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Quality Compliance Engineer

AVD Appoint Ltd

United Kingdom

On-site

GBP 42,000

Full time

22 days ago

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An innovative technology company in Glamorgan is seeking a Quality Assurance Engineer to enhance their internal audit processes. This role involves managing ISO:13485 audits, addressing customer complaints, and collaborating on engineering changes. With a commitment to developing cutting-edge products and a strong growth trajectory, this company offers a dynamic environment for professional advancement. If you have a passion for quality assurance and a desire to contribute to a leading firm in the industry, this opportunity is perfect for you.

Relocation Assistance

Career Development Opportunities

Comprehensive Benefits

3+ years of experience in Quality Assurance and conducting internal audits.
Familiarity with ISO:13485 standards in a medical context.

Conduct internal audits in line with ISO:13485 and manage the audit schedule.
Handle customer returns, complaints, and engineering change requests.

Quality Assurance

Internal Audits

ISO:13485

Customer Returns Management

Engineering Change Requests

CAPAs

Quality Assurance Engineer - Glamorgan - up to 42,000 + Relocation + Benefits - Ref 1888

I am currently recruiting for a Quality Assurance Engineer to work for a cutting-edge technology company based in Glamorgan. Salary up to 42,000 + Relocation + Benefits.

The organisation has been in operation for many years and are worldwide leaders within the design, development, and manufacture of their highly intelligent products. As a business they turnover north of 85m, employ 500 people and are constantly evolving their legacy products as well as designing and developing new innovative products to bring to market.

In line with demand for their products and to support the business with their growth plans they have the need to appoint another Quality Assurance Engineer on a permanent basis.

In this role as a Quality Assurance Engineer, you will be responsible for the internal audits within the company in line with ISO:13485. This will involve you setting up the audit schedule and then owning it through the process raising any issues that arise to the necessary senior stakeholders within the business. There will also be some work with regards to customer returns/complaints, engineering change requests, and CAPAs.

Essential Requirements:

Previous experience as a Quality Assurance Engineer or similar
At least 3 years' experience conducting internal audits in line with ISO:13485 (Medical)

Desirable Requirements:

EUMDR and/or MDSAP
Experience with Engineering Change Requests
Experience with CAPAs
Understanding of UDI and GTIN

This is a fantastic opportunity for a Quality Assurance Engineer to work for a growing company who are working with some of the most advanced technology available. With the ambitious, but realistic plans the company has forecast there will be lots of opportunities to develop and progress internally if this appeals.

This is an immediate requirement so if you have the required skills and experience then please get in touch with an updated copy of your CV. Either apply direct or contact Adam on (phone number removed).

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