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Execute activities related to manufacturing process transfer. Perform upstream production operations for lentiviral vectors and prepare associated production records and documentation. Establishment of cell banks for viral vector packaging. Routine maintenance of GMP production facilities. Manage the procurement and inventory of production materials. Assisting the PD team with relevant process development work as needed. Other tasks assigned by supervisors according to project requirements. Bachelor’s degree or above in pharmaceutical or biological sciences, or a related discipline. At least 2 years of hands-on GMP upstream production experience with viral vectors; familiar with GMP manufacturing workflows such as cleanroom gowning, material transfer, and room clearance procedures; strong awareness of aseptic operations. Candid...
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