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Quality Engineer

Newton Colmore
Posted a day ago, valid for 13 days
Location

Walsall, West Midlands WS11XR, England

Salary

£30,000 - £36,000 per annum

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Contract type

Full Time

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Sonic Summary

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  • An established Medical Devices company in Walsall is seeking a Quality Engineer to support CAPA processes, document control, and supplier management.
  • Candidates should have experience in Medical Devices to ISO 13485 standards, with a preference for those who have quality assurance inspection testing experience.
  • The role is open to applicants with a couple of years of experience in ISO 13485 or QMS, as well as those with more extensive backgrounds.
  • A degree related to Quality Assurance, Quality Engineering, or Design Assurance is required, and familiarity with Regulatory Affairs is advantageous.
  • The position offers a competitive salary, and candidates are encouraged to apply promptly due to high interest in the role.

Quality Engineer - Walsall

An established Medical Devices company based in the Walsall area is currently looking for a new Quality Engineer to assist with the teams CAPA processes, document control and supplier management. They are specifically looking for someone who has worked in Medical Devices to ISO 13485 standards.

You will be creating and managing technical files for several Medical Devices lines. You'll collaborate with a number of Medical Devices experts. However, you will receive Quality Assurance assistance from the parent company's Quality Assurance & Regulatory Affairs Manager. Due to this, we are open to candidates who only have a couple of years of experience of ISO 13485 or QMS, but also keen to hear from people with more experience.

A key area of experience that is needed for this role is quality assurance inspection testing, so please make this experience clear on your CV.

This is an excellent opportunity for someone a couple of years into their career and looking for more responsibility to lead the development of their career.

You will ideally need to be in the office daily, however they will consider candidates who need one day a week hybrid.

It is expected that you would hold a degree in a subject that has led you into a Quality Assurance, Quality Engineering, or Design Assurance role.

Apart from having a Quality Assurance background, it would also be highly advantageous if you have a good understanding of Regulatory Affairs.

Part of your role will involve working alongside the manufacturing teams for these medical devices. Due to this, it would be highly beneficial if your Medical Devices Quality Assurance experience came from a Quality Engineering background, although this is not essential.

I anticipate a lot of interest in this role, so if you are interested, I suggest making an application now or risk missing out.

For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on (phone number removed) or make an application and one of our team at Newton Colmore Consulting will contact you.

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