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. Solid attention to detail and teamwork are essential.