Electronics Design Engineer – MedTech

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

Join Sii Sweden as an Electronics Design Engineer and contribute to the development of a cutting-edge medical device platform used in critical care. You will work within a cross-functional R&D team responsible for a modular system enabling the development, design, and production of user interface screens for medical devices.

In this project, you will focus on replacing electronic components on existing PCBs, qualifying new components, and ensuring that they meet safety, quality, and regulatory requirements. The work includes evaluation, testing, analysis, documentation, and design modification within defined timelines.

This role is ideal for a proactive and structured engineer who thrives in a regulated environment, enjoys hands-on design and problem-solving, and wants to make a real impact on products that support patient care worldwide.

Sii ensures that all employment-related decisions are made solely on the basis of qualifications and competencies. We are committed to equal treatment of all individuals, regardless of any protected characteristics, and promoting a diverse and inclusive work environment.

• 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

Requirements

• At least 5 years of experience in electronic circuit and PCB design
• Proficiency with schematic capture and hardware CAD tools (as Altium, Xpedition)
• Strong understanding of embedded hardware architectures, microcontrollers, memory interfaces, and peripheral components
• Experience with testing, debugging, and validating electronic hardware
• Knowledge of medical device standards, regulatory requirements, and safety-critical design principles is a huge plus
• Ability to interpret datasheets, design specifications, and electrical constraints