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 current 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 To be successful in this role, you will have: 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 Solid 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 Apply Now If you're looking to build your career in pharmaceutical validation and work on exciting equipment and systems projects, we'd love to hear from you.
Please submit your resume and cover letter in Word format.
Questions?
Contact Raine on (************* With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil Gas, Power Renewables, Chemicals, Construction Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide.
With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed.
We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading perks packages and accommodation, ensuring they are safely and compliantly able to support our clients.

📌 Validation Officer (Queensland)
🏢 Evolve Scientific
📍 Queensland