About the Role
Our client, a leading pharmaceutical manufacturer, is seeking an experienced IT Automation Specialist to support the implementation, maintenance, and continuous improvement of critical automated and computerised systems within a GMP-regulated setting. Working closely with Manufacturing, Engineering, Quality, and IT teams, you will play a key role in ensuring operational systems remain reliable, secure, compliant, and fit for purpose.
Key Responsibilities
Support the lifecycle management of automated and computerised systems across manufacturing operations
Implement, configure, maintain, and enhance manufacturing and operational technology systems
Support system upgrades, integrations, migrations, and technology improvement projects
Develop and maintain technical and compliance-related documentation
Assist with system testing, troubleshooting, investigations, and issue resolution
Support data integrity, cybersecurity, and compliance initiatives
Partner with Quality, Engineering, Manufacturing, and IT stakeholders to deliver system improvements
Contribute to continuous improvement initiatives focused on system performance, reliability, and efficiency
Ensure activities are performed in accordance with GMP, company policies, and health and safety requirements
Skills & Experience
Bachelor's degree in Information Technology, Engineering,



Automation, Computer Science, or a related scientific discipline
3-5+ years' experience in an IT, Automation, Engineering, Manufacturing Systems, or Operational Technology role
Experience working within a regulated environment such as pharmaceuticals, biotechnology, medical devices, or other compliance-driven industries
Hands-on experience supporting or implementing manufacturing, automation, or computerised systems
Experience with systems such as MES, SCADA, PLC, Historian, LIMS, ERP, or similar platforms is highly desirable
Experience delivering system upgrades, implementations, integrations, or technology projects
Exposure to system validation, lifecycle documentation, testing, or data integrity activities will be highly regarded
Knowledge of GMP environments, GAMP 5, FDA 21 CFR Part 11, or PIC/S requirements will be viewed favourably
Strong technical troubleshooting, stakeholder management, and problem-solving skills
Additional Information
Successful candidates will be required to complete a pre-employment medical assessment. Please note this site is not accessible via public transport, and applicants must have reliable private transport to travel to and from the site.
Questions? Contact Raine on **************
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📌 It Automation Specialist (Queensland)
🏢 Evolve Scientific
📍 Queensland