Mayne Pharma is seeking a documentation and quality systems qualified to join our fast-paced, regulated manufacturing site in Adelaide.
You will help ensure GMP-compliant documentation, SOPs and Master Batch Records remain accurate, current and audit-ready.
Working with Production, QA and SMEs, you'll drive continuous improvement across document control, investigations and CAPAs, supporting regulatory compliance and site quality outcomes.
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📌 Quality Documentation Specialist (Gmp & Compliance) (South Australia)
🏢 Mayne Pharma
📍 South Australia
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