Job Description

The role:

QA Cleaning Validation roles required for a multinational client based in Limerick


  • Taking Cleaning Validation samples alongside Upstream/Downstream processing.
  • Working closely with manufacturing to ensure the CIP/SIP and dirty holds are to the correct times and samples are taken.
  • Shows focus & a consistence approach to the role and tasks.
  • Execution of cleaning validation protocols.
  • Generating and Executing Validation Protocols.
  • Experience in continuing validation and generation of assessments for continuing
  • Actively look for Continuous improvements
  • An excellent understanding of how manufacturing/Cleaning
  • Validation/Cleaning equipment works and load configuration for small parts loads
  • Understanding of baseline studies for new equipment
  • Generate/review/Approval of CV protocols,
  • Generate Reports
  • Maintain and update Cleaning Validation Plan
  • Schedule of cleaning activities with Manufacturing
  • Liaise with numerous departments
  • Ensure Training is maintained and current.

Education and Experience:

  • Experienced in QA Validation activities –
  • Experience on writing and approving Deviations/ GMP documents
  • Technical writing experience in writing site reports.
  • Experience in Validation specifically cleaning validation
  • Experience in assessment of cleaning issues during study runs,
  • Experience in Deviation/Change control writing,
  • Experience in aseptic technique
  • Experience in Gowning for IOS7/ISO8

Add a Cover Note to your Application

Register to apply for this job and others using an online resume. Register
Upload your CV/Resume or any other relevant file.

Please answer employers questions below.


I agree to's Terms & Conditions

Get Updates - I would like to receive news and updates about jobs, opportunities and advice from