Job Description
About the Company
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Operating as a global pharmaceutical manufacturer, 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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About the Opportunity
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Reporting to the Quality Manager, key duties include the following:
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Support manufacturing operations for document review, change controls & validation.
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Ensure all manufacturing is completed to GMP standards.
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Support review of deviations, quality review, CAPA's & change controls ensuring documents meet GMP quality standards.
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Review validation protocols and engage with stakeholders for quality review of reports and documents.
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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 knowledge of QA, CAPA's, deviations, change controls & deviations within pharmaceutical manufacturing.
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Sound experience in Pharmaceutical/Medical Device Manufacturing or highly regulated environment.
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Strong GMP knowledge.
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Excellent Attention to detail & strong 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 Contract Prospect for a Quality Assurance Associate to join a leading global pharmaceutical organisation to support manufacturing operations, drive change controls & deviations for a major project.
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Additional information
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Global Pharmaceutical Manufacturer
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Excellent Contract Opportunity - START ASAP
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Melbourne Metro Area
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#J-*****-Ljbffr

📌 Quality Assurance Associate (Victoria)
🏢 Bell People Consultants
📍 Victoria