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QA Auditor

Competitive + Benefits | Oxfordshire |  QA |  Permanent  | Ref:888051



Nadya Libecans

Which team do you work in? 

Drug Development

Which area do you specialise in?

Quality Control and Assurance

How do you keep up-to-date with the latest news in your sector?

I frequently read articles on changes and happenings in the industry, stay well connected on LinkedIn and regularly check in with relevant industry professionals.

What's your favourite film and why?

Honestly, I watch so many films it's difficult to pick just one, so for today I'm going to go with Mermaids because you can't go wrong with Cher!

If you could invent one thing what would it be?

Definitely would have to be heels that turn into flats so that I wouldn't have to carry two pairs of shoes everywhere anymore

What makes you #DistinctlyDifferent?

I believe knowledge is power and I strive to learn as much about people and the industry as possible to build lasting relationships and produce the best results for candidates and clients. 


The Role

QA Auditor - Global CRO - Oxford - £Competitive benefits


The Company

Our client is a global, leading and innovative CRO with a proven track record of a 90% on time enrolment of medication

  • Conduct studies for a range of therapies including Hemotology, Oncology, Infectious and Rare Diseases.

  • Are highly invested in their staff and highly encourage progression and promotions from within


The Role

Our company is looking for a highly skilled and engaging Quality Assurance Auditor to join their team in Oxford

  • Prepare, conduct and report on QA study audits

  • Compiling QA audit documentation

  • Train Operational staff in Quality Management topics

  • Prepare and conduct audits for internal systems, location and vendor qualification

  • Engage and communicate with auditees



  • University degree in Life Sciences or equivalent

  • Experience in QA or Quality Management in a Clinical Trials environment is essential

  • Ability to plan, conduct and report on QA audits without supervision

  • Exemplary working knowledge of GCP guidelines, EMA and FDA regulations is a must

  • Proficient in MS Office package, organisation, presentation and time management

  • Ability to travel locally and internationally


What should you do next?

This QA Auditor role is one not to be missed; it encompasses the opportunity to progress in an innovative and successful company. To discuss further, please submit your current CV or get in touch today.

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there.Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

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