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...