About the Role
Our client, a leading pharmaceutical manufacturer based in Brisbane's western suburbs, is seeking a
Validation Officer
to support their
Quality Assurance team
on a casual contract through to the end of ****.
This role will play a key part in supporting equipment and system validation activities across the site. Working closely with QA, laboratory teams, engineering and external vendors, you will assist with the qualification of new equipment, coordination of validation activities, and execution of validation protocols to ensure compliance with GMP and regulatory requirements.
This is an excellent opportunity for someone with a pharmaceutical QA, QC or validation background looking to further develop their experience within validation and quality systems.
Please note:
The site is not accessible via public transport; therefore, reliable private transport is essential.
Key Responsibilities
Coordinate validation activities for new equipment and system implementation projects
Liaise with vendors and internal stakeholders to manage installation schedules and validation timelines
Execute and document Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities
Support Computer System Validation (CSV) activities for new and existing laboratory systems
Prepare, review, and maintain validation protocols, reports, and associated documentation
Assist with equipment and system assessments, upgrades,



and lifecycle management activities
Support implementation of new laboratory equipment and technologies
Ensure all validation activities are performed in accordance with GMP requirements and company procedures
Assist with investigations, deviations, CAPAs, and change controls where required
Maintain accurate, compliant, and audit-ready documentation
Contribute to continuous improvement initiatives across laboratory and validation processes
Skills & Experience
A degree in Science, Chemistry, Pharmaceutical Science, Biomedical Science, or a related discipline
Previous experience within a pharmaceutical, biotechnology, medical device, or other GMP-regulated environment
Experience working in a QC laboratory, QA, validation, laboratory support, or technical role
Exposure to equipment qualification and validation activities, including IQ/OQ/PQ execution
Understanding of GMP requirements and Good Documentation Practices
Exposure to Computer System Validation (CSV) or laboratory computerised systems would be highly regarded
Experience with laboratory instrumentation, calibration, maintenance, or troubleshooting would be advantageous
Robust written documentation and technical reporting skills
Excellent organisational and stakeholder management abilities
A proactive approach with the ability to manage multiple priorities in a fast-paced environment
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📌 Validation Officer (Queensland)
🏢 Evolve Scientific
📍 Queensland