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We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs…
Oversee R&D quality audits, inspections, CAPA management, and regulatory compliance for cancer therapies in APAC, ensuring GxP standards and PMDA/NMPA alignment.
Lead end-to-end supply chain planning for cell & gene therapies, coordinating manufacturing, viral vectors, and logistics to ensure reliable patient delivery and portfolio growth.
Oversee early-phase clinical trials for antiviral therapies, managing budgets, timelines, and cross-functional teams to ensure regulatory compliance and high-quality data for drug development.
Designs and leads a global trade compliance program ensuring adherence to international import/export laws across Gilead's pharmaceutical supply chain. Partners with Legal, Tax, and Finance on regulatory compliance, customs, risk management, and systems like SAP GTS.
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve…
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