Lead Process Scientist, Drug Product (Sr. Manager)
Company: Takeda
Location: Boston
Posted on: January 5, 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
Embedded in our Global Manufacturing Science (GMSci) team, you will
provide process science and manufacturing technology leadership for
drug product manufacturing across Takeda’s global network. You will
act as a technical SME for small molecule oral solid dosage and/or
parenteral processes, supporting both new product introductions and
lifecycle management of marketed products. Working in a matrix
environment, you will align cross-functional stakeholders and
external partners to enable robust, compliant, and scalable
manufacturing. You will also represent the drug product process
science perspective in regulatory CMC interactions, translating
process understanding into clear and defensible filing content.
Overall, you will help strengthen how Takeda applies process
knowledge consistently across sites to improve execution and
decision-making. How you will contribute Lead and/or oversee DP
technical deliverables across the product lifecycle, including:
Technology transferto internal sites and external contract
manufacturing organizations (CMOs) Process validationplanning and
execution support Process characterizationand establishment of
process understanding Serve as an escalation point forcomplex
technical investigations and issue resolution, mobilizing and
coordinating rapid cross-site support when needed.
Drivemanufacturing strategiesfor assigned key products, ensuring
the approach is consistent across Takeda’s internal network and
CMOs and is grounded in process knowledge and science-based risk
management. Leadcontinuous improvementfor late-phase/matured
products by identifying and advancing opportunities that improve
robustness, control strategy, and operational performance without
compromising compliance. Partner effectively in a matrix
environment with key stakeholders, including: Pharmaceutical
Sciences counterparts (R&D) Manufacturing site and operating
unit leaders Local Technical Services organizations Global Quality
and Regulatory CMC teams Ensure process knowledge iscaptured,
shared, and reusedacross sites and functions to strengthen Takeda’s
overall DP manufacturing capability and speed decision-making. What
you bring to Takeda Degree(BS, MS, and/or PhD) inChemistry,
Chemical Engineering, or a related discipline(or equivalent
combination of education and experience). At least 5 yearsof
relevant industry experience, with
experiencesupportingpharmaceutical development and/or
manufacturingin DP-related areas (e.g., OSD and/or parenterals).
Demonstrated success as anSME and project leader in a matrix
environment, influencing technical decisions across functions and
sites without relying on direct authority. Strong working knowledge
ofDP manufacturing technologies, validation and tech transfer
principles, and practical application ofindustry best practices.
Experience contributing to or leadingregulatory CMC readiness,
including converting process understanding into clear technical
narratives and defensible control strategies. Proven ability
toanalyze complex problems, drive to root cause, and implement
sustainable solutions with high technical rigor. Communication and
stakeholder-management skills that enable effective collaboration,
conflict resolution, and alignment across internal teams and
external partners. A working style that prioritizesfocus,
accountability, and measurable outcomes, while actively building
capability for the future. 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: Boston, 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 Boston, MABEL - Lessines, Brooklyn Park, MN, CHE -
Glattpark (Opfikon) - Zurich HQ, CHE - Neuchatel, IRL - Bray -
Production, IRL - Dublin - Baggot Street, IRL - Grange Castle -
Production, JPN - Yamaguchi - Hikari Plant, USA - CA - Thousand
Oaks - Rancho Conejo 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, Nantucket , Lead Process Scientist, Drug Product (Sr. Manager), Science, Research & Development , Boston, Massachusetts