Jobs at Neko Health

As a Data Engineer, you will design and build data pipelines, models, and infrastructure for analytics and machine learning while ensuring data quality and compliance.

As a Lead Software Engineer, you'll design and build user experiences, architect features, drive reliability initiatives, and mentor other engineers, ensuring member systems are robust and scalable.

The Director of Platform Engineering will architect and build Neko Health’s internal AI developer platform, enhancing engineering workflows and driving substantial platform adoption across teams over the first year.

As a nurse at Neko Health, you will perform clinical examinations, ECGs, blood sampling, and manage documentation while ensuring quality healthcare for members.

The Workforce Planning Coordinator will oversee workforce strategy, scheduling, and coordination of staff across clinics, ensuring efficient staffing and adherence to local laws.

The Software Design QA Lead will ensure quality and regulatory compliance of SaMD and AI-enabled healthcare products, focusing on modern QA practices and collaboration with engineering teams.

As a Biomedical Scientist, you will operate advanced analysers, ensure quality control, and deliver rapid, accurate test results in a clinical setting.

The Electronics Design Engineer will design and own electronics for medical systems, focusing on PCB design, component integration, and cross-functional collaboration.

As a Senior Biomedical Scientist, you ensure accurate laboratory results, oversee operations in clinics, supervise staff, and troubleshoot technical issues while adhering to quality standards.

The role involves providing regulatory guidance for cardiology medical devices, preparing technical documentation, supporting FDA submissions, and conducting compliance audits.

The Regulatory Affairs Engineering Lead will manage regulatory documentation and submissions for dermatological medical devices, ensuring compliance with EU MDR and FDA regulations, while collaborating across teams for product development and post-market activities.

The Clinical Lab Technologist Supervisor leads the establishment and operation of a clinical laboratory, ensuring compliance with regulations and quality standards while managing validation and operational workflow.

Lead local growth and activation for Neko in Birmingham by building community, influencer and partner relationships; run B2C events and activations; support B2B initiatives; drive bookings and retention; create local reporting and a city activation playbook; align with clinical, operations, and marketing teams.

Lead local growth and activation for Neko's London clinic by building community, partnerships, and events to drive B2C bookings and B2B awareness. Own local strategy, stakeholder relationships, performance reporting, and a city activation playbook for global rollout.

Lead local growth and activation for Neko in Manchester: build community, influencer and partner relationships; run B2C events and activations; support B2B initiatives; optimize bookings, retention and reporting; create a city activation playbook and align cross-functional teams for execution.

Provide high-level administrative support to a C-suite executive: manage calendars, inboxes, travel, off-site coordination, meeting materials, and improve administrative workflows across cross-functional teams.

Build, productionize, and maintain scalable MLOps components and inference workflows for healthcare sensor data. Establish experiment tracking, model lifecycle, reproducibility, monitoring, and compliance best practices. Partner with clinical, data, and platform teams to deploy reliable, monitored ML systems aligned with healthcare-grade reliability and regulatory requirements.

Build and lead Neko's US regulatory affairs function: establish processes, SOPs and an in-region QMS; manage FDA engagement and device submissions; serve as US Agent/Initial Importer/Distributor; support state-by-state expansion and post-market regulatory activities; shape US and global RA strategy and scale the regional team.

Lead and build Neko's EMEA regulatory affairs function from the UK. Serve as UK Responsible Person, manage MHRA relationships, drive CE marking and post-market activities, create SOPs and QMS, and shape EMEA/global RA strategy for country-by-country expansion.

Provide preventive health screenings using non-invasive imaging and AI decision support, create personalized action plans, educate members on risk and lifestyle, oversee APPs and clinical escalations, and collaborate with cross-functional teams to improve member outcomes and experience.