Medical Device QMS Auditor & Compliance Engineer in London

Medical Device QMS Auditor & Compliance Engineer in London

London Full-Time 45000 - 55000 Β£ / year (est.) No working from home possible
Meeveem Limited

At a Glance

  • Tasks: Audit and certify Quality Management Systems for medical devices and design efficient audit workflows.
  • Company: Scarlet, a leading healthtech company in Greater London.
  • Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
  • Other info: Exciting opportunity to work with innovative healthtech products.
  • Why this job: Join a dynamic team making a real difference in the healthtech industry.
  • Qualifications: Bachelor's in engineering or sciences, 4+ years in medical devices, and proven audit experience.

The predicted salary is between 45000 - 55000 Β£ per year.

Scarlet is seeking a regulatory-focused Quality Auditor to join its Medical Device Quality Team in Greater London.

You will audit and certify QMS against ISO 13485, EU MDR and related standards, and help design efficient audit workflows for healthtech products.

Ideal candidates have a Bachelor's in engineering or sciences, 4+ years in medical devices, 2+ years in quality management and proven audit experience.

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Medical Device QMS Auditor & Compliance Engineer in London employer: Meeveem Limited

Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.

Meeveem Limited

Contact Details:

Meeveem Limited Recruitment Team

We think you need these skills to ace Medical Device QMS Auditor & Compliance Engineer in London

Quality Management Systems (QMS)
ISO 13485
EU MDR
Audit Experience
Healthtech Product Knowledge
Workflow Design
Regulatory Compliance