Skip to main content
Post your CV and find your next job on Indeed!

Emea Medical Device jobs

Sort by: -
    • Experience with medical device software.
    • At least four years’ experience in the medical device industry, including two years auditing or managing an ISO 13485…
    • View all Scarlet jobs - London jobs - Auditor jobs in London
    • Salary Search: Medical Device Auditor salaries in London
    • We are looking for a Medical Device Assessor / Auditor with a background in medical device designing manufacturing, or quality control.
    • This permanent role will see you play a key part in assessing and improving Quality Management Systems for software-based medical devices.
    • The overall purpose of the role is to deliver education and training to staff including competency based medical device programmes in line with the Medical…
  • View similar jobs with this employer
    • Significant experience (typically 8+ years) within medical device industry.
    • We are seeking an experienced Medical Device Quality Specialist Consultant to…
  • View similar jobs with this employer
    • Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
    • Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
    • Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
    • A genuine interest in healthcare, science, technology or medical devices.
    • With 45 years experience in medical test technology and full facility capabilities…
    • Heartfelt Technologies is a medical device startup focused on improving patient care through innovative technologies.
    • All necessary training will be provided.
  • View similar jobs with this employer
    • Previous pharmaceutical experience is not essential, with training and development available to support those new to the industry.
    • Join a *growing, specialist medical distributor* with an established NHS customer base.
    • *3+ years' territory management experience* within medical devices or…
    • Exposure to ISO 13485 or the medical device sector.
    • At SAVA, we are rapidly scaling a next-generation biosensor designed to shift healthcare from reactive to…
    • Work closely with Medical Engineering and other areas to ensure medical equipment is available for start of theatre lists.
    • Significant experience in medical device and/or drug-device combination product development;
    • This role calls for a senior engineer with substantial experience…

People also searched:

remote first
systems
uk emea
europe
hebrew
identity
ikea
israel
mdm
medical assistant

Job Post Details

Medical Device Auditor
Scarlet
London
£75,000 - £90,000 a year
Full-time
Apply on company site

Job details

£75,000 - £90,000 a year
Full-time
London

Full job description

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


Scarlet 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 Medical Device Auditor at Scarlet based out of either our London or Sweden office, you will audit medical device manufacturers’ quality management systems and produce clear conclusions that support certification decisions. You’ll receive training in Scarlet’s audit methods and tools. Your work will combine reviewing evidence with conversations about how manufacturers’ processes work in practice. Travel will be limited, though occasional trips may be required. You will help safe devices reach patients sooner.

Responsibilities

  • Plan and conduct QMS audits against ISO 13485, EU MDR and UK MDR requirements.

  • Review records and interview teams to assess whether their processes meet the requirements.

  • Document evidence, findings and conclusions in clear, timely audit reports.

  • Explain findings constructively and keep customers informed throughout the audit.

  • Review corrective actions and the evidence needed to close findings.

Required qualifications

  • A degree in a relevant scientific, engineering or medical discipline.

  • At least four years’ experience in the medical device industry, including two years auditing or managing an ISO 13485 QMS.

  • Working knowledge of EU MDR or UK MDR requirements for quality management systems.

  • Experience explaining audit findings or regulatory requirements clearly, in writing and in conversation.

  • Experience with software demonstrating knowledge of software design, validation, testing, debugging and interactions with its operating environment.

Preferred qualifications

  • Experience conducting audits for a certification or notified body.

  • Experience with medical device software.

Interview process

  • Introductory call with Sandy — 30 minutes.

  • QMS audit exercise and discussion with Felicia — 40 minutes.

  • Founder interviews: James and Jamie (2x20 mins)

  • Offer & references

Compensation Range: £75K - £90K

Let Employers Find YouUpload Your Resume