About the Company

Operating as a global pharmaceutical player, our client is well known for its growth and innovation offering a range of healthcare and pharmaceutical products to local & global markets.

An Opportunity has now arisen for a QA Associate to work closely with manufacturing operations for document review, change controls, CAPA's and validation operations.   

About the Opportunity

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

• Perform routine quality walkthroughs of the GMP facility operations.
• Provide support, review & approval of GMP documentation.
• Review quality documents, change control, CAPA's & quality compliance work.
• Review validation protocols. document review & validation.
• Engage with manufacturing to for quality problem solving.(
• Collaborate with cross functional teams & effectively liaise with all parties.  

About You

The successful candidate will have the following skills & experience:

• Tertiary qualifications in Science or Engineering.
• Sound experience in QA within a Pharmaceutical/Medical Device.
• Sound knowledge of QA, CAPA's & deviations and document review. 
• Strong GMP knowledge.
• Excellent Attention to detail & strong organisational skills.
• Well developed interpersonal & communication 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 04•• ••• 917.

NB - Only Shortlisted candidates will be contacted.