Informatiq Consulting Limited

Informatiq comes to London

We're excited to announce the launch of our London office.

More details...

Medical Devices Lead Auditor - ISO13485

Medical Devices Lead Auditor - ISO13485

UK Wide

55k + Car + Benefits


Elaine Taylor

01923 224481

Add to job cart

Send to a friend

Print (opens new window)

Apply now

Medical Devices Lead Auditor - ISO13485

If you are an experienced Medical Devices Lead Auditor and want to work for a credible organisation with a good work life balance relative to the position then this could be right up your street.

This position offers lots of opportunity for personal development and is for someone who wants to follow a career in auditing and who is keen to develop further. Yes you need to travel but it won't encroach on your weekends as happens with some roles in this line of work.

ISO 13485, MDD 93/42/ECC

Home Based with travel
Excellent Package incl Car , Healthcare and Pension

You will join a major player in the Certification Services / Training Sector, and become one of their credible specialist Medical Devices Lead Auditors. You will conduct external audits for clients required to meet the ISO13485 standard and other criteria required when manufacturing medical devices.

Based from home you will be required to visit clients to assess their quality systems to national and sector relevant regulations and standards, such as ISO13485 , MDD 93/42/ECC.

As Medical Devices Lead Auditor you will be producing high quality assessment reports and reflecting business assurance principles in compliance with accreditation requirements. As part of the role you will pass client feedback on pointing out both minor and major non-conformances, and where required initiating improvement projects as required.

For this particular position I need candidates who have Medical Devices audit expertise , including an in-depth knowledge of the ISO13485 Standard .

Key requirements for Medical Devices Lead Auditor are:

A strong Quality Assurance background with recent experience working either in a Quality Management or Lead Auditor position.
Experience of working in a highly regulated medical devices manufacturing environment with a knowledge of standards and regulations.
Ideally you will need to be a Registered Lead Auditor
Proven experience of the assessment of ISO13485.
Strong Client Facing expertise

This position will see you auditing quality and management systems on client site and therefore requires a 1st class professional manner and exceptional communication skills.

If you fit the bill don't delay apply now!

Search for jobs Search explained

ISO 9001 logo; Sunday Times Top 100 link; REC logo