SonicJobs Logo
Login
Left arrow iconBack to search

Quality Engineer

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

Walsall, West Midlands WS4 1PL, England

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

info
  • 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 and familiarity with ISO 13485 standards, with a focus on quality assurance inspection testing.
  • The role is suitable for individuals with a couple of years of experience or more in Quality Management Systems, and a degree related to Quality Assurance or Engineering is preferred.
  • The position offers a salary of £35,000 to £45,000, depending on experience, and may allow for one day of hybrid work per week.
  • Interested applicants are encouraged to apply promptly to avoid missing out on this excellent career development opportunity.

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 + or make an application and one of our team at Newton Colmore Consulting will contact you.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.