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 secure 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.
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.
At Randstad, we are passionate about providing equal employment opportunities and embracing diversity to the benefit of all. We actively encourage applications from any background.
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📌 Analytical Method Validation Consultant (Brisbane)
🏢 Randstad
📍 Brisbane