2 months ago
London, United KingdomSenior
Responsibilities
- Build compliance-as-code workflows that map verification evidence to regulatory standards and generate evidence automatically.
- Own test plans, protocols, and execution reports for medical device software.
- Drive formal software verification and validation in accordance with IEC 62304 Class C and ISO 14971.
- Advance test automation, CI/CD pipelines, build systems, and new testing techniques, including LLM-assisted quality gates.
- Test multi-tasking systems and signal-processing applications on real hardware in collaboration with systems engineers.
Requirements
- At least 5 years of software testing experience, particularly with complex or safety-critical systems.
- Proficiency in Python.
- Experience working in highly regulated industries, preferably medical device development.
- Strong hands-on experience with CI/CD, test automation, and build systems.
- Strong hands-on experience with Test-Driven Development and Behaviour-Driven Development.
Benefits
- Company equity plan.
- Salary-sacrifice pension scheme.
- Private medical, dental, and vision insurance.
- Group life insurance.
- Comprehensive mental health support with access to one-to-one sessions.
- Unlimited holiday allowance plus bank holidays and one week of remote working per quarter.
- Daily lunch vouchers and free dinner when working late.
- Fresh fruit, snacks, and drinks delivered twice weekly.
- YuLife subscription with discounts tied to daily steps and meditation.
- At least four days per week in the Kings Cross office, plus one flexible work-from-home day.
About CoMind
CoMind builds non-invasive brain-monitoring hardware and AI software for hospital clinicians, using light-based neuroimaging to capture multidimensional brain activity. The company designs and manufactures its device and the CoVision analytics platform, supporting care in intensive care, surgery, and emergency settings. Privately held and founded in 2018, CoMind is headquartered in London and develops regulated medical devices for FDA clearance and CE marking.