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 growth – the first product is just the beginning, and the software architecture is designed to support a wide range of diagnostic tests ahead.
Now we’re looking for a full-stack Software Engineer to join us permanently. You’ll get real ownership over our software in a small team where quality, traceability, and careful engineering aren’t just buzzwords – they’re how we work every day.
🔬 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/quality team and work alongside experienced external specialists we bring in for specific challenges.
Day to day, this means:
- Developing and shipping features across backend, web, and mobile applications
- Working within a regulated IEC 62304 software lifecycle – writing clear 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 to meet ISO 13485 and IVDR requirements
- 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
- 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:
- Experience in a regulated field (medical device, IVD, healthcare, pharma) – 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
- Real ownership: our software is continuously evolving, and you’ll have genuine influence over architecture, tooling, and ways of working
- Valuable MedTech specialization and experience of regulated software engineering
- 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 2 March 2026. Include your salary request and earliest possible start date.