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Validation specialist

Perth
Brunel International
Posted: 7 May
Offer description

What are you going to do

Reporting to the Production Manager, the Validation Specialist will be responsible for driving validation programs across process validation, equipment qualification, and regulatory documentation. You will work closely with the Quality and Production teams to maintain strict GMP compliance across extraction, processing, and packaging operations.

Key Responsibilities:
* Develop, implement, and oversee validation protocols for process, equipment, and cleaning validation.
* Ensure full GMP compliance across extraction, processing, and packaging functions.
* Collaborate closely with Production and Quality teams to maintain regulatory standards.
* Prepare, review, and approve validation documentation and schedules for review.
* Work with QA/QC teams to ensure timely testing and validation reporting.
* Identify and implement corrective actions to maintain compliance.
Essential skills and knowledge
* Proven experience in validation roles within GMP-regulated industries (cannabis, pharmaceuticals, or similar).
* Strong understanding of equipment qualification, process validation, and regulatory documentation.
* Ability to work collaboratively with Quality, Production, and Regulatory teams.
* Strong attention to detail and a proactive approach to compliance and process improvements.
* Relevant qualifications in science, pharmaceutical, or engineering disciplines.
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