Cancel
Return to Job Search
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
Apply Now

Description

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
Apply Now
Report This Job

Charles River Laboratories

Charles River Laboratories

 

View Employer Profile

Show More

Email me jobs similar to: Quality Auditor/Compliance Specialist

Please enter your email address

Please enter a valid email address

We use cookies to customise our website for you, giving you the best possible user experience. If you continue without changing your settings, we’ll assume that you are happy to receive this personalisation. Find out more about our cookie policy

Accept & Close