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.

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

About the Prospect:

Reporting to the Associate Director, 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 teams to ensure improvements in compliance for CAPA's.
- Work collaboratively across functions to ensure metrics are met.
- 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 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 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.

📌 QA Associate (Melbourne)
🏢 Bell People Consultants
📍 Melbourne