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Date Posted
Today
New!Remote Work Level
Hybrid Remote
Location
Hybrid Remote in Lexington, MA
Job Schedule
Full-Time
Salary
$100,755 - $141,240 ANNUALLY
Benefits
401k Matching/Retirement Savings Dental Insurance Health/Medical Insurance Vision Insurance Paid Holidays Paid Sick Leave Paid Vacation
Categories
Job Type
Employee
Career Level
Entry-Level
Travel Required
Yes
Education Level
Bachelor's/Undergraduate Degree
About the Role
Title: Digital Drug Product Development Senior Research Associate
Location: Lexington United States
Job ID R0191461Category Pharmaceutical SciencesSubcategory Research & DevelopmentBusiness Unit Research & DevelopmentJob Type Full time
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(opens in new window) and Terms of Use(opens in new window). I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:
JOB LOCATION: Lexington, MA
POSITION: Digital Drug Product Development Senior Research Associate
POSITION DESCRIPTION: Takeda Development Center Americas, Inc. is seeking a Digital Drug Product Development Senior Research Associate with the following duties: develop robust drug product formulations across the product lifecycle, including development and tech transfer of scalable, robust drug product manufacturing processes from early phase through process validation; apply computational fluid dynamics (CFD) with a strong focus on mixing and filtration operations to understand, design, and optimize drug product unit operations; utilize CFD principles and tools (including M-Star CFD) to build and deploy digital twins of drug product development processes, enabling mechanistic understanding of mixing, suspension uniformity, shear exposure, filtration performance, and scale-up risk; provide technical leadership and guidance for formulation and drug product development, author technical protocols, design and execute experiments, generate technical reports, and contribute to CMC sections supporting regulatory submissions; lead and support in silico, simulation, and digital twin initiatives, integrating CFD-based mixing and filtration models with experimental data; apply modern computational approaches including machine learning, data analytics, statistical and chemometric methods—to traditional pharmaceutical formulation and process development challenges; deliver applied data science, predictive modeling, and mechanistic process modeling support across multiple projects to enable robust process development, scale-up, and validation. Up to 10% domestic travel required for conference presentations, and site visits of CDMO and manufacturers. Up to 20% remote work allowed.
Estimated salary range reflects expected pay for this role. Actual base salary depends on the applicant’s qualifications, experience, skills, education, certifications, & work location, & will comply with all applicable minimum‑wage laws. U.S. employees may be eligible for medical, dental, & vision insurance, 401(k), paid time off, sick leave, company holidays, incentive compensation programs, & other benefits offered under company policies.
REQUIREMENTS: Master’s degree in Biotechnology or related field OR Bachelor’s degree in Biotechnology and 2 years of related experience. Prior experience must include: construct 3D geometric models using AutoCAD and SolidWorks and apply Computational Fluid Dynamics (CFD) using M Star CFD to simulate mixing studies, filtration studies, hydrodynamics, heat and mass transfer, transport phenomena, evaluate mixing time, mixing speed, power number, and scale effects in drug product manufacturing systems; develop mechanistic computational process models for mass, momentum, and energy balances and implement simulations, parameter estimation, and scenario analysis using Python and R to support biopharmaceutical process and product development understanding and risk assessment; design, execute, and support drug substance and drug product manufacturing processes, including technology transfer, equipment operation and troubleshooting, process validation studies, scale up and scale down model development, assay and media preparation, microbial biologics and monoclonal antibody production using perfusion and fed batch bioreactors; conduct site acceptance testing for equipment for lab equipment. Programming recipes into Delta V as a Delta V superuser & measure tanks, bags and process developed using multiple scales (Scale up and scale down) in pilot & manufacturing scale.
Full time. $100,755 to $141,240 per year.
Qualified applicants can apply at https://jobs.takeda.com(opens in new window). Please reference job #R0191461. EOE
Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.
Locations
Lexington, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time