An established Medical Devices company based in the Walsall area is currently looking for a Quality Engineer to assist with the team's CAPA processes, document control, and supplier management. They are specifically seeking someone with experience in Medical Devices aligned with ISO 13485 standards.
The role involves creating and managing technical files for multiple Medical Devices lines. You will collaborate with Medical Devices experts and receive Quality Assurance support from the parent company's QA & Regulatory Affairs Manager. Candidates with a few years of ISO 13485 or QMS experience are encouraged to apply, as well as those with more extensive experience.
A key requirement is experience in quality assurance inspection testing, which should be clearly highlighted on your CV.
This is an excellent opportunity for someone early in their career seeking more responsibility to advance professionally.
Ideally, you should be able to work in the office daily; however, a hybrid arrangement (one day a week) will be considered.
You are expected to hold a degree related to Quality Assurance, Quality Engineering, or Design Assurance. Additionally, a good understanding of Regulatory Affairs would be highly advantageous.
Experience working alongside manufacturing teams in Medical Devices QA from a Quality Engineering background is preferred but not mandatory.
If interested, I recommend applying promptly to avoid missing out.
For more information, please contact Andrew Welsh, Director of Medical Devices recruitment at Newton Colmore Consulting, at +44 121 268 2240, or apply directly, and our team will get in touch.
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Created on 29/06/2025 by TN, United Kingdom.
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