Embedded Software Developer – MedTech

Nexer Group; Göteborgs kommun; On-site; SEK 446,400 - 781,200; Full time

Job summary

Nexer Group is seeking Embedded Software Developers in Göteborg, Sweden. Your main focus will be on developing embedded software for safety-critical medical devices, ensuring compliance with medical device standards.

You will engage in all phases of the software development lifecycle, collaborate with multidisciplinary teams, and contribute to risk management and product quality.

The role offers opportunities for growth in a field impacting health and quality of life.

Qualifications

• Proven experience in embedded software development.
• Experience from regulated industries like MedTech or Life Science is a plus.
• Strong programming skills in Embedded C are essential.

Responsibilities

• Developing and maintaining embedded software for medical devices.
• Participating in software architecture and technical design activities.
• Working with software verification, validation, and unit testing.
• Supporting regulatory compliance and software documentation.

Skills

Embedded Software Development

Embedded C

Software Verification and Validation

Risk Management

Collaboration in Multidisciplinary Teams

Job description

Do you want to develop embedded software for medical devices that improve and save lives?

Nexer Engineering is looking for Embedded Software Developers for assignments within the MedTech industry in Sweden.

The focus is on embedded software development in regulated environments, with strong emphasis on product quality, patient safety, risk management, and compliance with medical device standards.

Your role

You will work throughout the embedded software development lifecycle, contributing to the development of safety‑critical medical devices and systems.

Responsibilities include:

• Developing and maintaining embedded software for medical devices
• Participating in software architecture and technical design activities
• Working with software verification, validation, and unit testing
• Contributing to risk management activities throughout the development process
• Supporting regulatory compliance and software documentation activities
• Collaborating closely with system engineers, quality teams, and cross‑functional development teams
• Ensuring compliance with applicable medical device standards and development processes

Your profile

• Proven experience in embedded software development
• Experience from the MedTech, Medical Device, Life Science, or other highly regulated industries
• Strong programming skills in Embedded C
• Experience developing software for embedded systems at a deep, low‑level hardware layer – hands‑on experience working close to the hardware is essential, not solely at the application level.
• Understanding of software development in safety‑critical or regulated environments
• Experience with software verification, validation, and testing activities
• Experience working throughout the complete software development lifecycle
• Ability to work in multidisciplinary product development teams

Nice to have

• Experience working according to IEC 62304
• Knowledge of medical device development processes and regulatory requirements
• Experience with risk management activities in product development
• Experience working with quality management systems in regulated environments
• Experience supporting audits, certifications, or regulatory submissions
• Swedish language skills
• Experience working within Swedish MedTech organizations

Why Nexer Engineering?

At Nexer Engineering, you will have the opportunity to work with innovative MedTech companies and contribute to products that have a direct impact on people's health and quality of life.

We offer long‑term assignments, strong technical communities, and opportunities to develop your expertise within embedded software, safety‑critical systems, and regulated product development.

Apply

If you have experience in embedded software development and MedTech environments, and want to work with advanced products in a highly regulated industry, we would like to hear from you.