We’re building point-of-care IVD diagnostic software that helps clinicians make faster, better decisions for their patients. We’re ISO 13485 certified and approaching our first product certification. Our platform is built for scaling up – the first test is the beginning, and the software architecture is designed to work as a platform for a wide range of diagnostic tests ahead.
Now we’re looking for a full-stack Software Engineer to join us permanently. You’ll have real ownership of our software in a small team, where quality, traceability, and careful engineering are part of our daily workflow to ensure patient safety.
🔬 What you’ll do
You’ll work across our full stack – backend, frontend, and mobile – developing features, maintaining quality, and making sure our software meets the standards required for a regulated medical device. You’ll collaborate closely with our QARA team and work alongside experienced external specialists we bring in for specific technical challenges.
Day to day, this means:
- Developing and shipping high-quality features across backend, frontend, and mobile applications
- Working within a regulated IEC 62304 software lifecycle – writing clear software requirements, keeping documentation up to date, and maintaining traceability
- Developing and maintaining test automation, CI/CD pipelines, and release processes
- Contributing to cybersecurity practices, including secure development, vulnerability monitoring, and compliance with IEC 81001-5-1
- Collaborating with quality and regulatory colleagues on verification and validation (V&V) activities
- Maintaining monitoring and observability for production systems
Our stack: C#, .NET, Azure, React, TypeScript, React Native (iOS & Android), Jest, xUnit, App Insights, Azure DevOps, Azure B2C (Entra ID), Git
🔎 What we’re looking for
- 2-5 years of experience in full-stack software development
- Experience of software development or other product development activities in a regulated field (medical device, IVD, pharma)
- Comfort working across backend, frontend, and mobile
- Experience with CI/CD pipelines and automated testing
- Understanding of security, cloud infrastructure, and observability
- Strong written and spoken English
- Curiosity, a quality-first mindset, and a proactive approach to problem-solving
Strong advantages:
- Mindset suitable for a regulated field – you understand why documentation and traceability matter
- Familiarity with medical device standards (IEC 62304, IEC 81001-5-1, ISO 13485, IVDR)
- Finnish language skills
You don’t need to tick every box – curiosity and the right mindset matter more than a perfect CV.
💼 What we offer
- 4000–5500 EUR/month depending on experience
- Permanent, full-time position on-site in Espoo, Finland
- Real ownership: our software is continuously evolving, and you’ll have genuine influence over architecture, tooling, and ways of working
- A compact core team supported by experienced external specialists for specific domains (infrastructure, ML, and more) – you’re not on your own
- Hybrid work with flexible hours. Our Espoo team at Innopoli, Otaniemi enjoys working on-site most days (and the daily 14:00 coffee break), while collaborating seamlessly with Turku-based colleagues
- Edenred lunch and sports benefits
📩 How to apply
Send your CV and a short cover letter to careers@fepod.com by 6 April 2026. Please include your salary request and earliest possible start date. We review applications continuously and will hire as soon as we find the right match!
Please note that candidates must already have the right to work in the EU and be able to work on-site in Espoo. Unfortunately, we cannot provide relocation support or work visa sponsorship.