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Quality Compliance Engineer

AVD Appoint

Neath

On-site

GBP 42,000

Full time

23 days ago

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Job summary

Join a cutting-edge technology firm as a Quality Assurance Engineer in Glamorgan, where you will ensure compliance with ISO:13485 standards through internal audits. This role offers the chance to work with innovative products and contribute to the company's growth. With a strong focus on quality and customer satisfaction, you will manage audit processes and address engineering changes and CAPAs. This is an exciting opportunity to develop your career in a dynamic environment where your contributions will have a significant impact. If you're ready to take the next step, this role awaits you!

Qualifications

  • 3+ years of experience as a Quality Assurance Engineer or similar role.
  • Proficient in conducting internal audits per ISO:13485 standards.

Responsibilities

  • Conduct internal audits and manage the audit schedule.
  • Handle customer returns, complaints, and engineering change requests.

Skills

Quality Assurance
Internal Audits
ISO:13485
Engineering Change Requests
CAPAs

Job description

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:

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


Desirable Requirements:

  1. EUMDR and/or MDSAP
  2. Experience with Engineering Change Requests
  3. Experience with CAPAs
  4. 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 #removed#.

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