About the role

This is a hands-on quality role working closely with QA, QC, Production, Warehouse, and Management.

The successful candidate will support the ongoing operation of PharmAust’s Pharmaceutical Quality System and help ensure our products, processes, and documentation comply with GMP, regulatory, and customer requirements.

You must be organised, confident working with detailed technical documentation, and able to manage quality actions through to completion.

Key responsibilities

• Support the day-to-day operation of PharmAust’s Pharmaceutical Quality System
• Create, review, issue, maintain, and archive controlled documents
• Review batch manufacturing and packaging records for completeness and GMP compliance
• Assist with deviations, CAPAs, change controls, investigations, and product complaints
• Maintain QA registers, logs, training records, and quality-system trackers
• Prepare and review SOPs, specifications, forms, and quality records
• Follow up outstanding quality actions with relevant departments
• Assist with internal audits, customer audits, supplier audits, and regulatory inspections
• Support validation, qualification, and new-product introduction activities
• Assist with supplier and material qualification processes
• Contribute to product quality reviews and quality-data collation
• Promote GMP compliance and good documentation practices throughout the business
• Work collaboratively with Production, QC, Warehouse, and Management to resolve quality matters
• Essential experience and qualifications