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.

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.