Reliability Engineer II

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

Reliability Engineer II at Medtronic's Mounds View, Minnesota facility will support post-market surveillance and quality activities for implantable cardiac rhythm management products. The role involves analyzing product performance data, conducting risk assessments, investigating quality issues, and documenting technical findings to improve device reliability and patient safety.

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

Requirements

• 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