Takeda
Direct Workday career site

Drug Product Development Associate Scientific Fellow

Location
Lexington, MA
Listed
3 days ago

About the role

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.

About the role

The Drug Product Development Associate Scientific Fellow is involved in the development of Takeda's parenteral products, including monoclonal antibodies, recombinant proteins, peptides, antibody-drug conjugates, and small molecules. You will participate in cross-functional Chemistry, Manufacturing, and Controls(CMC) teams and lead all drug product activities for one or more programs.

Responsibilities include developing robust liquid or lyophilized formulations for drug substance and drug product throughout the product life cycle, as well as developing and transferring scalable and robust drug product manufacturing processes from early phase through process validation.

This role supports Takeda's mission by developing and implementing drug product presentations and manufacturing processes to deliver new medicines to patients.

How you will contribute

  • As a member of the CMC team for one or more programs, lead all parenteral drug product development activities with a high level of independence
  • Collaborate with key partners such including Analytical Development, Drug Substance Development, Device Development, Quality, Commercial Manufacturing, and Clinical development to ensure delivery of the cross functional project needs
  • Design and execute phase-appropriate DP formulation development, process development, and process characterization studies
  • Provide technical leadership for clinical drug product process development and clinical drug product manufacturing
  • Lead the design and execution of PPQ for validation of late-stage processes
  • Author and review development documents including regulatory submissions and responses
  • Identify, evaluate, adopt, and develop formulation and drug product technologies to continuously improve product development capabilities
  • Support drug product manufacturing deviation investigations, CAPAs, and change control management
  • Communicate with leadership and provide guidance in the most complex situations
  • Mentor team members and share subject matter knowledge across the function

Skills and qualifications

  • PhD in chemistry, biochemistry, pharmaceutical sciences, or a related field, and 7 or more years of relevant experience, or a Master's degree in chemistry, biochemistry, pharmaceutical sciences, or a related field, and 13 or more years of relevant experience, or a Bachelor's degree in chemistry, biochemistry, pharmaceutical sciences, or a related field, and 15 or more years of relevant experience
  • Recognized expert in drug product development, with deep knowledge of liquid and lyophilized formulation development and aseptic fill/finish process development
  • Analytical and problem-solving skills are required. Able to troubleshoot critical issues or problems using appropriate information and determine causes and possible solutions
  • Experienced and demonstrated track record in biopharmaceutical product development including but not limited to drug product development, drug product process characterization, QbD, and control strategy
  • Expert in innovation, recognized internally or externally as a thought leader, capable of coaching others and driving strategic ideation for novel or improved products and technologies
  • Possesses expert-level writing skills, recognized for strong command of language, structure, and content creation, capable of coaching others and setting writing standards
  • Experienced in lyophilization and/or combination drug product development with good understanding of the inter-relationship among formulation parameters, process parameters, product delivery, and quality
  • Excellent communication, technical, organizational, interpersonal and leadership skills are required
  • Must be a team player prepared to lead, work effectively and efficiently in a team-based environment

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

$154,400.00 - $242,550.00

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.

Read the original posting

From Takeda's careers page, first listed on Rolev.ai on November 6, 2026. Rolev.ai is not the employer.

How Rolev.ai helps with this application

Rolev.ai is a job search and application tool for US job seekers. For this Drug Product Development Associate Scientific Fellow role at Takeda, it shows how your resume fits, tailors your resume to the posting, and prepares the application for you to review.

  • See how you fit

    Openings from employer career sites are ranked against your whole resume—and searchable inside Claude, ChatGPT, and Cursor via Rolev.ai MCP.

  • Tailor without inventing

    Every change to your resume is checked against your original. New experience goes in only with your yes—zero fabricated claims.

  • Draft the full kit

    Tailored and Full Match resumes, role-specific cover letters, and answers to employer screening questions are prepared in seconds.

  • 1-Click Extension Autofill

    The Chrome extension fills the employer's Greenhouse, Workday, Lever, or Ashby form in 1 click. You review it and press Submit.

Common questions

Where is the Drug Product Development Associate Scientific Fellow job at Takeda located?

This Drug Product Development Associate Scientific Fellow position at Takeda is located in Lexington, MA. Always check Takeda's application page for specific state eligibility or relocation policies.

How do I apply for the Drug Product Development Associate Scientific Fellow position at Takeda?

This listing links directly to Takeda's Workday application page. You can apply directly on Takeda's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.