Quality Assurance Associate

About the Role

We’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 Responsibilities

• Review and approve product batches, including validation of new products
• Act as an Authorised Person for batch release
• Analyse and report on environmental monitoring data
• Review GMP documentation, facility logs, and schedules
• Investigate and manage quality events and deviations
• Contribute to audits, inspections, and self-assessments
• Communicate with customers and support documentation development

About You

Additional Requirements

How to apply

Click 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 1987. We are here to engineer better Mondays. We love connecting talented people with great work opportunities in workplaces where you can thrive and make a meaningful difference. Apply For Job

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