In this role, you will play a pivotal role in planning, executing, and documenting laboratory-scale downstream purification unit operations and drug substance intermediate (DSI) hold and stability studies. You will be directly responsible for the operational management of critical stability programs, including aseptic aliquoting, temperature-controlled sample logistics, sample accessioning, coordination with testing laboratories, and inventory management. You will work closely with senior scientists and engineers across the department and cross-functional teams to qualify purification processes, troubleshoot technical deviations, and deliver high-integrity datasets that safeguard commercial supply.
Key Skills Required:
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