The Director Quality Operations will be responsible for partnering with functional stakeholders at the site level to ensure Quality performance and Compliance is designed into, and maintained, across all strategic initiatives, Operations, functional support organizations, and execution of GMP activities at the Memphis site. The Director of Quality Operations is responsible to oversee execution and delivery from the following areas of the organization: Drug Product Disposition, Functional Organization Quality Oversight, On The Floor Quality, Raw Material Testing and Release as well as customer facing Quality program leads for each client in the CDMO- Memphis portfolio. The person filling this role will be responsible for the leadership, development and training of team members within their oversight as well as providing supportive leadership and strategic direction to operate with and maintain compliance to regulatory and industry quality standards in support of existing and new cellular therapy production.