C

Regulatory Submission Lead – Medical Devices

Cpl Life Sciences

London, England, United Kingdom FULL TIME June 18, 2026
Apply Now

Opportunity Description

Overview

Regulatory Submissions Lead


Location: UK (remote)


Salary: Up to £80,000

Cpl Life Sciences is partnering with a small but growing medical device business that has recently secured funding and is now looking to hire a Regulatory Submissions Lead to support its next phase of growth. This is a hands-on role with real ownership — ideal for someone who enjoys working across strategy and execution in a fast-moving environment.

You’ll be responsible for leading regulatory submissions across the UK, EU, and US, including FDA 510(k), De Novo, and Q-Subs, while acting as a key point of contact for regulators and notified bodies. Alongside submissions, you’ll play a big part in shaping regulatory strategy, ensuring compliance across the full product lifecycle, and supporting the business as it expands into new markets.

Key Responsibilities

  • Lead global regulatory submissions (FDA, EU MDR, UKCA)

  • Prepare and...
  • FULL TIME Healthcare Diagnosing or Treating Practitioners

    Ready to Apply?

    Submit your application for Regulatory Submission Lead – Medical Devices at Cpl Life Sciences

    Apply for this Position