Medical Device Lead Auditor - Freelance

WE PULL MEDICAL TECHNOLOGY FROM THE FUTURE TO SOLVE HUMAN HEALTH.

The company 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.

ABOUT THE ROLE

As a Freelance Medical Device Lead Auditor at the company, 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 the company’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 the company’s notified body activities. This is a fully remote role, with flexible scheduling, subject to audit demand and availability.

RESPONSIBILITIES

• Conduct remote audits of medical device manufacturers’ Quality Management Systems under ISO 13485, ISO 27001, ISO 42001, EU MDR, and UK MDR.

• Provide clear, structured audit documentation and evidence-based conclusions.

• Contribute to consistent, high-quality audit experiences aligned with the company’s audit methodology and values.

REQUIRED QUALIFICATIONS

• 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

• ISO 27001

• ISO 42001

• 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 the company’s values, audit methods and tooling.

PREFERRED QUALIFICATIONS

• Practical experience working with software.

• Experience with software medical devices (SaMD).

INTERVIEW PROCESS

• Introductory call with Emily [link for members] (30 min)

• Auditor competence & regulatory interviews (2x30-45 min)

• References

• Offer & onboarding