About the Company

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 & robust organisational skills.
- Ability to work with wide range of stakeholders.

Culture & Benefits

This is an Excellent Contract Opportunity 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 Opportunity - START ASAP
- Melbourne Metro Area

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