Job Description

About the role:

  • Pharmaceutical organisation 
  • Based in the Southeast suburbs of Melbourne 
  • 12-months contract
  • Monday to Friday, full time hours

About your duties: 

  • Ensure manufacturing processes are meeting specifications
  • Develop and review validation protocols and reports for equipment, utilities and processes
  • Providing oversight of the sites quality systems and compliance
  • Perform real time review of records concurrent with manufacturing, QC, or warehouse operations on the floor
  • Utilise knowledge of root cause analysis and risk-based decision-making 
  • Support the development, revision and implementation of SOPs, protocols, and other GMP documents
  • Provide quality approval of deviations and CAPA as required
  • Conduct internal audits to verify adherence to quality systems and support external regulatory inspections

About yo...

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