Lead Process Scientist, Drug Product (Sr. Manager)

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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 transfer to internal sites and external contract manufacturing organizations (CMOs)

  • Process validation planning and execution support

  • Process characterization and establishment of process understanding

• Serve as an escalation point for complex technical investigations and issue resolution, mobilizing and coordinating rapid cross-site support when needed.

• Drive manufacturing strategies for 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.

• Lead continuous improvement for 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 is captured, shared, and reused across 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) in Chemistry, Chemical Engineering, or a related discipline (or equivalent combination of education and experience).

• At least 5 years of relevant industry experience, with experience supporting pharmaceutical development and/or manufacturing in DP-related areas (e.g., OSD and/or parenterals).

• Demonstrated success as an SME and project leader in a matrix environment, influencing technical decisions across functions and sites without relying on direct authority.

• Strong working knowledge of DP manufacturing technologies, validation and tech transfer principles, and practical application of industry best practices.

• Experience contributing to or leading regulatory CMC readiness, including converting process understanding into clear technical narratives and defensible control strategies.

• Proven ability to analyze 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 prioritizes focus, 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, 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.