Quality Assurance Associate

About the RoleWe're seeking a motivated QA Associate to join their dedicated team in Mt Wellington supporting the manufacture of highly specialised pharmaceutical products.

In this critical role, you'll help ensure that Good Manufacturing Practice (GMP) is upheld throughout the production process — from batch review to documentation control and audit participation.

You'll have the opportunity to make a tangible impact on products that improve patient outcomes across Australia and New Zealand.

Full training will be provided.

You'll be working regular day shifts, Monday to Friday.Key ResponsibilitiesReview and approve product batches, including validation of new productsAct as an Authorised Person for batch releaseAnalyse and report on environmental monitoring dataReview GMP documentation, facility logs, and schedulesInvestigate and manage quality events and deviationsContribute to audits, inspections, and self-assessmentsCommunicate with customers and support documentation developmentAbout YouDegree-qualified in science or a related field (mandatory)Exceptional attention to detail, accuracy, and adherence to SOPsStrong communication and collaboration skillsOrganised, proactive, and able to work independentlyProficient with Microsoft Office (Word, Excel, PowerPoint)Previous pharmaceutical or GMP manufacturing experience (advantageous but not essential)Additional RequirementsCurrent driver's licenceFully vaccinated against COVID-19How to applyClick APPLY NOW, we look forward to seeing your CV!

Any questions can be emailed confidentially to

• or call
• To apply for this vacancy, you MUST be a NZ citizen or resident, or have already secured the right to work in NZ and therefore hold a valid visa.Scitex specialises in permanent, contract and temporary recruitment – and has done so since

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