100% ONSITE Pleasanton, CA
Pay: $75-$82/hr
REQUIRED:
Prefer
Job Description:
The Electrical Test Engineer will be responsible for performing and documenting verification and integration activities of complex electro-mechanical medical devices with software. It includes testing of specified components and overall product functionality to ensure product safety and efficacy. The engineer is experienced in all aspects of product development life cycle with understanding of systems engineering processes in Medical Device industry. The Electrical Test Engineer will work with a multi-disciplinary engineering teams including system, software, electrical, and mechanical design engineers, and other functions to ensure the highest quality for class II medical devices.
Main Areas of Responsibilities:
• Perform the Electronics Design and EMC pre-test activities for complex electro-mechanical medical device products within the Product Development team
• Identify electrical tests, prepare electrical test environment and ensure test preconditions are met prior to formal testing activities
• Verify (including TEC / low voltage power control / AC voltage and current / PCB / FPGA / analog electrical components tests) that Analog and Digital electrical design that electrical system, sub-systems and appropriate supporting documentation meet detailed design as well as related requirement specifications, while ensuring that related standards are applied
• Verify (including EMC / EMI / ESD / Radio tests) that system with related electrical design and appropriate supporting documentation meets all safety, regulatory and industry compliance standards, and codes while ensuring that related standards are applied
• Help build Electrical Test Lab, and support testing of Electronics Design and EMC Testing in the Test Lab; follow Laboratory Best Practices and safety protocols
• Develop and maintain verification protocols, verification reports, requirements documents, and other related technical documentation while ensuring related international standards are applied
• Verify translation of Design Inputs into test design and test protocols, and support creation of system architecture and detailed design documentation
• Contribute to risk analysis activities for the product development including hazards analysis, Design FMEA, and Use FMEA
• Safely work with hazardous systems containing high / low voltage, high / low temperatures, high acoustic, and high pressure
• Support review and approval of design and process changes as well as deviations related to new and existing medical device products
• Communicate and collaborate with a wide range of project contributors and stakeholders spanning the organization, and external partners including technical leaders for product design, development, integration, testing, and reliability improvements
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