Associate Director Supply chain - Biologics OpU

Location: Lexington
Posted on: June 23, 2025

Job Description:

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 ABOUT THE ROLE The Associate Director Supply chain - Biologics OpU is responsible for driving cross-functional projects across Takeda’s Biologics Supply Chain Operating Unit, encompassing both internal and external manufacturing sites. This role focuses on developing and aligning best practices, enhancing performance management systems, and enabling end-to-end supply chain visibility and control through innovative tools and standardized processes. It also plays a key role in supporting strategic decision-making through preparation of governance materials and contributing to the overall performance and sustainability of the global supply chain function. HOW YOU CONTRIBUTE Deliver high-impact Ad Hoc projects under the guidance of the Global Supply Chain Head. Design and implement systems to enhance visibility, predictability, and control of key operating parameters e.g. inventory, volume reporting, manufacturing and planning parameters, across the Operating Unit. Develop tools and processes to optimize the three core supply chain levers: inventory, lead time, and capacity. Measure, align, and improve manufacturing site capacity, collaborating closely with operations teams. Partner with Business Excellence teams and Global Manufacturing functions to drive improvements in processes aligned to global demand reviews and supply site utilization as well as operational effectiveness. Standardize master scheduling methodologies using APICS PSI formats to ensure end-to-end visibility. Build and foster a collaborative Supply Chain community across sites and global functions, focusing on alignment for budgeting cycles, capability development, and information sharing. Contribute to the creation and deployment of systems that support sustainable provisioning and regulatory change control integration. WHAT YOU BRING TO TAKEDA Bachelor’s degree with 5 years of experience in GMP Manufacturing, Supply Chain, or Operations (MSc or MBA preferred). APICS certification. Knowledge of regulatory change control processes in a global supply chain context. SAP IBP / OBP and APO PPDS experience Broad understanding of supply chain functions, including planning, logistics, inventory, MRP, procurement, and lean manufacturing. Demonstrated experience in managing and implementing change, in a global operating context, including digital transformation and AI-driven tools. Proven ability to lead cross-functional teams and operate effectively in matrixed, multicultural organizations. Strong analytical skills with the ability to simplify and optimize complex processes. Solid business acumen and foundational financial knowledge. Proficiency in English and excellent communication skills. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Empowering our people to shine: Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law. Locations Zurich, SwitzerlandLexington, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time

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