Teams 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.

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.

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