Senior Electrical Test Engineer — Medical Device (Hybrid — Valencia, CA) Contract – Possible Contract to Hire

Pharmavise Corporation; Valencia; On-site; 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

Senior Electrical Test Engineer — Medical Device (Hybrid — Valencia, CA) Contract – Possible Contract to Hire

valencia, United States | Posted on 04/06/2026

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp

Job Description

Job Summary: Design custom automated test equipment (ATE) in support of R&D Verification/Validation and production test equipment for both new product development and existing product sustaining. This includes writing test requirements, test specs, test software, test procedures, validation plans and reports.

Responsibilities and Job Requirements:

• Design custom automated test equipment (ATE) including overall system design, electronic circuit design and test software programming.
• Leading the ATE process from early prototype stage working with design team to delivering a validated test equipment to manufacturing.
• Define and develop test requirement and test specifications for optimize test while working closely with the design, manufacturing and quality team.
• Perform test system statistical analysis, defining all required test equipment, estimating costs and determining test equipment build schedule.
• Generate related documents such as manufacturing test specifications, test software requirements, software intended use, test procedure, validation plan and report.
• Validate test systems and test fixtures in FDA-regulated medical environment.
• Support product troubleshooting for sustaining products.
• Support verification and validation testing of new product development.

Preferred requirements:

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

Specialized Knowdledge & Skills:

• Test system design for high reliability applications: Experience designing test systems for medical, aerospace, automotive, or other high reliability applications.
• Experience with electronic test system design/development.
• Experience with various types of data acquisition.
• Ability to document designs and reports in a clear and concise manner.
• Good interaction with other team members in the development of specifications and in the troubleshooting process.

Other Details:

Schedule: 08:00:AM - 04:30:PM

Contract Length: 12 months with Possible Extension ( 4/27/2026 - 4/27/2027 )

Work Set-Up:Hybridin Valencia, CA

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.