Staff Electrical Engineer – PCB (Medical Devices, Hybrid)

Stryker; Portage (MI); Hybrid; USD 89,000 - 149,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Stryker Corporation in Portage, Michigan, is seeking a Staff Electrical Engineer-PCB to advance existing medical device products. You will design electrical components, lead prototyping and testing, and translate clinical needs into robust specifications for safe, reliable operation.

You will collaborate with R&D, Quality, Manufacturing and Regulatory teams, maintain DHF documentation and mentor juniors while applying design controls and industry standards in a hybrid onsite work environment.

Qualifications

• Bachelor’s degree in Electrical Engineering or related field.
• 4+ years of relevant engineering experience.
• PCB/circuit design, electrical system testing and troubleshooting experience.
• Ability to interpret and analyze system-level drawings and interactions.

Responsibilities

• Design and develop electrical components and subsystems for medical devices, meeting performance and compliance standards.
• Apply advanced circuit and system test methods to validate designs and ensure reliability.
• Lead prototyping and testing efforts to evaluate design feasibility and performance.
• Translate user needs into design inputs and specifications, ensuring alignment with clinical requirements.
• Collaborate across R&D, Quality, Manufacturing and Regulatory teams to drive project success.
• Author and maintain engineering documentation, including Design History Files, in compliance with regulatory standards.
• Mentor team members on design controls, risk management, and industry standards.

Skills

PCB design

Electrical testing

Troubleshooting

System analysis

Education

Bachelor’s degree in Electrical Engineering

Job description

Stryker Corporation in Portage, Michigan, is seeking a Staff Electrical Engineer-PCB to advance existing medical device products. You will design electrical components, lead prototyping and testing, and translate clinical needs into robust specifications for safe, reliable operation.

You will collaborate with R&D, Quality, Manufacturing and Regulatory teams, maintain DHF documentation and mentor juniors while applying design controls and industry standards in a hybrid onsite work environment.