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Charles River Laboratories

Quality Auditor/Compliance Specialist

Charles River Laboratories

  • Mayo
  • Negotiable
  • Permanent full-time
  • Updated 11/12/2012
  • HR Manager
this job is expired
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Quality Auditor required for busy CRO in the West of Ireland.


Charles River Laboratories is a world leader in contract research servicing the Pharmaceutical, Medical Device and Veterinary Industry. With more than 7,500 employees world-wide, we operate in 16 countries.

The Irish facility based in Co. Mayo is currently seeking to recruit an experienced Quality Auditor/Compliance Specialist to become part of the team in the Quality Department.

The main duties of this role are:

  1. Perform audits of technical transfer projects.
  2. Perform audits of facility/equipment validation projects
  3. Perform general auditing for compliance with quality standards.
  4. Prepare written reports on audit and inspection activities.
  5. Review SOPs.
  6. Assist in the administration of the Quality Department and of Quality systems.
  7. Assist with Vendor Assessment, client audits and subcontractor audits.

The successful candidate must have:

  • A degree in a relevant science discipline.
  • Experience of auditing validation projects.
  • Experience of working in a GLP/GMP environment preferable within the CRO or Pharmaceutical Industry.
  • 5 years + experience in a quality environment.


Ref: 12-15
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Charles River Laboratories

Charles River Laboratories


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