About the role
At CoMind, we are developing a non-invasive neuromonitoring technology that will result in a new era of clinical brain monitoring. In joining us, you will be helping to create cutting-edge technologies that will improve how we diagnose and treat brain disorders, ultimately improving and saving the lives of patients across the world.
The Role: The Product Assurance team at CoMind is responsible for ensuring the device performs as intended against its specified
requirements, generating the test evidence needed to support regulatory submissions and design history files. Working across hardware, software, and integrated system levels,
the team designs and executes test methods and protocols that demonstrate design outputs meet design inputs to the standard required for FDA clearance and CE marking. As a Verification Test Engineer, you will own the design and execution of V&V test activities for CoMind’s device, working across hardware, software, and system levels. You will develop test protocols, validate the test methods and equipment, execute testing, analyse and collate results, and author reports for a regulated medical device, working closely with systems engineering and quality throughout. As a member of the Product Assurance team
the role reports into the Systems and V+V Manager. You will have a good scientific and engineering background with a rigorous and systematic approach to problem solving, product testing and product integration. At CoMind, all team members work at least 4 days per week in the office, plus a flexible work-from-home day. This role is based in our London (Kings Cross) office.
Responsibilities: Design, write, and execute test protocols for hardware, software, and system-level design verification testing Develop and qualify test methods, test equipment and protocols against system and sub-system
requirements Collate and analyse test results, identify and report anomalies and non-conformances, and work with quality and engineering teams to investigate root causes and determine disposition Author verification test reports to the standard required for design history files and regulatory submissions, including FDA clearance and CE marking Maintain
