Works cross functionally to identify, manage and implement site improvement projects utilizing Lean Six Sigma tools to drive optimal performance and reduce waste within the current Manufacturing Practice (cGMP) production and testing process environments. They will devise efficient ways to leverage our staff, equipment, materials and other resources in the manufacturing, testing, and supply chain of our biologic products. While this role is an independent contributor, they must cross functionally work and collaborate with Manufacturing, Laboratory Testing, Validation, Supply Chain, Facilities, and the Quality Assurance groups to optimize processes within the cell and gene therapies, monoclonal antibodies, and other biological processes.
A focus area for this position is Process Development, Technical Development and Analytical Development departments. Experience with continuous improvement in technical groups is a plus.
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Equal Opportunity Employer Minorities/Women/Veterans/Disabled