Regional Regulatory Affairs Lead, EMEA

About Neko Health

Neko is redefining preventive healthcare with data-driven insights.

What you'd do

• Set up EMEA RA function processes
• Manage UK Responsible Person responsibilities
• Build a scalable country-by-country expansion process
• Align regulatory positions across jurisdictions

What they're looking for

• 8+ years in medical device regulatory affairs
• 5+ years focused on UK, EU, or EMEA devices
• Experience with CE marking under EU MDR
• Direct authority engagement with MHRA

Perks

• A voice in global regulatory decisions
• Real ownership of the UK & EMEA market
• Work with a seasoned team in Sweden