Job Details

Job Summary:

If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, French and German speaking candidates should call Marc Van de Voorde in our Swiss office, on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world call Mark Twigden, in the UK London office, on +44 (0)207 801 3383.

Requirements:

***Quality Assurance Auditors*** UK*** 1-3 years’ experience *** Great Career opportunity within exciting Clinical research Organisation. Accelerate your career with this great QA role.

Location: UK

Role: Quality Assurance Auditor
 

This is a great opportunity to join an expanding CRO organisation and gain valuable auditing experience.

As a successful QA auditor you will be responsible to perform GCP audits according to the QA organization’s standards and ensure that business activity and quality systems are in accordance with the company SOPs and local regulations. You will support the Corporate Review and perform customer audits, mock inspections and facility inspections where required.
 

This is a good entry-level role, in which the right person will be able to shine and make a name for themselves within a CRO company with a global reach. You should have a one to three years auditing experience and a sound knowledge of GCP and quality system regulations.
 

Take the next step with a provider of outsourced development services to pharma, biotechnology and medical device industries. My client is a proven strategic developer, bringing management and analysis in clinical development; from compound selection to phase I-IV clinical studies.
 

If you are interested in these roles, please call Mark Twigden on 0207 801 3383 or alternatively, you can email me at mt@advanced.com
 

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If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, French and German speaking candidates should call Marc Van de Voorde in our Swiss office, on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world call Mark Twigden, in the UK London office, on +44 (0)207 801 3383.
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About Advanced

 

Advanced Regulatory has been operating since 2004. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs, Quality Assurance, Clinical Development, Pharmacovigilance and Health Economics and Outcomes Research. We match professional candidates to the best permanent, contract and interim roles in the market.
Visit us at
www.advregulatory.com

 

Keywords Key Words: QA, Quality Assurance, GCP, GMP, GCP, GxP, Commercial, Product Development, Good Manufacturing Practice, Good Clinical Practice, SOP, Risk Management, Six Sigma, Monitoring, Regulatory, Compliance, CAPA, ISO