# Senior System Verification Engineer, Software at Neko Health

Senior System Verification Engineer, Software at Neko Health in Stockholm. Hybrid, full-time. Posted September 1, 2026.

- Company: Neko Health
- Location: Stockholm
- Workplace: Hybrid
- Job type: Full-time
- Experience: 7+ years
- Posted: 2026-09-01
- Apply: https://jobs.ashbyhq.com/neko-health/f5504d99-38e5-4f36-b0d4-0c017d5e039c/application
- Source: https://jobmagic.ai/jobs/senior-system-verification-engineer-software-neko-health-pavmaw

## Requirements

- 7+ years verifying software, with at least 3–4 of those in a regulated industry, ideally recently. SaMD or health software is ideal, but automotive, aerospace or GxP experience also works if you can learn the medical standards quickly.
- Judgement from experience: you know which processes, tools and ways of working create confidence and which only create paperwork.
- You have integrated verification into development and release pipelines (CI/CD).
- You understand test automation well enough to direct, review and improve it.
- You're comfortable with code and repositories, and you use AI tools in your own work.
- You can create audit-ready V&V plans, traceability matrices and reports.

## Description

### **Mission**

Neko is redefining what prevention means, from treating illness when it arrives, to sustaining health before it's ever at risk. Our mission: make data-driven, preventative care accessible to more people, before symptoms appear.

In a single, non-invasive visit under an hour, proprietary technology and direct clinical care combine to deliver personalised, actionable insights. It's a team that thinks in 10x, not 10%. Every role here plays a part in building a world where prevention is the norm, and where your work genuinely helps people live longer, healthier lives.

### **About the role**

Our software informs clinical decisions, and we develop it with AI tools at the centre of the workflow. Traditional verification, with late manual test cycles and document-heavy handovers, can't keep up. You'll rethink how system-level verification of SaMD and health software works in this environment, and put it into daily use with Engineering, Quality and Regulatory. You'll join our growing, fast-moving Verification and Validation team.

### **What you'll do**

- Define how we verify health software at system level: what is tested, where, by whom, and with what evidence.

- Build verification into AI-driven development, not bolt it on afterwards.

- Evaluate and adopt tools and AI agents for test design, automation, impact assessment and evidence generation, based on what works.

- Decide where an automated check is enough and where human review is needed, and make sure wrong calls are caught and fed back.

- Turn requirements into test methods and acceptance criteria and push back when a requirement isn't testable.

- Make traceability and audit-ready evidence a by-product of the work, not a separate task.

- Keep us compliant with IEC 62304, ISO 14971, IEC 82304-1, ISO 13485, EU MDR and FDA 21 CFR Part 820, and help engineers find the fastest compliant route.

### **About you**

Must-have:

- 7+ years verifying software, with at least 3–4 of those in a regulated industry, ideally recently. SaMD or health software is ideal, but automotive, aerospace or GxP experience also works if you can learn the medical standards quickly.

- Judgement from experience: you know which processes, tools and ways of working create confidence and which only create paperwork.

- You have integrated verification into development and release pipelines (CI/CD).

- You understand test automation well enough to direct, review and improve it.

- You're comfortable with code and repositories, and you use AI tools in your own work.

- You can create audit-ready V&V plans, traceability matrices and reports.

Nice to have:

- Having built a test automation framework from scratch.

- Having designed a verification process or toolchain in a regulated setting.

- Verifying ML-based or algorithmic software.

- Verifying software across cloud and mobile.

- Experience with FDA submissions, EU MDR technical files or Notified Body audits.

- Experience with embedded verification, on products where software runs on specific hardware.

### Why this role matters

Our software portfolio is growing faster than manual verification can scale, and it carries clinical decisions: what a member is told about a mole, a blood pressure reading or a heart signal. As a Senior System Verification Engineer, Software you build the verification that makes those answers trustworthy, and the automation that keeps it fast enough to ship frequently/regularly.