Senior Neurovascular Design Quality Engineer

Medtronic; Irvine (CA); On-site; USD 107,000 - 161,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid time off

Job summary

Medtronic is seeking a Neurovascular Senior Design Quality Engineer to influence design decisions, lead reliability studies, and apply risk management across the product lifecycle. You will partner with R&D and Process Development to ensure safe, effective neurovascular devices and drive design quality improvements.

Ideal candidates have 4+ years in engineering/quality, strong statistical skills, and familiarity with ISO 13485, EU MDR, and FDA QSR in a regulated medical-device setting. U.S.

Qualifications

• Bachelor's degree in engineering or science and 4+ years in engineering/quality.
• Experience supporting product development, design quality, or quality engineering.
• Experience with regulated environments, design control, risk management, verification or validation.

Responsibilities

• Lead reliability studies, design characterization activities, and DOE.
• Apply risk management to identify and mitigate risks from development through commercialization.
• Develop test methods, statistical approaches, and process controls to meet reliability objectives.
• Analyze product performance data and investigations to identify improvements.
• Provide quality leadership for verification, validation, and design transfer.

Skills

Statistical analysis

Risk management

Design quality

DOE

Process controls

Data analysis

Regulatory knowledge

Education

Bachelor's degree in Engineering or Science

Tools

Minitab

Job description

Medtronic is seeking a Neurovascular Senior Design Quality Engineer to influence design decisions, lead reliability studies, and apply risk management across the product lifecycle. You will partner with R&D and Process Development to ensure safe, effective neurovascular devices and drive design quality improvements.

Ideal candidates have 4+ years in engineering/quality, strong statistical skills, and familiarity with ISO 13485, EU MDR, and FDA QSR in a regulated medical-device setting. U.S.