In this role, you will utilize strong working knowledge in immunology and/or cancer research and extensive hands-on experience to identify, validate and characterize novel immunological pathways and/or therapeutics.
In this role, the selected candidate will support the technical transfer process, investigations, and batch record generation for cGMP manufacturing and to partner with internal and external clients to design and support manufacturing processes.
In this role, the selected candidate will be responsible for the development and implementation of operation related strategies for the effective commercialization and Global launch of assets in the company Pipeline.
In this role, the selected candidate will perform facility fit evaluation, then technology transfer and scale up of Downstream protein manufacturing process in conjunction with the process development laboratory, client, manufacturing, and quality assurance.
In this role, the selected candidate will be responsible for general and specific assignments involving complex and novel types of plans, investigations, surveys, environmental impact assessment, major regulatory issues, permits, approvals, comments, and expert testimony preparation and presentation.