Medical Electronics Design Engineer: PCB & Components

Sii Sweden; Stockholms kommun; On-site; SEK 650,000 - 850,000; Full time

Job summary

Sii Sweden seeks an Electronics Design Engineer to develop a modular system for medical device interfaces, focusing on replacing components on existing PCBs and qualifying new parts to meet safety and regulatory standards. You will evaluate, test, analyze, and modify designs within defined timelines while documenting all work.

The role involves hands-on design, collaboration with cross-functional teams, and ensuring compliance with medical device requirements throughout the lifecycle of the

Qualifications

• 5+ years in electronic circuit and PCB design.
• Proficiency with schematic capture and hardware CAD tools (Altium, Xpedition).
• Strong understanding of embedded hardware architectures, microcontrollers, memory interfaces and peripherals.

Responsibilities

• Performing electronic design changes and component replacements on existing PCBs.
• Creating and updating schematics and selecting suitable components.
• Ensuring compliance with medical device requirements and safety standards.
• Conducting tests, measurements, and validation of new components.
• Supporting EMC activities and ensuring adherence to relevant regulations.
• Participating in hardware risk analysis and documentation work.
• Maintaining accurate technical documentation throughout the design lifecycle.
• Collaborate with cross-functional engineering teams.

Skills

PCB design

Schematic capture

Embedded hardware

EMC testing

Regulatory standards

Documentation

Cross-functional teams

Tools

Altium

Xpedition

Job description

Sii Sweden seeks an Electronics Design Engineer to develop a modular system for medical device interfaces, focusing on replacing components on existing PCBs and qualifying new parts to meet safety and regulatory standards. You will evaluate, test, analyze, and modify designs within defined timelines while documenting all work.

The role involves hands-on design, collaboration with cross-functional teams, and ensuring compliance with medical device requirements throughout the lifecycle of the