We pull medical technology from the future to solve human health.
Scarlet is authorised to assess and certify medical devices.
We combine clinical, technical and regulatory expertise with AI agents and software so rigorous certification can keep pace with product development at the world’s most ambitious technology companies, without lowering the safety bar.
Our customers have cut a year or more from their certification timelines for new AI-enabled medical devices and shortened product-update cycles from months to weeks.
You’ll join a team building the infrastructure that makes these outcomes repeatable at scale.
You will become a regulatory expert capable of meeting the complex needs of our customers.
Your work will help ambitious medical technology companies bring safe products to patients sooner and drive Scarlet’s growth.
This is a London-based role with a global reach.
What you'll be working onThe companies you'll be selling to are doing some of the most interesting work in healthcare right now.
A few of the customers you'll be pointing prospects towards:Floy certified three AI radiology devices under EU MDR, completed an ISO transfer and a scope extension, all in 16 weeksSkin Analytics brought a Class III AI dermatology device to the European marketAugmedit certified multiple augmented reality neurosurgery devicesFlok Health went from submission to EU MDR certification of an AI physiotherapy device in 14 weeksLucida Medical transferred an AI radiology device to Scarlet in seven weeks and started shipping model updates immediatelyFeebris got an AI photoplethysmography device certified in time to support critical NHS prioritiesYou can read all of these at scarlet.
cc/customer-stories.
Your job is to find the next Floy or Skin Analytics and show them there's a faster way.
ResponsibilitiesBuild and nurture rela.