About the Company
Operating as a global pharmaceutical player, our client is well known for its growth and innovation offering a range of healthcare and pharmaceutical products to local & global markets.
Due to increase in project requirements, an opportunity has now arisen for a QA Associate to provide support across all operations.
About the Opportunity
Reporting to the Quality Manager, key duties include the following:
Engage with manufacturing to ensure all documentation is to GMP standards.
Review quality documents, change control, CAPA's & quality compliance work.
Review validation protocols and document review of quality reports.
Work with teams to ensure improve compliance for CAPA's.
Effectively liaise with internal & external key stakeholders of the projects.
About You




The successful candidate will have the following skills & experience:
Tertiary qualifications in Science or Engineering.
Sound experience in Pharmaceutical/Medical Device Manufacturing or highly regulated setting.
Sound knowledge of QA, CAPA's & deviations within manufacturing.
Strong GMP knowledge.
Excellent Attention to detail & strong organisational skills.
Ability to work with wide range of stakeholders.
Culture & Advantages:
This is an Excellent Short Term Contract Opportunity for a QA Associateto join a leading global pharmaceutical organisation to support manufacturing operations, drive change controls & deviations for a major project.
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📌 Qa Associate (Melbourne)
🏢 Bell People Consultants
📍 Melbourne