This role will sit within the CMC Analytical Sciences organization and will partner closely with Analytical, MSAT, Quality, Regulatory Affairs, Supply Chain, and external CDMOs/CROs to ensure that analytical strategies, statistical approaches, and data packages are scientifically robust, phase-appropriate, compliant, and suitable for global regulatory submissions and commercial readiness. The Associate Director of Analytical Development and CMC Statistics will provide technical and statistical leadership for analytical development, method validation, method transfer, comparability, stability, specifications, and lifecycle management activities supporting biologic drug substance and drug product programs.