams to investigate quality issues and support corrective actions.
• Support verification, validation, and compliance assessment of device requirements and standards.

Skills

Root cause analysis

Risk assessment

Statistical data analysis

Reliability engineering

Education

Bachelor's degree in Engineering, Science, or related discipline

Job description

Medtronic plc is seeking a Reliability Engineer II at its Minnesota facility to support post-market surveillance and quality activities for implantable cardiac rhythm management products. You will analyze performance data, perform risk assessments, investigate quality issues, and document findings to improve device reliability and patient safety.

The role requires collaboration with cross-functional teams, verification and validation activities, and compliance with medical device standards.