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Device Specialist

Open 25d

Summary

Audits and certifies innovative medical devices for regulatory compliance, focusing on software and hardware, while optimizing assessment processes and staying current with global standards.

We pull medical technology from the future to solve human health.

Authorised by governments around the world to assess medical AI, we remove unnecessary delays from every regulatory approval we do so patients get devices from the future, today. We are proud to count the world’s most ambitious companies building medical technology as customers. You will be joining a team with product-market fit, flowing data, and exponentially growing revenue.

About this role:
Scarlet’s Devices function is a team of clinicians, software engineers and device specialists, working together to audit, assess and certify the most innovative and impactful medical devices.

We pride ourselves on delivering efficient audits and fast technical assessments to enable market access, new device updates and ongoing surveillance of a growing portfolio of medical devices.

We are both the designers and operators of our auditing and assessment processes, working with Scarlet's internal team of software developers, product designers, and ML engineers, to develop world-class tooling to support conformity assessment.

We’ve proven our capabilities with medical device software and are actively expanding our scope to include hardware medical devices.

Your responsibilities:

  • Get authorised to audit management systems and assess the technical documentation of the most innovative devices in the world.

  • Collaborate with product, engineering, and ML to optimise our processes and continue to scale them.

  • Collaborate with teammates in the operations function to expand the scope of Scarlet’s approvals to enable our customers to reach more people.


Key skills:

  • You've got a bachelor’s degree or higher in engineering, medicine or other relevant science or engineering discipline

  • You've worked for 4+ years designing, building and/or researching medical devices

  • You've got 2+ years of experience with quality management systems

  • You have experience in software design, verification and validation

  • You feel comfortable with reading normative texts and analysing and interpreting requirements to extract the essential information

  • You like going down rabbit holes, understanding deeply how things work, and challenging the status quo

  • You have worked in different environments and like operating with autonomy on sometimes ambiguous tasks

  • You have exceptional written & verbal communication skills


The interview process:

  1. Intro call with Sandy - 30 mins

  2. Team interviews - 2 x 30 mins

  3. Technical interview - 1 hour

  4. Culture and values interview with James and Jamie - 2 x 30 mins

  5. Referencing & offer

What this application asks

ashby

Name, Email, Resume

  • LinkedIn Profile optional
  • Location
  • Right to Work yes / no
  • Why Scarlet? written answer · optional
  • Quality management experience written answer · optional
  • Device design/manufacture experience written answer · optional

See also

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