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Quality Engineer

Newton Colmore Consulting

Walsall

Hybrid

GBP 30,000 - 50,000

Full time

23 days ago

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Job summary

An established medical devices company is seeking a Quality Engineer to enhance their CAPA processes and document control. This role offers a fantastic opportunity for those early in their career looking to take on more responsibility. You will be involved in creating technical files and collaborating with industry experts while receiving support from the Quality Assurance & Regulatory Affairs Manager. Ideal candidates will have experience with ISO 13485 standards and a background in quality assurance. This position allows for a hybrid work arrangement, making it an attractive opportunity for aspiring quality professionals.

Qualifications

  • Experience with ISO 13485 standards is essential for this role.
  • Background in Quality Assurance or Quality Engineering is preferred.

Responsibilities

  • Manage CAPA processes and document control for medical devices.
  • Collaborate with experts and assist in quality assurance inspections.

Skills

ISO 13485
Quality Assurance
Document Control
Supplier Management
Quality Engineering
Regulatory Affairs
Quality Inspection Testing

Education

Degree in Quality Assurance
Degree in Quality Engineering
Degree in Design Assurance

Job description

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 team's 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 +44 121 268 2240 or make an application and one of our team at Newton Colmore Consulting will contact you.

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