Reliability Engineer II, Medical Devices (Post-Market)

Medtronic plc; Minneota (MN); On-site; USD 75,000 - 110,000; Full time

Job summary

Medtronic is seeking a Reliability Engineer II for its Mounds View, Minnesota facility. The role focuses on supporting post-market surveillance and quality activities for implantable cardiac rhythm management products, analyzing performance data, and documenting findings to improve device reliability and patient safety.

You will collaborate with cross-functional teams to investigate quality issues, conduct risk assessments, and support corrective actions while ensuring compliance with 21 CFR

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

Statistical data analysis

Reliability engineering

Cross-functional collaboration

Education

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

Job description

Medtronic is seeking a Reliability Engineer II for its Mounds View, Minnesota facility. The role focuses on supporting post-market surveillance and quality activities for implantable cardiac rhythm management products, analyzing performance data, and documenting findings to improve device reliability and patient safety.

You will collaborate with cross-functional teams to investigate quality issues, conduct risk assessments, and support corrective actions while ensuring compliance with 21 CFR