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Job Details
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QA Auditor

Business Type: Clinical Research Organisation
Job Type: Quality Assurance - Control
Job Level: Experienced (non manager)
Position: Full Time
Salary: £Competitive
Location: Hertfordshire
Reference: 889271
Closing Date: 05/11/19
Job Details:

QA Auditor - CRO - Hertfordshire - £Competitive

The Company

Our client is a highly reputable CRO that provide end to end support to the pharma, biotech and medical devices markets worldwide. They conduct clinical trials from Phases I - IV and specialise in drug development and commercialisation of products for their clients. They pride themselves on their long-term relationships, accountability for their products and provide an exceptional patient focused service.

The Role

They are looking for an experienced QA Auditor to join their team in Hertfordshire! Tis role is reporting to the VP of QA and would be working within a specialist Quality team. Responsibilities of the role include:

  • Ensure the annual risk assessment of activities undertaken by the company is conducted, that the audit schedule is updated quarterly and that the audit tracker is regularly maintained.
  • Ensure SOPs to support the audit function are maintained.
  • Promote and represent the companies'' auditing/due diligence or other QA related capabilities at business development/bid-defence meetings and assisting with proposal development for client projects involving audits, due diligence or other QA related activities.
  • Project manage audit/due diligence or other QA related service projects including account management for these projects (input into work order and invoice preparation) and resource management of external auditor/QA consultant.
  • Any other reasonable task as approved by your Line Manager
  • Commit to training and complete assigned training on time
  • Adhere to company SOPs and procedures; and dependent on project, to project specific procedures or Client SOPs and procedures, as appropriate


To apply for this role, you must have the following experience:

  • 5 years GCP auditing experience
  • GVP, GDP or GMP experience preferred but not mandatory
  • Education to graduate level in a science discipline, nursing or equivalent, or possession of substantial relevant experience in a Clinical Research/PVG or QA environment
  • Ability to travel occasionally for Auditing purposes
  • Ability to work individually and unsupervised

What should you do next?

This QA Auditing role is one not to be missed; it encompasses the opportunity to working for a highly reputable, global business. To discuss further, please submit your current CV.

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.

Posted: 08/10/2019 | NPJ Ref: 243145
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