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Quality Assurance Administrator

Quality Assurance Administrator

  • Location

    Cardiff

  • Sector:

    Engineering & Technical

  • Job type:

    Permanent

  • Salary:

    £22,000 - £25,000 per annum plus benefits

  • Contact:

    Angharad Isaac

  • Email:

    aisaac@yolkrecruitment.com

  • Job ref:

    25229

  • Published:

    almost 3 years ago

  • Expiry date:

    2021-05-30

Quality Assurance Administrator

£22,000 - £25,000 per annum plus benefits

Cardiff

 

This leading global medical manufacturing business has established their first UK manufacturing facility in South Wales and has created a new opportunity for a Quality Assurance Administrator to join their growing team.

 

This is a rare opportunity for a QA Administrator to join an exciting business that has a strong record of consistent growth and investment. You will be offered a strong culture that will allow you to achieve your personal and professional goals. You'll need previous experience in a QA or QC role within medical, pharma, food or similarly regulated environment and will be able to make a difference in a growing business while receiving support from the senior team.

 

As Quality Assurance Administrator you’ll be

 

  • Create all necessary documentation for the quality processes
  • Administration of QA reviews for Production Batch Records
  • Administration of QA release for finished products
  • Co-ordinate change control and document management within the QMS.
  • Partner with and support operations to evaluate and address quality events including nonconformances, product dispositions, root cause investigations, and implement appropriate CAPA based on risk level.
  • Collation, analysis, and presentation of quality performance KPIs.
  • Support continuous improvement activities by seeking out opportunities to optimize processes and systems to reduce variation and improve product quality. 
  • Support with implementation of best practices to eliminate repeat quality events and improve product quality.
  • Support and participate in inspection readiness activities by developing or applying working knowledge of ISO13485 and 21CFR Part 820 regulations.


This is the experience you’ll bring to the team
 

  • Ideally 2-3 years of experience working in a Quality department in a highly regulated manufacturing environment (Diagnostics, Medical Device, Pharmaceutical, or Consumer).

 

And this is what you’ll get in return

 

  • A market leading salary
  • 36 days holidays (25 + 3 days at Christmas + bank holidays)
  • 5% employer contribution pension
  • Private health insurance
  • Outstanding leadership and support
  • Professional / career development opportunities

 

If you feel you have the skills, experience and passion to be successful in this role apply now.  

*Please note, whilst we do our best to contact all candidates, due to the high number of applications we receive we cannot guarantee this for every role. If you have not heard anything from us within 7 days of applying - then unfortunately you have been unsuccessful. Please keep an eye on our website for more opportunities.

 

 

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