Seek is seeking a Senior QA Associate in Sydney to lead validation activities and manage quality documentation within a GMP environment.
The role focuses on validation master plans, IQ/OQ/PQ, CSV, and relationship with production and technical teams.
The successful candidate will draft and maintain SOPs, ensure regulatory alignment with TGA GMP/PIC/S guidelines, support audits, and contribute to a robust QMS.
Robust attention to detail and teamwork are essential.
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📌 Senior Qa Associate: Validation & Documentation Lead (New South Wales)
🏢 seek.com.au
📍 New South Wales
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