Senior Electrical Engineer - Medical Devices & Systems

BioSpace; North Chicago (IL); On-site; USD 140,000 - 190,000; Full time

Benefits offered by this job

Paid time off

Vacation

Holidays

Sick leave

Medical insurance

Dental insurance

Vision insurance

401(k)

Short-term incentive programs

Job summary

BioSpace is seeking a senior Electrical Systems Lead to drive the design of on-body injectors and infusion pumps. You will own system architecture, circuit and PCB design, and embedded software interfaces, ensuring robustness and safety across the development lifecycle.

Collaborating with external partners and cross-functional teams, you will navigate regulatory requirements such as ISO 13485 and contribute to risk assessments, design verifications, and validations for medical devices.

Qualifications

• Requires a BS in Electrical Engineering with 10+ years of experience or an MS with 8+ years.
• Experience in medical devices or combination products is required.
• Expertise in circuit and PCB design, embedded systems, and ISO 13485.

Responsibilities

• Lead electrical system design for advanced drug delivery systems.
• Collaborate with external partners and cross-functional teams to ensure robustness.
• Ensure regulatory compliance throughout the product development lifecycle.

Skills

Electrical system design

Circuit design

PCB design

Embedded systems

Medical device development

Design verification

Design validation

Risk assessment

System architecture evaluation

Project management

Regulatory compliance

Technical leadership

Analytical modeling

Simulation software

Cross-functional collaboration

Design history file documentation

Education

BS in Electrical Engineering, 10+ years experience

MS in Electrical Engineering, 8+ years

Job description

BioSpace is seeking a senior Electrical Systems Lead to drive the design of on-body injectors and infusion pumps. You will own system architecture, circuit and PCB design, and embedded software interfaces, ensuring robustness and safety across the development lifecycle.

Collaborating with external partners and cross-functional teams, you will navigate regulatory requirements such as ISO 13485 and contribute to risk assessments, design verifications, and validations for medical devices.