GCP QA Auditor

  1. Permanent
London, England
  1. Quality Assurance, Auditing
Posted: 02/08/2023

This vacancy has now expired. Please see similar roles below...

Hobson Prior are looking for a GCP QA Auditor to join a CRO on a permanent basis located in London.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

  • For this role, you will plan, organize, and report internal and external audits.
  • Providing support to our audit schedule and esteemed clients.
  • Under the supervision of the QA Manager, you will be responsible for conducting GxP audits,
  • Identifying trends, identifying corrective actions, and categorizing observations.
  • As part of your duties, you'll support initiatives for business improvement with departmental heads.
  • Contribute to projects and assist with client audits.
  • Provide support and services for pharmaceutical and medical device clinical trials.


  • An undergraduate degree in a science subject is required.
  • A minimum of 4 years of prior experience auditing to GCP standards, preferably in pharmaceuticals/biotech.
  • An understanding of the compliance requirements for clinical trials is essential.
  • Hold a valid driver's license.
  • Ability to travel approximately 50 percent of the time.
  • Operate across Europe, North America, South America, Asia, Africa, and Australasia for audits.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

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