Senior Medical Device ATE Engineer — LabVIEW

Pharmavise Corporation; California (MO); Hybrid; USD 110,000 - 150,000; Full time

Job summary

Pharmavise Corporation in Valencia, CA is seeking a Senior Electrical Test Engineer to design custom automated test equipment (ATE) for R&D verification and production testing. The role spans from prototype through manufacturing, with a focus on high-reliability medical device testing in a hybrid work setting.

You will define test requirements, develop tests and documentation, analyze test data, and support troubleshooting and V&V for new product development within an FDA-regulated environment.

Qualifications

• BS degree in Electrical Engineering required; MS preferred.
• 5+ years electronics and software design experience.
• 2+ years experience with LabVIEW programming preferred.

Responsibilities

• Design ATE including system and circuit design and test software.
• Lead ATE from prototype to validated manufacturing equipment.
• Define test requirements and specs with design, manufacturing and quality teams.
• Perform test system statistics, cost estimates and build scheduling.
• Create documents: test specs, software requirements, procedures and reports.
• Validate test systems in FDA-regulated medical environment.
• Support troubleshooting for sustaining products.
• Support verification and validation testing for new product development.

Skills

Electronics design

Software design

Test system design

Education

Bachelor's degree in Electrical Engineering

Master's degree preferred

Tools

LabVIEW

Job description

Pharmavise Corporation in Valencia, CA is seeking a Senior Electrical Test Engineer to design custom automated test equipment (ATE) for R&D verification and production testing. The role spans from prototype through manufacturing, with a focus on high-reliability medical device testing in a hybrid work setting.

You will define test requirements, develop tests and documentation, analyze test data, and support troubleshooting and V&V for new product development within an FDA-regulated environment.