About the role:
* Pharmaceutical organisation
* Based in the Southeast suburbs of Melbourne
* 6‐month 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 site's 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:
* Tertiary education in Science, Engineering or Pharmaceutical Science
* Proven experience in QA and Validation to support qualification activities for manufacturing
* Must have 2 years experience in sterile manufacturing environments in a similar role
* Problem solving, creative thinking, and effective decision‐making skills
* Excellent communication skills, detail oriented and team collaboration
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