Opportunity Description
Primary Responsibilities:
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<li>Lead scientific strategy for drug substance development, ensuring scalable, efficient, and compliant processes that meet clinical and commercial needs</li>
<li>Oversee contract service providers (CSPs) to develop, optimize, and scale manufacturing processes from preclinical through commercialization</li>
<li>Apply risk assessments and Quality by Design (QbD) principles to define design space and establish robust control strategies</li>
<li>Develop end-to-end drug substance strategies supporting product quality, global regulatory approvals, and supply chain flexibility</li>
<li>Manage technology transfer, outsourcing, and external manufacturing to build a reliable and scalable supply chain</li>
<li>Establish, evaluate, and manage CSP partnerships, including contract negotiation, performance oversight, and issue resolu...
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