Lead & develop a team of scientists in Analytical Controls/Compliance-Global CMC program oversight of Pharmaceutical Sciences (PS) with managementand oversight of all local project-related analytical control topics, developmentrequirements and program milestones including global reporting-Oversee and manage core tasks for Analytical Controls for clinical trial materialefforts across four main areas: a) GMP review and control for analytical documents b)Release testing oversight, Stability and Shelf life c) Reference Standard Management d) GMP Quality Systems-Contribute to product development and product quality oversight by collaborating with multiple functions within Pharmaceutical Science-Contribute to the overall functional direction globally and represent function withinCMC/Pharmaceutical Science and across the global Takeda organization.

Member of the Analytical Development group, with a focus on gene therapy products.

Member of the Bioanalytical Development Group

Involved in a Phase I Clinical Trial utilizing genetically engineered T Cells as a form of Adoptive Immunotherapy.