Neko Health operates AI-supported 10-minute full-body scanning clinics with in-person physician consultations to detect skin, cardiovascular, metabolic and diabetic conditions, and conducts R&D and clinical studies across Europe.
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. Neko Health is a Swedish healthcare technology company co-founded in 2018 by Hjalmar Nilsonne and Daniel Ek. Neko's vision is to shift healthcare from reactive treatment toward preventative health and early detection. This requires completely reimagining the patient's experience and incorporating the latest advances in sensors and AI. Neko Health has developed a new medical scanning technology concept to make it possible to do broad and non-invasive health data collection that is convenient and affordable for the public. The company is based in Stockholm, offering the Neko Body Scan experience at locations in Stockholm, London and Manchester, with over 500 employees. We are currently seeking a Senior System Verification Engineer to join our multidisciplinary engineering team. In this role, you will take ownership of system-level verification activities across the product lifecycle, from early concept through industrialization and market release. You will work closely with hardware, firmware, and software teams to ensure our medical device systems meet applicable standards and regulatory requirements, translating compliance needs into practical, testable requirements and robust verification strategies that ensure safety, performance, and regulatory compliance. Responsibilities - Partner with design engineers throughout the product development lifecycle to ensure medical device systems are compliant with applicable standards (e.g., IEC 60601 series) and regulatory requirements (e.g., FDA, MDR) from concept through industrialization - Translate regulatory requirements and standards into actionable, practical guidance for design decisions, serving as a bridge between regulatory/compliance and engineering teams - Influence product requirements early by working with cross-functional teams to ensure requirements are testable, traceable, and specify compliance needs effectively - Develop efficient verification methodologies, tools, and workflows, for end-to-end, integration, and regression testing, implementing automation where it optimizes work and increases reliability - Coordinate with external test houses for specialized testing (e.g., EMC, electrical safety, environmental.) and manage the interface between internal requirements and external verification activities - Ensure continuity of test requirements through design transfer, maintaining product quality, safety, and compliance as products move from development to manufacturing and industrialization - Create comprehensive test reports documenting results, defects, and compliance status, and communicate findings to stakeholders - Contribute to the creation and maintenance of traceability matrices, ensuring all system requirements are covered by verification activities - Provide technical feedback and drive continuous improvement of verification processes and practices Requirements - Bachelor’s or Master’s degree in Engineering or a related technical field - 5+ years of experience in system verification and validation within a regulated industry, ideally medical devices - Experience working with complex embedded systems (hardware, firmware, software) and performing system-level testing, such as EMC, electrical safety, environmental tests - Strong familiarity with IEC 60601 series standards (IEC 60601-1, IEC 60601-1-2, etc.) is highly preferred, with proven ability to translate standard requirements into verification strategies - Familiarity with regulatory frameworks such as FDA, MDR, and ISO 14971 - Hands-on experience developing and executing both manual and automated test methods - Excellent collaboration and communication skills, with the ability to work effectively across hardware, firmware, software, quality, regulatory, and external partner teams - Good documentation skills and proficiency in English About titles at Neko We use a simplified internal title framework that prioritises clarity over hierarchy, so internal titles may differ from market‑facing role titles. Scope, impact and level of the role are fully aligned and will be clearly discussed throughout the process. Hiring Process Candidates progress from application and structured screening through thoughtfully designed interviews culminating in a formal offer and final pre-employment checks before joining the team. Equal Opportunity & Inclusion Statement Neko Health is committed to inclusive hiring and member-first care. We welcome candidates from all backgrounds and encourage you to request reasonable adjustments to support your application.