MedTech Device Compliance Auditor (AI/Software & Hardware)

MedTech Device Compliance Auditor (AI/Software & Hardware)

Full-Time 45000 - 55000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Audit management systems and assess technical documentation for innovative medical devices.
  • Company: Scarlet, a forward-thinking MedTech company based in London.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Dynamic role with a focus on both software and hardware certifications.
  • Why this job: Join a team at the forefront of technology and make a difference in healthcare.
  • Qualifications: Bachelor’s degree and experience in medical device manufacturing and quality assurance.

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

Scarlet, based in London, is seeking a Device Specialist to audit management systems and assess technical documentation for cutting-edge medical devices. This role sits in the London Assessment team, bridging regulatory standards with frontier technology and expanding Scarlet's scope from software into hardware certifications.

The ideal candidate holds a Bachelor’s degree in a relevant field and brings multiple years of experience in medical device manufacturing, design/testing, and quality.

MedTech Device Compliance Auditor (AI/Software & Hardware) employer: Jack & Jill

At Jack & Jill, we pride ourselves on being an exceptional employer that fosters a dynamic and innovative work culture. Our team enjoys a range of benefits including flexible working arrangements, professional development opportunities, and a collaborative environment that encourages creativity and growth. Located in a vibrant area, we offer unique advantages such as access to cutting-edge technology and the chance to work with industry leaders in AI-driven marketing strategies.

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Contact Details:

Jack & Jill Recruitment Team

We think you need these skills to ace MedTech Device Compliance Auditor (AI/Software & Hardware)

Auditing Skills
Regulatory Standards Knowledge
Technical Documentation Assessment
Medical Device Manufacturing Experience
Design and Testing Experience
Quality Assurance
Bachelor’s Degree in Relevant Field