About the Role

Our client, a leading pharmaceutical manufacturing company based in Brisbane's western suburbs, is seeking an experienced Validation Engineer to join their team on a casual ongoing basis for 6-12 months, working Monday to Friday, 38 hours per week.

This role will support validation and qualification activities across maintenance/Engineering, Production and Packaging, providing technical expertise for equipment, facilities and systems within a GMP-regulated manufacturing setting.

Please note: Applicants will be required to successfully complete a medical assessment, drug screening and police check.

Key Responsibilities

- Execute equipment, facility and system validation and qualification activities.
- Develop and execute validation documentation, including URS, FS, Risk Assessments, IQ, OQ, PQ and validation reports.
- Support new equipment/system installations, upgrades and lifecycle management.




- Provide technical support for equipment changes and risk-based change management.
- Investigate and report deviations and support Continuous Improvement initiatives.
- Ensure activities comply with GMP/cGMP, company procedures and health and safety requirements.

Skills & Experience

- A Bachelor's degree in Engineering, Science or a related discipline.
- Hands-on experience with equipment, facility and/or system validation and qualification.
- Experience with validation lifecycle documentation such as URS, FS, DS, IQ, OQ, PQ and Traceability Matrices.
- Experience working in a GMP manufacturing or highly regulated environment.
- Understanding of risk-based change management/change control.
- Strong technical writing, communication and organisational skills.
- Experience in Manufacturing and working with Project Management Systems.

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📌 Pharmaceutical Validation Engineer (Ipswich)
🏢 Evolve Scientific
📍 Ipswich