Job Description

About the company/role:

  • Major pharmaceutical company
  • Based in Northern suburbs
  • 2-month casual contract
  • Full-time hours, Mon-Fri
  • ASAP start

Your responsibilities include, but not limited to:

  • Lead and close out deviation investigations, ensuring accurate documentation and timely QA approval
  • Collaborate with manufacturing and QA teams to assess deviation scope, root causes, and required CAPAs
  • Coordinate process and operational changes, engaging SMEs and ensuring tasks progress to completion
  • Act as change coordinator for GxP changes and support cross‑functional project teams
  • Support daily operational meetings, providing updates and troubleshooting operational issues
  • Prepare and update documentation, including FMEAs and risk assessments
  • Monitor progress of deviations and changes, escalating risks to timelines when needed

S...

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