
Job Overview
Location
London, UK
Job Type
Full-time
Category
Software Engineering
Date Posted
June 21, 2026
Full Job Description
📋 Description
- • Design, write, and execute hardware, software, and system-level verification test protocols for a regulated medical device to ensure compliance with design inputs and regulatory standards for FDA clearance and CE marking.
- • Develop and qualify test methods, equipment, and protocols against system and sub-system requirements, ensuring repeatability and traceability throughout the verification lifecycle.
- • Collate, analyze, and interpret test results; identify and document anomalies and non-conformances, and collaborate with quality and engineering teams to investigate root causes and determine appropriate dispositions.
- • Author comprehensive verification test reports that meet regulatory documentation standards for design history files, including detailed evidence for FDA and CE regulatory submissions.
- • Maintain and update requirements traceability matrices to ensure full test coverage, proactively identifying and resolving gaps prior to design reviews and regulatory milestones.
- • Support system integration testing by coordinating execution across hardware, firmware, and software components, and accurately documenting integration test outcomes and dependencies.
- • Contribute to risk management activities under ISO 14971 by reviewing FMEAs and verifying the effectiveness of implemented risk controls through test evidence.
- • Develop and maintain test infrastructure, including fixtures, calibration records, and tooling, to ensure efficient, repeatable, and auditable verification activities.
- • Utilize Python to develop software-based test tools and scripts for automated data collection, analysis, and reporting in verification workflows.
- • Work closely with systems engineering and quality teams throughout the product development lifecycle to align verification activities with design outputs and regulatory expectations.
- • Embrace AI as a core part of daily work, integrating it into test design, automation, data analysis, and collaboration to enhance efficiency and innovation.
- • Operate within a regulated medical device environment with strict adherence to design control processes and documentation requirements.
- • Work a minimum of four days per week in the London (Kings Cross) office, with one flexible remote day per week as part of the company’s hybrid work policy.
- • Participate in cross-functional teams to ensure verification activities are synchronized with product development timelines, regulatory submission schedules, and quality system audits.
- • Ensure all test activities are fully traceable to system requirements and documented in accordance with ISO 13485 and IEC 62304 standards where applicable.
- • Maintain accurate records of test equipment calibration status and ensure all tools used in verification are properly maintained and validated.
- • Contribute to continuous improvement of verification processes by identifying opportunities for automation, efficiency gains, and enhanced test coverage.
🎯 Requirements
- • 4+ years of experience in verification, test engineering, or a closely related role with hands-on experience writing and executing test protocols for complex hardware or software systems
- • Experience in a regulated industry (medical devices, aerospace, automotive, or similar) with familiarity with design control requirements
- • Proficiency in developing software-based test tools and scripts in Python for collecting and analyzing test data
- • Strong analytical skills to identify, investigate, and document test anomalies and non-conformances, and support root cause analysis
- • Clear and precise technical writing skills with experience authoring test protocols and reports that meet regulatory documentation standards
- • Familiarity with requirements management tooling and test management platforms
🏖️ Benefits
- • Company equity plan so all employees share in the success of the company
- • Salary-sacrifice pension scheme
- • Private medical, dental and vision insurance (medical history disregarded)
- • Group life assurance at 4x annual income
- • Comprehensive mental health support, including unlimited access to 1:1 sessions with trained professionals
- • Unlimited holiday allowance (+ bank holidays) and one week of remote working per quarter
- • Lunch voucher (£10) every day for JustEat and free dinner on days worked late
- • Twice weekly deliveries of fresh fruit and an extensive selection of snacks and drinks
- • YuLife subscription, allowing daily steps and meditation to be turned into discounts at a range of stores
Skills & Technologies
See exactly how your profile matches this role — strengths, skill gaps, and what to do about them.
About CoMind Technologies Inc.
CoMind Technologies is focused on redefining how the brain is measured and treated. They are developing non-invasive neurotechnology with the goal of optimizing patient outcomes across the care continuum. Their technology aims to provide doctors with access to a wide array of critical neurophysiological signals through a single, simple bedside measurement. CoMind Technologies is working to improve patient outcomes through photonics technology. The company recently announced $102.5 million in funding to further its mission of redefining clinical monitoring of the brain.
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