About the role:

• Pharmaceutical organisation 
• Based in the Southeast suburbs of Melbourne 
• 6-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 you...