QA Associate

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...