Quality Engineer

Newton Colmore Consulting Ltd; United Kingdom; Hybrid; GBP 30,000 - 50,000; Full time

Job summary

An established Medical Devices company in the Walsall area is seeking a Quality Engineer to enhance their CAPA processes and supplier management. This role is perfect for someone with a couple of years of experience in ISO 13485 standards, looking to take on more responsibility and advance their career. You will be involved in creating and managing technical files while collaborating with Medical Devices experts. The company offers a hybrid work option, allowing flexibility while ensuring you gain valuable experience in quality assurance and regulatory affairs. Don't miss this opportunity to grow in a dynamic environment!

Qualifications

• Experience in ISO 13485 and Quality Assurance is essential.
• Degree in a relevant field is required for this role.

Responsibilities

• Manage technical files for Medical Devices and assist with CAPA processes.
• Collaborate with experts and support manufacturing teams.

Skills

ISO 13485

Quality Assurance

Regulatory Affairs

Quality Engineering

Document Control

Supplier Management

CAPA Processes

Quality Inspection Testing

Education

Degree in Quality Assurance or related field

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