Job Description
About the Company
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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.
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Due to increase in project requirements, an opportunity has now arisen for a QA Associate to provide support across all operations.
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About the Opportunity
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Reporting to the Quality Manager, key duties include the following:
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Engage with manufacturing to ensure all documentation is to GMP standards.
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Review quality documents, change control, CAPA's & quality compliance work.
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Review validation protocols and document review of quality reports.
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Work with teams to ensure improve compliance for CAPA's.
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Effectively liaise with internal & external key stakeholders of the projects.
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About You
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The successful candidate will have the following skills & experience:
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Tertiary qualifications in Science or Engineering.
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Sound experience in
Pharmaceutical/Medical
Device Manufacturing or highly regulated environment.
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Sound knowledge of QA, CAPA's & deviations within manufacturing.
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Strong GMP knowledge.
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Excellent Attention to detail & robust organisational skills.
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Ability to work with wide range of stakeholders.
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Culture & Benefits:
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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 (Victoria)
🏢 Bell People Consultants
📍 Victoria