Senior Manager, Manufacturing Science (MSAT) – Drug Substance (Small Molecules)

Company: Takeda
Location: Lexington
Posted on: March 2, 2026

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 In this role, you will serve as Takeda’s senior subject matter expert for synthetic drug substance manufacturing across the full product lifecycle. In this high?visibility, high?impact role, you will define and execute the technical strategy that underpins robust, reliable, and sustainable global API supply. You will apply deep expertise in small molecule and/or ADC drug substance manufacturing to shape process design, scale?up, technology transfer, and commercial production. As the primary technical point of contact for key programs, you will influence global decision?making, guide complex investigations, and partner closely with cross?functional leaders in Quality, Regulatory, Analytical Sciences, Supply Chain, and R&D. This position is ideal for a seasoned process scientist who thrives on solving complex technical challenges, driving manufacturing excellence, and ensuring supply continuity for patients worldwide. How You Will Contribute Lead phase?appropriate process design, scale?up, technology transfer, and commercial manufacturing support for small molecule and ADC drug substance, setting technical strategies that enable efficient clinical and commercial supply. Serve as the senior technical authority for assigned programs, providing expert guidance, resolving complex manufacturing issues, and driving timely, evidence?based decision?making. Apply statistical and data?driven tools to interpret manufacturing performance, identify root causes, and enable ongoing optimization, improved process robustness, and continuous improvement initiatives. Manage external manufacturing activities at CROs and CMOs, ensuring strong technical alignment, successful technology transfers, and effective collaboration on troubleshooting and optimization. Author or review key CMC and quality documentation, including validation reports, technology transfer packages, technical reports, and regulatory submission content for IND/IMPD/NDA/MAA filings. Support global regulatory interactions by preparing responses to health authority questions and ensuring documentation meets internal standards and external regulatory expectations. Maintain strong adherence to quality systems—including deviations, investigations, CAPAs, and change controls—while fostering inspection readiness and participating in audits and compliance activities. Apply lifecycle and QbD principles to guide development and commercial programs, contributing to improved process understanding and long?term manufacturing reliability. Identify and support opportunities to enhance sustainability in drug substance manufacturing in line with Takeda’s Planet goals. Translate complex scientific concepts into clear, actionable insights for both technical and non?technical audiences, preparing concise updates and presentations for leadership as needed. Mentor and coach colleagues, helping to elevate technical problem?solving skills and support capability building across the organization. What You Bring to Takeda Advanced degree (MSc or PhD) in Chemistry, Chemical Engineering, Pharmacy, or related discipline. 5 years of pharmaceutical industry experience in small molecule drug substance development, scale?up, and pilot?plant or commercial manufacturing. Strong understanding of regulatory expectations, CMC requirements, and global quality systems. Demonstrated experience writing CMC sections for regulatory filings. Technical proficiency in statistical analysis and data?driven decision?making. Experience with ADC process development/manufacturing is a strong plus. Willingness to travel domestically and internationally. 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. GMSGQ ZR1 LI-MA 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. U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. 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, MAIRL - Dublin - Baggot Street, Zurich, Switzerland 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.

Keywords: Takeda, Boston , Senior Manager, Manufacturing Science (MSAT) – Drug Substance (Small Molecules), Science, Research & Development , Lexington, Massachusetts