Electrical Engineer III

Description: Electrical Engineer III Onsite pplicants must be authorized to work in the U.S. without visa sponsorship now or in the future. The Client is unable to consider candidates who require sponsorship. Job Purpose Develop and test new circuit blocks as part of manufacturing a medical device. Independently or as a member of a team directs, develops, conceives, and executes specifications, designs, plans, and builds of PCBA's as part of a medical device. Key Responsibilities 1. Leads or participates on project teams to develop clear specifications, evaluatesthe feasibility of concepts, and provides formal estimates for electrical designs. 2. Coordinates, monitors, and documents project designs, protocols, technical documents, and statistical analysis. 3. Creates electrical designs utilizing the department's standard development tools and procedures. 4. Translates hardware requirements into an executable test protocol and performs bench testing to confirm the product meets requirements. 5. Prepares standard reports/documentation to communicate status and results 6. Works with project teams that include Designers, Engineers, and Technicians in the design, assembly, and debugging of equipment. 7. Designs electrical systems and specifies electrical components. 8. Creates electrical engineering test set-ups and performs testing using oscilloscopes, power supplies, and multimeters. 9. Completes FDA/QSR equipment requirements by assisting in the creation of specifications and qualifications. 10. Provides training as required to ensure that the control systems can be operated effectively. 11. Influences and defines functional, departmental, and divisional procedures through involvement with cross-functional engineering initiatives. Quality Systems Duties and Responsibilities: Build Quality into all aspects of their work by maintaining compliance with all quality requirements. Qualifications 5 - 8 Years with BS, 3 - 6 Years with MS, 0 - 3 Years with PhD Electrical Engineering or Biomedical degrees only. ny work within the medical device industry. ny work in a highly regulated industry, such as automotive or aerospace. dditional Job Specific Requirements: ny experience with design verification testing (DVT) ny experience writing test protocols. ny experience with statistical analysis, preferably Minitab.

Created: 2026-03-10