2mo ago , from Evolve Scientific RecruitmentAbout company/role:Major pharmaceutical companyBased in the Northern suburbs3-month casual contract, fulltime hoursOnsite positionImmediate startDuties/responsibilities:Provide real‐time review and approval of GMP records during manufacturing, QC, or warehouse operations.Review and validation of protocolsQuality and validation related documentation reviewUse 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 EngineeringDemonstratedexperience in aQA or Validation role within a GMP environmentPrior experience in technical writing,



document review and stakeholder engagementExcellent written and verbal communication skillsHigh attention to detailWith 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 perks packages and accommodation, ensuring they are safely and compliantly able to support our clients.
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📌 Qa/Validation Associate (Victoria)
🏢 Evolve Scientific
📍 Victoria