
Associate Director-Process Engineer SM API Process Sci
Boston, MassachusettsOn the Global Manufacturing and Supply (GMS) team at Takeda, you’ll be part of a rapidly transforming industry that’s applying technology and data in new ways. Within our agile, innovative, people-centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms:
- Small Molecules
- Biologics
- Plasma
- Cell and Gene
As part of the GMS team, you'll have the opportunity to pursue unique experiences and build new skills, and you'll know that the work you do every day makes an impact — on our patients, our people, our planet, and on yourself.
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’sPrivacy Noticeand 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
Title: Associate Director-Process Engineer SM API Process Sci
Location: Cambridge, MA (Hybrid)
About the role:
As an Associate Director-Process Engineer SM API Process Sci, you will provide process engineering support in batch or continuous API platforms through application of chemical engineering and process chemistry fundamentals from clinical to commercial stage. You will also Integrate mechanistic modelling, process simulation, and analysis into current and future processes (as part of product Life-Cycle Management) to enhance process understanding and controls. You will Identify and implement continuous improvement opportunities related to equipment and processes as a core member of a cross-functional process team and provide support to marketing applications for Global markets as well as play a key role in responding to RtQs from Global Health Authorities.
How will you contribute:
Leads the GMSci, Global Process Science, Small Molecules API Manufacturing Science organization ; may serves as Takeda’s expert on small molecule API process and technologies.
Provides strong leadership for the following activities, along with Pharmaceutical Sciences and/or Operation Units: API Manufacturing Process Characterization, Technology Transfer from/to external CMOs and/or internal manufacturing sites. Process validation, Risk assessment, Global expansion, COGs management, Regulatory Activities, Process / Product knowledge.
Leads projects within Takeda product portfolio, both development and commercial, to support Small Molecules API Manufacturing Sciences activities.
Develops and implements strategies for the continuous improvement on the manufacturing of Marketed Products in the late phase of the product life cycle.
Leads the team to implement the manufacturing strategy for key Takeda products at internal manufacturing network and external CMOs.
Leads the effort to create systems and procedures for best practice in commercial technology transfer, process validation.
Leads the team that serves as the central hub of manufacturing process knowledge and establishes system and procedures to ensure the expertise and process knowledge are shared across global Takeda products and sites.
Accountable for successful collaboration with
Other functions within GMS such as API in Onco&ES SM OpU, Network strategy in Strategy & Business Excellence etc.
o Manufacturing Operating Unit Site leads.
o Local Technical Services functions.
o Pharmaceutical Sciences counterparts.
o Other key functional groups such as Global Quality, Regulatory CMC etc.
Leadership
Provide vision and strategy for manufacturing technology projects
Ability to lead and influence the local MSci organization for global manufacturing strategy alignment.
Effectively communicate Global Manufacturing Sciences visions across the functions.
Understanding of API manufacturing from phase appropriate development stage to commercial scale.
Must have sound understanding of Organic Chemistry/Pharmaceutical chemistry.
Ability to work within a multi-functional team (i.e., Engineering, Manufacturing Operations, Manufacturing Sciences, CMC team etc.).
Utilize root cause analysis techniques to investigate process and equipment issues and deliver robust and sustainable corrective and preventative actions in a cross-functional team.
Provide SME support for Due Diligence of M&A and other in-licensing activities.
Lead/support the tech transfer of new processes and unit operations across batch and continuous processing platforms.
What you bring to Takeda:
MS/PhD in Chemical or Process Engineering or Pharmaceutical Engineering.
At least 5+ years’ experience in a cGMP environment.
At least 5+ years of pharmaceutical industry experience in small molecules is preferred.
Must be self-motivated, have good interpersonal skills, capable of analyzing and solving complex problems through innovative thought and experience.
Strategic enterprise thinking, finding innovative ways to serve patients build reputation and trust.
Creating the environment that inspires and enables people.
Focusing on the few priorities and provide superior results.
Elevating capabilities for now and the future.
#GMSGQ
#ZR1
#LI-MA1
#Hybrid
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, MAU.S. Base Salary Range:
$153,600.00 - $241,340.00The 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-termincentives. 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, MAWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeJob Exempt
YesIt 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.Working at Takeda
-
Inclusion
Here, you will feel welcomed, respected, and valued as a vital contributor to our global team. -
Collaboration
A strong, borderless team, we strive together towards our priorities and inspiring mission. -
Innovation
Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients. -
Top Workplace
Recognized for our culture and way of working, we’re one of only 17 companies to receive Top Global Employer® status for 2025. -
Work-Life
Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family. -
Empowerment
Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
We're Steadfast In Our Commitment to Four Key Imperatives
Patient
Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
People
Create an exceptional people experience.
Planet
Protect our planet.
Data & Digital
Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.
Jobs for you
- Qualified Person (QP) Pécs, Hungary Category: Plasma Management
- Medical Therapy Area Lead – GI/HAE, East Gulf & Levant United Arab Emirates Category: Medical Affairs
- Regulatory Affairs Specialist Seoul, South Korea Category: Regulatory Affairs
- Principal Software Engineer Bengaluru, India Category: Data, Digital and Technology
