Electrical Engineer

Work Authorization: Must be authorized to work in the U.S. (no sponsorship available)

(1 Year contract with opportunity for perm)

We’re seeking an experienced Electrical Engineer III to support the development and testing of advanced electronic systems used in highly regulated medical technology. In this role, you’ll design, build, and validate PCBAs and electrical subsystems, working both independently and as part of a collaborative engineering team. You’ll contribute to concept development, feasibility evaluation, test protocol creation, and hands‑on bench testing to ensure products meet stringent performance and regulatory requirements.

• Lead or participate in project teams to define specifications, assess feasibility, and provide accurate estimates for electrical design work.
• Develop electrical designs using established engineering tools, standards, and procedures.
• Translate hardware requirements into executable test protocols and perform bench testing to confirm compliance with design requirements.
• Design electrical systems and specify appropriate components for new or existing products.

• Create electrical engineering test setups and perform testing using oscilloscopes, power supplies, multimeters, and other lab equipment.
• Prepare clear, standardized reports and documentation to communicate project status, test results, and design decisions.
• Support design verification testing (DVT), including protocol development and execution.
• Assist in meeting regulatory and quality system requirements, including FDA/QSR equipment specifications and qualifications.

• Coordinate, monitor, and document project designs, protocols, technical documents, and statistical analyses.
• Work closely with designers, engineers, and technicians during design, assembly, and debugging activities.
• Provide training and guidance to ensure electrical and control systems are properly understood and operated.
• Influence and help define departmental and cross‑functional engineering procedures.

• Integrate quality into all aspects of work by maintaining full compliance with applicable quality system requirements and documentation standards.

• BS in Electrical Engineering or Biomedical Engineering: 5–8 years
• MS: 3–6 years
• PhD: 0–3 years

• Experience in medical device development or other highly regulated industries (e.g., aerospace, automotive).
• Strong understanding of test method development, documentation, and training.
• Experience writing test protocols and performing design verification testing.
• Familiarity with statistical analysis tools (preferably Minitab).

• Hands‑on experience with PCBA development, electrical debugging, and bench‑level testing.
• Background in regulated product development environments with exposure to quality systems and compliance requirements.