Jobs at Neko Health

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 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 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.

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.

Lead and own biochemistry and haematology services across clinic-based labs: monitor Abbott Alinity analysers, validate assays, manage quality (IQC/EQA, ISO15189/UKAS), supervise and train staff, ensure timely, accurate results, manage operations, stock, incidents, and support scaling of new laboratories.

Senior Biomedical Scientist with end-to-end responsibility for biochemistry and haematology services across clinic labs. Monitor and troubleshoot analysers, lead validations, manage quality (IQC/EQA, SOPs, audits), supervise and train staff, ensure rapid turnaround, manage stock and operations, and support scaling new UK laboratories.

Operate Abbott Alinity and Sysmex XN analysers to perform biochemistry, immunoassay and haematology testing; validate and escalate results; perform calibration, IQC/EQA and routine maintenance; work within ISO 15189/UKAS quality systems, author SOPs, support audits and investigate non-conformances; contribute to verification, reagent evaluation and software testing; maintain records and KPIs; provide technical guidance and training.

Lead and manage the global customer support function, establishing strategies, standards, and architecture for exceptional member support across markets. Drive transformation and performance metrics while integrating AI to enhance service delivery and team efficiency.

The role involves leading communication strategies, managing media relations, supporting brand storytelling, and mentoring a communications team to enhance brand impact.

Operate Abbott Alinity and Sysmex XN analysers to deliver rapid, accurate diagnostic results within a UKAS/ISO 15189-aligned quality system. Perform daily calibration, IQC/EQA, routine maintenance, troubleshooting, SOP authorship, audit support, analyser verification, LIMS-related activities, and provide technical guidance and training to clinical colleagues to support fast-turnaround preventive health screening.

As Communication Lead for Sweden, you will drive brand messaging, public relations, and content strategy while leading a high-performing communications team.

Provide preventive health screenings using non-invasive imaging and cardiovascular assessments, create personalized action plans, educate members on risks and lifestyle changes, escalate findings to supervising physicians, and collaborate with cross-functional teams to ensure high-quality member experience.

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.

The Cardiology GP interprets ECG and echocardiogram results, manages cardiac aftercare, escalates urgent findings, and collaborates with clinical teams in the UK.

As an Echocardiographer, you'll perform independent echocardiographic assessments, interpret results, integrate findings into health assessments, and engage in quality assurance and professional development activities.

Lead development of global FF+E standards, product selection, and procurement strategy. Create playbook guidance, manage vendor sourcing and quality, and drive bespoke product development across regional projects to ensure cohesive, scalable member experiences.

Perform independent transthoracic echocardiograms (including GLS), produce same-session reports, follow escalation protocols, collaborate with cardiology and multidisciplinary teams, participate in QA and protocol development, and support imaging equipment troubleshooting across NYC clinics.

Reconcile Quinyx scheduling and timesheet data against payroll, prepare variable-hours pay data (overtime, uplifts, premiums), maintain shift patterns and pay rules, resolve payroll queries with frontline staff and managers, and propose process improvements over a six-month FTC.

Lead regulatory strategy and hands-on regulatory engineering for AI/ML-powered SaMD across EU MDR, FDA, and UK MDR. Prepare submissions and technical files, embed IEC 62304 and EU AI Act obligations into development workflows, support change control and post-market surveillance, train teams, and participate in audits and agency/notified body interactions.

The Director of Financial Control will establish a robust financial control framework, standardize accounting policies, and build a high-performing global finance team to support international growth and compliance readiness.