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 Join us as an End-to-End Supply Chain Planner supporting the vaccine portfolio. This role has the same end-to-end supply-chain scope as the biologics planning role but requires specific experience in vaccine supply chains and launch environments. You will support supply planning during a critical launch and portfolio-development phase, working across manufacturing sites, regional teams, commercial stakeholders, quality, regulatory affairs, medical, and other functions. The successful candidate will combine strong supply-chain expertise with a strategic mindset. You will need to assess changing information—including test results, quality findings, demand assumptions, regulatory developments, and launch requirements—and determine how the supply plan should be adapted. This role requires someone who can connect strategic portfolio priorities with practical execution, anticipate the implications of lifecycle-management activities, and build alignment across a broad and senior stakeholder network. How You Will Contribute Reporting to the End-to-End Supply Chain Lead, you will: Develop and own end-to-end supply plans for the Qdenga vaccine portfolio across short-, medium-, and long-term planning horizons. Support supply planning through the launch phase, including launch readiness, launch execution, market expansion, and post-launch stabilization. Translate vaccine demand, market priorities, manufacturing constraints, testing outcomes, quality information, and regulatory requirements into actionable supply plans. Continuously assess whether the supply plan remains appropriate as new test results, evidence, market information, or launch assumptions become available. Reshape supply, capacity, inventory, allocation, deployment, and production plans when new information requires a change in direction. Coordinate supply planning across manufacturing sites and regional or local market teams. Lead cross-functional supply reviews involving manufacturing, quality, regulatory affairs, medical, commercial, finance, procurement, logistics, and other relevant stakeholders. Develop scenarios and recommendations that balance patient access, supply continuity, quality, compliance, launch timing, inventory, capacity, and cost. Manage the supply-chain implications of vaccine lifecycle-management activities, including launches, market expansion, manufacturing or process changes, product changes, capacity changes, network changes, and future portfolio requirements. Assess how lifecycle decisions affect testing, release, manufacturing capacity, production timing, shelf life, inventory, distribution, market allocation, and service performance. Establish clear launch-readiness plans with milestones, dependencies, owners, risks, decision points, and escalation routes. Build and maintain strong stakeholder networks across global, regional, local, and external organizations. Influence stakeholders and create alignment where market priorities, manufacturing constraints, quality requirements, and launch timelines may differ. Translate strategic vaccine-portfolio priorities into executable supply-chain plans. Provide senior stakeholders with clear scenarios, risk assessments, recommendations, and decision support. Incorporate lessons learned, test results, and launch experience into revised planning assumptions and future lifecycle strategies. Drive continuous improvement in launch governance, supply planning, stakeholder alignment, and cross-functional ways of working. Communicate complex vaccine supply-chain issues clearly to senior stakeholders and leadership teams. Qualifications Bachelor’s degree in supply chain, logistics, business administration, industrial engineering, pharmaceutical sciences, life sciences, or a related field. Minimum of seven years of relevant experience in supply chain planning, production planning, supply network management, or a related pharmaceutical operations discipline. Demonstrated experience in the vaccine industry or vaccine supply chain. Experience supporting a vaccine launch, product introduction, launch-readiness program, market expansion, or a comparable complex pharmaceutical launch. Strong understanding of vaccine manufacturing, testing, quality, release, regulatory requirements, allocation, distribution, and market supply. Experience managing supply planning across multiple manufacturing sites, products, markets, or production stages. Experience in vaccine or pharmaceutical product lifecycle management, including launches, transfers, process or product changes, market expansion, capacity changes, network changes, and discontinuations. Demonstrated ability to interpret test results, quality data, regulatory information, demand changes, and market inputs and translate them into revised supply plans. Strong strategic mindset, with the ability to connect portfolio strategy and launch priorities to practical supply-chain execution. Strong stakeholder-management and influencing skills across global, regional, local, and external organizations. Ability to work effectively in a complex and evolving launch environment. Proven ability to develop scenarios, assess risks, make recommendations, and drive decisions through governance forums. Strong analytical, communication, negotiation, and presentation skills. Experience with SAP and/or advanced planning systems such as IBP or OBP. Strong Excel skills and experience with reporting tools such as Qlik or Power BI. Ability to influence without direct authority in a matrix organization. Fluency in English; additional language skills are an advantage. Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: Lexington, MA U.S. Base Salary Range: $137,000.00 - $215,270.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. For information about our benefits, please click here. EEO Statement 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, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations Lexington, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own. Takeda is an equal opportunity employer. For applicants of U.S and Puerto Rico positions: Click here to learn about our commitment to Equal Employment Opportunity (EEO). If you are limited in the ability to use our job application tool, or otherwise require a reasonable accommodation for a disability please click here.

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