Reliability Engineer II, Post-Market Medical Devices

Medtronic; Minnesota; Hybrid; USD 85,000 - 127,000; Full time

Benefits offered by this job

Health, Dental and Vision Insurance

401(k) with employer match

Employee Stock Purchase Plan

Job summary

Medtronic is seeking a Reliability Engineer II at our Mounds View, MN facility. The role supports post‑market surveillance, risk assessments, technical documentation, and defect investigations for implantable devices.

Hybrid work requires on‑site collaboration most days and cross‑functional teamwork with EPT DS Post Market Quality. Responsibilities include analyzing data, validating designs, preparing technical reports, and supporting corrective actions to improve product reliability and patient

Qualifications

• Bachelor’s degree in Engineering, Science, or a technical discipline required.
• 2+ years in engineering/science or advanced degree in a technical field substitute.
• Experience with reliability engineering or risk management preferred.

Responsibilities

• Analyze, debug, and recommend design or process improvements for reliability.
• Support risk analyses to assess quality or patient safety risks.
• Prepare risk assessments, technical reports and documentation.
• Verify and validate device system requirements and traceability.
• Evaluate finished product systems across design, development, and testing.
• Interpret system requirements and ensure standards compliance.
• Collaborate with cross-functional teams to investigate quality issues and drive corrective actions.
• Analyze product performance data to support post-market surveillance and improvements.

Skills

Reliability engineering

Risk management

Data analysis

Cross-functional collaboration

Education

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

Advanced degree in Electrical Engineering, Engineering, Science, or related (for related path)

Tools

Statistical tools

Reliability tools

Job description

Medtronic is seeking a Reliability Engineer II at our Mounds View, MN facility. The role supports post‑market surveillance, risk assessments, technical documentation, and defect investigations for implantable devices.

Hybrid work requires on‑site collaboration most days and cross‑functional teamwork with EPT DS Post Market Quality. Responsibilities include analyzing data, validating designs, preparing technical reports, and supporting corrective actions to improve product reliability and patient