Senior Staff Engineer, Medical Device Test & Automation

Stryker; San Jose (CA); On-site; USD 133,000 - 222,000; Full time

Job summary

Stryker in the United States is seeking an experienced Test Engineer to design and implement ICT, functional, and electromechanical test processes for medical device products across development and manufacturing stages.

You will drive equipment qualification, process validation, and statistical analysis (Gauge R&R, DOE) to ensure robust production readiness, while partnering with design and manufacturing teams to improve testability and manufacturability.

Qualifications

• Bachelor's degree in EE or a related field.
• 8+ years of progressive engineering experience with a bachelor’s degree, or 6+ years with a master’s.
• Experience developing and implementing PCBA manufacturing test strategies.
• Experience with LabVIEW and TestStand environments.
• Knowledge of process risk analysis, control plans, and equipment qualification methodologies.
• Experience applying Gauge R&R and process capability analysis.

Responsibilities

• Design and implement ICT, functional and electromechanical test processes for new and existing products across development and manufacturing.
• Execute process verification, equipment qualification, and validation activities, including Gauge R&R, DOE, and SPC.
• Develop test fixtures, schematics, instrumentation, and test documentation to improve test coverage and quality.
• Troubleshoot complex manufacturing and test issues with production teams, suppliers, and contract manufacturers to identify root causes and corrective actions.
• Partner with design and manufacturing engineering teams to provide design-for-testability and design-for-manufacturing recommendations during NPI and process transfer.

Skills

LabVIEW

TestStand

PCBA testing

Gauge R&R

Education

B.S. in EE

Tools

LabVIEW

TestStand

Job description

Stryker in the United States is seeking an experienced Test Engineer to design and implement ICT, functional, and electromechanical test processes for medical device products across development and manufacturing stages.

You will drive equipment qualification, process validation, and statistical analysis (Gauge R&R, DOE) to ensure robust production readiness, while partnering with design and manufacturing teams to improve testability and manufacturability.