Associate Director, Biologics Analytical
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About The Position
The Associate Director manages QC activities and external analytical development across multiple CMC biologics areas to support the development and manufacturing of biological drug candidates. The incumbent utilizes their technical expertise in clinical QC and analytical development such as batch release testing, stability management, method development, laboratory deviation investigation, and change control to advance CMC development and manufacturing for pre-IND and in-clinic biological molecules. Strong ownership is critical to ensure the speed, cost-effectiveness, and technical quality of our CMC activities. The individual works independently and in cross-functional teams and works effectively with third-party CDMOs and partners.
