Dissolution Analytical Development Lead

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as the Dissolution Analytical Development Lead based in Cambridge, MA reporting to the Head, AD Synthetic Molecule. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to work towards their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, and work toward excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to provide Better Health and a Brighter Future to people around the world. Here, you will be a necessary contributor to our inspiring, bold mission. GOALS: Lead rationale dissolution method development and platform technology establishment across multiple programs , enabling phase appropriate method development , qualification , tech-tran s fer, biopharmaceutics assessment and robust comparability . Establish the dissolution strategies ( both in regulatory and technical aspects ) as a center of excellence to accelerate clinical development and mitigate the risks together with formulation team . Partner with senior stakeholders (Fo rmulation development , process development , R&D quality and regulatory affair ) to align the quality control and regu l atory strategy throughout early to late stage development . A CCOUNTABILITIES : Analytical Development: Lead dissolution method development , qualification and tech-transfer across the programs to ensure the reliable product quality, stability and consistent performance in clinical development. Dissolution Strategy Establishment : S trategically develop and implement dissolution testing from both regulatory and technical perspectives to serve as a guide for formulation and clinical development, contributing to the acceleration of clinical development. Platform Technology Development : Collaborate with process analytics and characterization teams , lead the implementation of automated dissolution system and biorelevant dissolution assessment to establish globally harmonized approach. Roadmaps and Cross-functional Collaboration: Lead strategy and multi-year roadmaps fo r capability expansion in dissolution technologies and align priorities across stakeholders; manage risks and value realization; and drive continuous improvement and innovation. Lead the Dissolution Analytics Development team to deliver precise, robust and reproducible dissolution methods and meaningful specification setting across the programs. Build the end-to-end control strategies related dissolution using A QbD principles, ensuring scientific rigor and phase-appropriate bridging to GMP release and stability methods. Establish the automat ed dissolutio