Regulatory Specialist

Senior Regulatory Affairs Specialist – Neurovascular Medical Devices
EU or UK (Remote)
Direct Contract 

We're working with a growing international medtech business that’s building out its EMEA regulatory function and looking to hire its first RA/QA person in Europe.
This is a genuinely interesting one, a hands-on role with a lot of ownership, where you’ll be the go-to for EU MDR across a neurovascular portfolio, with a clear path to build and lead a team over time.

The role

You’ll be leading EU MDR strategy and submissions for Class III neurovascular devices (aneurysm coils, stents, flow diverters), supporting expansion of CE-marked products.
You’ll work closely with the Shanghai HQ (where RA/QA currently sits), but own things on the ground across EMEA, working with distributors across ~22 countries.
There’s also a secondary QMS angle, so it’s a bit of a multi-hat role.

What they’re looking for

• Solid EU MDR experience 
• Ideally neurovascular / neuro-interventional background
• Experience with Class III devices
• Comfortable working in a lean, international setup
• Someone happy being hands-on but who wants to grow into a leadership role

Setup

• Remote (EU or UK)
• Team currently ~6 in EU/UK + external partners

Feel free to reach out directly with your CV or message Aimee Brenner at a.brenner@panda-int.com for more details.