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 technical writing, document review and stakeholder engagement
• Excellent written and verbal commuinication skills
• High attention to detail

Apply!
If you think this could be the role for you then please apply now! Please send us a cover letter AND a detailed resume in WORD format (PDFs can be corrupted / not processed).  
Or, if you have any questions, please contact Linda on 03 9040 1630.

With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.