Quality Assurance Associate

Y-Axis; Sydney; Hybrid; AUD 60,000 - 90,000; Full time

Job summary

Care Essentials is seeking a Quality Assurance Associate to join our team for immediate start. This full-time remote role involves hands-on QA work aligned with GMP, regulatory, and customer requirements across QA/QC, production, warehouse, and management.

The candidate must manage quality actions through to completion, maintain controlled documents, review GMP records, and support audits and change controls in a fast-paced pharma environment.

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

Skills

Biotechnology

Job description

Quality Assurance Associate at Care Essentials

Full Time

Start Date

Immediate

Expiry Date

23 Nov, 26

0.0

Posted On

25 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Biotechnology

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