QA Manufacturing Associate

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.

Due to increase in project requirements, an opportunity has now arisen for a Manufacturing QA Associate to provide QA support in deviations, change controls & CAPA's across manufacturing, engineering & quality.

About the Opportunity:

Reporting to the Quality Manager, key duties include the following:

• Lead investigations & write up deviations, complete & write CAPA's & change controls to regulatory guidelines.
• Review quality documents, change controls & quality compliance work.
• Provide & represent QA in GMP manufacturing operations.
• Work with manufacturing teams to ensure improvements in compliance for CAPA's.
• Work collaboratively across functions in quality, engineering & manufacturing to ensure metrics are met.
• Effectively liaise with internal & external key stakeholders.

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 environment.
• 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 & Benefits:

This is an Excellent Contract Opportunity for a Manufacturing QA Associate to join a leading global pharmaceutical organisation to support manufacturing operations, drive change controls & deviations for a major project.

How To Apply

To Apply for this role, please click the APPLY NOW button.

For a confidential discussion, please contact Sue Campbell on 0417 994 917.

NB - Only Shortlisted candidates will be contacted.