S
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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