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Lead Auditor

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Remote

Lead Auditor

Scarlet

Lead Auditor

Skills

Cybersecurity

10 months ago

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Important information


Work mode:

Remote

Published on:

7 October 2026

What they need


Who you are

  • A bachelor’s degree in either:
  • Software engineering
  • Computer science
  • Physics or biophysics
  • Biology or microbiology
  • Chemistry or biochemistry
  • Electrical, electronic, mechanical engineering or bioengineering
  • Human physiology
  • Medicine
  • Pharmacy
  • Minimum 4 years of experience in the medical device industry
  • Minimum 2 years of experience auditing or managing QMSs under:
  • ISO 13485
  • EU MDR and/or UK MDR
  • Prior work with notified bodies or accreditation bodies as a Lead Auditor
  • Working knowledge of relevant standards, such as:
  • ISO 14971
  • IEC 62304
  • IEC 82304
  • Cybersecurity
  • Evidence of confidently interpreting and applying regulatory requirements
  • Evidence of delivering consistent, high-quality audits
  • Ability to explain findings and requirements clearly and constructively
  • Ability to deliver audits independently with minimal oversight
  • Willingness to adopt Scarlet’s values, audit methods and tooling
  • Practical experience working with software
  • Experience with software medical devices (SaMD)

What the job involves

  • As a Lead Auditor - Contractor at Scarlet, you will independently deliver efficient, high-quality QMS audits that help innovative medical device companies meet the highest regulatory standards
  • We’re expanding our auditor pool, and we're looking for part-time/contractor lead auditors who can independently deliver audits in line with Scarlet’s standards, approach and culture
  • This role is suited for auditors who fulfil the relevant criteria to be authorised as a Lead Auditor in a Certification or Notified Body under ISO 13485, EU MDR and UK MDR. You will work flexibly, supporting audit delivery as part of Scarlet’s notified body activities. This is a fully remote role, with flexible scheduling, subject to audit demand and availability
  • Conduct remote audits of medical device manufacturers’ Quality Management Systems under ISO 13485, EU MDR, and UK MDR
  • Provide clear, structured audit documentation and evidence-based conclusions
  • Contribute to consistent, high-quality audit experiences aligned with Scarlet’s audit methodology and values

The application process

  • Introductory call with Emily (30 min)
  • Auditor competence & regulatory interviews (2x30-45 min)
  • References
  • Offer & onboarding

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