Nurix seeks a PhD-level specialist to lead cGMP manufacturing of drug substances, from scale-up through commercialization. You will oversee CMOs, drive QbD studies, and ensure regulatory-compliant CMC submissions, interacting with US/EU authorities as needed.
The role requires expertise in IND/CMC regulatory filings, process characterization, and robust DS control strategies, with up to 50% travel.
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📌 Associate Director, Drug Substance Cmc & Process Development (Brisbane)
🏢 Nurix
📍 Brisbane
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