Jobs at CoMind

As Electronics Engineering Manager, you will lead FPGA development and design complex electronics systems, managing a team while ensuring regulatory compliance and high-quality standards.

Lead end-to-end technical recruitment across hardware, software, and engineering teams in the UK and US. Build and manage talent pipelines, maintain ATS/data integrity, conduct market mapping and competitive intelligence, partner with People Ops on compliant offers and onboarding, and improve TA processes. Drive sourcing for senior and hard-to-find talent and maintain hiring metrics and reporting.

Serve as technical authority for signal processing and ML for CoMind One: define methodologies, develop and validate algorithms for cerebral blood flow, intracranial pressure, and autoregulation, drive data collection and labelling, produce regulatory evidence, publications and patents, and represent data science across R&D, clinical, and engineering teams. Senior individual contributor based in Kings Cross (4 days/week onsite).

Generalist People Partner supporting UK HQ and remote US team. Responsibilities include manager coaching, designing and delivering training, independent ER case management, HRIS ownership (HiBob), payroll co-ownership, onboarding/offboarding, contractor administration (IR35), policy maintenance, and leading wellbeing programmes across UK and US.

Lead and mentor an optical engineering team to design, build, and validate laser interferometry-based photonic systems for a medical neuromonitoring device. Own optical design, modelling (Zemax/COMSOL), tolerance analysis, integration with mechanical/electronic subsystems, manufacturing transfer, supplier management, and compliance with ISO 13485/IEC 60601-1. Contribute technically and drive V&V, design reviews, and production readiness.

Lead and mentor an optical engineering team to design, build, and validate laser interferometry-based photonic systems for a medical device. Drive optical design, modelling, tolerance analysis, V&V, supplier/manufacturer handover, and cross-functional integration within ISO 13485/IEC 60601-1 design controls.

Define and architect end-to-end verification and compliance-as-code for a medical device software stack. Build scalable test infrastructure across embedded and cloud systems, integrate safety and regulatory evidence into CI/CD, lead AI-augmented test strategies, mentor engineers on TDD and automated quality gates, and collaborate with Systems and Regulatory teams to ensure IEC 62304 and ISO 14971 compliance.

Lead embedded and real-time C++ development for a regulated medical device: design hardware abstraction, device drivers, and data acquisition; define technical strategy; ensure IEC 62304-compliant software quality; collaborate with FPGA/electronics teams; mentor engineers; contribute to risk management and system integration in a safety-critical clinical environment.

Lead system-level requirements, architecture, integration, and V&V for a non-invasive neuromonitoring medical device. Manage requirements baselines and traceability, define system architecture and interfaces across hardware, software, and optical subsystems, drive integration and verification campaigns, support ISO 14971 risk management and regulatory evidence generation, and maintain systems engineering processes and tooling.

Lead and grow a mechanical engineering team to design, validate, and transfer precision mechanical and optomechanical medical device hardware to production. Contribute hands-on to CAD modelling, tolerance analysis, FEA, DFM/DFA, and cross-functional integration. Manage contract manufacturer relationships and ensure compliance with design controls, QMS, ISO 13485, and IEC 60601-1.

Lead design, modelling, and validation of precision optical subsystems (interferometry, beam delivery, stray light control). Drive experimental characterization, supplier collaboration, component selection, integration with mechanical/electronic subsystems, and regulatory documentation in line with ISO standards for medical devices.

Design, author, and execute verification and validation test protocols across hardware, firmware, and software for a regulated medical device. Develop and qualify test methods/equipment, analyse results, report anomalies, maintain traceability matrices, support system integration and ISO 14971 risk activities, and produce regulatory-standard verification reports.

Lead design, modelling, and experimental validation of optical subsystems for a medical laser-interferometry sensing platform. Drive component selection and supplier collaboration, develop optical simulations, perform precision alignment and characterisation, integrate optics with mechanical/electronic subsystems, contribute to design reviews and regulatory documentation (ISO 14971/13485/IEC 60601-1), and support transition to manufacturable hardware.

Lead and grow a multidisciplinary hardware engineering team to deliver regulated medical device products from translational research through commercialization. Own hardware standards, processes, regulatory alignment (FDA, ISO 13485, IEC 60601), cross-functional delivery, and technical strategy for mechanical, electronics, and opto-mechanical systems.

Lead end-to-end delivery of a complex multidisciplinary medical-device sub-system across optics, electronics, mechanical, FPGA, and software. Own integrated planning, schedule, RAID, resourcing, partner management, regulatory design-control compliance, budgets and reporting to drive design maturation, verification, and transfer in a fast-paced startup.

Lead electronics and FPGA development for a medical neuromonitoring device: design mixed-signal circuits, multi-layer PCBs, FPGA RTL/DSP pipelines, verification, manufacturing transfer, regulatory compliance, and manage a team of engineers.

Own architecture and end-to-end design of precision analogue and mixed-signal electronics for neuromonitoring medical devices. Lead low-noise front-end, ADC/DAC interfaces, high-speed digital/PCB design, verification, EMC/safety compliance, manufacturing release, documentation, and mentor engineers.

Lead architecture, design, verification, and production release of FPGA systems for a regulated medical device. Build real-time data acquisition, DSP, and high-speed interfaces, drive platform selection and timing/power closure, support hardware bring‑up and validation, maintain regulatory traceability, and mentor engineering staff.

The Optical Test Engineer will design test plans, build characterization rigs, develop SOPs, and analyze data for non-invasive brain monitoring technology at CoMind.

Own day-to-day finance operations for UK and US entities, manage bookkeeping, month-end close, reporting, budgeting, payroll support, tax and audit coordination, vendor payments, process improvement, and apply AI tools to modernize finance workflows.