Our client, a leading pharmaceutical manufacturing company known for its commitment to innovation and quality, is seeking an Analytical Method Validation Consultant to join their dedicated laboratory team in the northern suburbs of Brisbane. This is a Casual Position with Full-Time Hours (Monday to Friday), offering a stable role in a high-quality environment.

The Role We are seeking a hands-on Analytical Method Validation Consultant to support critical raw material testing within a high-quality GMP QC laboratory environment. This is a critical role that combines practical analytical execution with the authoring of audit-ready validation and verification documentation. You will be instrumental in troubleshooting methods and ensuring the robust implementation of both compendial (USP/BP/Ph. Eur.) and non-compendial methods for complex raw materials.Key Responsibilities

• Execute hands-on method validation/verification for raw materials in the laboratory.
• Author, review, and remediate all controlled validation documentation (plans, protocols, and reports) to be audit-ready.
• Troubleshoot analytical methods, instrumentation, and sample preparation issues.
• Collaborate closely with QC and QA teams to ensure compliance and data integrity across all testing.
• Provide knowledge transfer and training to QC analysts.

Required Experience (Must-Have)

• Strong hands-on analytical method validation/verification experience in a GMP QC laboratory.
• Proven ability to write and defend regulated validation documentation (plans, protocols, reports).
• Expertise in common pharmaceutical analytical techniques, including HPLC/UPLC, FTIR, GC, Wet Chemistry, and UV-Vis.
• Exceptional data integrity and documentation discipline.

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