Job Description

About company/role:

  • Major pharmaceutical company
  • Based in the Northern suburbs
  • 4-month casual contract, fulltime hours
  • Hybrid position (3-4 days onsite)
  • Immediate start

Duties/responsibilities:

  • Provide real‑time review and approval of eGMP records during manufacturing, QC, or warehouse operations.
  • Review and validation of protocols
  • Quality and validation related documentation review
  • Use MES, SAP, VIVA, Microsoft Word, Excel, and other QA systems daily.
  • Contribute to updates and development of SOPs, protocols, and other GMP documents.
  • Apply root‑cause analysis and risk‑based decision‑making.
  • Liaise effectively with operations and other stakeholder departments.

Skills/experience:

  • Bachelor of Science or Engineering
  • Must have prior experience in a QA or Validation
  • Prior experience in te...

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