2mo ago , from Evolve Scientific Recruitment
About company/role:
Major pharmaceutical company
Based in the Northern suburbs
3-month casual contract, fulltime hours
Onsite position
Immediate start
Duties/responsibilities:
Provide real‐time review and approval of GMP records during manufacturing, QC, or warehouse operations.
Review and validation of protocols
Quality and validation related documentation review
Use MES, SAP, VEEVA, 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
Demonstratedexperience in aQA or Validation role within a GMP environment
Prior experience in technical writing, document review and stakeholder engagement




Excellent written and verbal communication skills
High attention to detail
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 andManufacturingsectors 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 advantages packages and accommodation, ensuring they are safely and compliantly able to support our clients.
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📌 Qa/Validation Associate (Melbourne)
🏢 Evolve Scientific
📍 Melbourne