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.
About the Opportunity
Reporting to the Quality Manager, key duties include the following:
Support manufacturing operations for document review, change controls & validation.
Ensure all manufacturing is completed to GMP standards.
Support review of deviations, quality review, CAPA's & change controls ensuring documents meet GMP quality standards.
Review validation protocols and engage with stakeholders for quality review of reports and documents.
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 knowledge of QA, CAPA's, deviations, change controls & deviations within pharmaceutical manufacturing.
Sound experience in Pharmaceutical/Medical Device Manufacturing or highly regulated environment.
Strong GMP knowledge.
Excellent Attention to detail & solid organisational skills.
Ability to work with wide range of stakeholders.
Culture & Benefits
This is an Excellent Contract Chance for a Quality Assurance Associate to join a leading global pharmaceutical organisation to support manufacturing operations, drive change controls & deviations for a major project.
Additional information
Global Pharmaceutical Manufacturer
Excellent Contract Prospect - START ASAP
Melbourne Metro Area
J-18808-Ljbffr
📌 Quality Assurance Associate Melbourne (Australia)
🏢 Bell People Consultants
📍 Australia
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