GMP Lab Quality Associate - Sample & Stability

HR Partners; Melbourne; On-site; AUD 65,000 - 85,000; Full time

Job summary

Randstad is assisting a global pharma/biotech leader in Australia to fill multiple Quality Control Associate roles within Sample Management and Lab Support in Melbourne. The position is 100% onsite at the Clayton facility, with morning and afternoon shifts, supporting GMP manufacturing operations and lab documentation workflows.

You will perform routine sample handling, LIMS-based tracking, stability coordination, and cross-functional collaboration to maintain data integrity and compliant

Qualifications

• Bachelor’s degree in a relevant scientific field.
• 2+ years of experience in a cGMP laboratory environment preferred.

Responsibilities

• Perform routine sample receipt, inspection, aliquoting, storage and shipment per GMP procedures.
• Prepare samples in biosafety cabinets using aseptic technique.
• Maintain complete traceability and chain of custody in LIMS.
• Coordinate stability sample pulls per study schedules and required timelines.
• Set up stability studies in LIMS and manage associated data.
• Monitor controlled‑temperature units and respond to alarms.
• Manage laboratory inventory and reagents to ensure uninterrupted operations.
• Support glassware washing, lab organisation and equipment maintenance.
• Ensure all work complies with cGMP, GDP, data integrity and safety requirements.
• Collaborate with QC, Manufacturing and cross‑functional teams to improve processes.

Skills

Quality Control

Sample Management

Documentation & Data Integrity

Team Collaboration

Education

Bachelor’s degree in a scientific discipline

Tools

LIMS

Job description

Randstad is assisting a global pharma/biotech leader in Australia to fill multiple Quality Control Associate roles within Sample Management and Lab Support in Melbourne. The position is 100% onsite at the Clayton facility, with morning and afternoon shifts, supporting GMP manufacturing operations and lab documentation workflows.

You will perform routine sample handling, LIMS-based tracking, stability coordination, and cross-functional collaboration to maintain data integrity and compliant