Takeda

Senior Scientist, Biologics Process Analytical Method Development

Takeda$137K — $215K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D., MSc., or BSc. in analytical chemistry, biochemistry, or related field with relevant industry experience (3-11 years).
  • Demonstrated leadership in managing process analytical development programs.
  • Strong background in chromatographic and electrophoretic assay development.
  • Experience in validation and life cycle management of analytical methods using AQbD principles.
  • Familiarity with ICH guidelines and regulatory requirements for method development.
  • Excellent communication skills, both verbal and written.
  • Experience with laboratory automation technologies is highly desirable.

Responsibilities

  • Lead analytical method development for biologics processes and serve as the main contact for testing teams.
  • Develop, optimize, and implement high-throughput analytical methods using AQbD principles.
  • Collaborate with Analytical Development and Quality teams for method bridging and transfer.
  • Support lifecycle management of analytical methods, including documentation and troubleshooting.
  • Integrate laboratory automation into analytical processes in collaboration with subject matter experts.
  • Serve as a resource and trainer on analytical technologies for team members and interns.
  • Evaluate new analytical tools and laboratory automation solutions as needed.

Benefits

  • Medical, dental, and vision insurance options.
  • 401(k) plan with company match benefits.
  • Tuition reimbursement program for ongoing education.
  • Generous paid time off including vacation and sick days.
  • Paid volunteer time off to support community engagement.
  • Short-term and long-term disability coverage.
  • Well-being benefits to support overall employee health.
Full Job Description
Job Description

About the role:
The Senior Scientist, Biologics Process Analytical Method Development is responsible for leading in-process analytical method development for biologics programs. In this role, you will partner with Biologics Process Development, Analytical Development, Quality, and Stability teams to develop, transfer, and sustain high-throughput analytical methods that support process and product development. You will apply phase-appropriate approaches and Analytical Quality by Design principles, integrate automation where appropriate, and provide clear scientific input that supports process development decisions.

How you will contribute:
  • Lead in-process analytical method development needs and serve as the main contact for biologics process development, and in-process testing teams.
  • Develop, optimize, transfer, and sustain high-throughput, fit-for-purpose analytical methods for biologics development using phase-appropriate approaches and Analytical Quality by Design (AQbD) principles.
  • Partner with Analytical Development, Quality, Compliance, and Stability teams to support method bridging, transfer, and an analytical results continuum for biologics programs.
  • Support the transfer, training, implementation, and lifecycle management of methods in process development laboratories, including documentation and troubleshooting plans.
  • Work with automation subject matter experts to validate and integrate laboratory automation platforms into process analytical methods.
  • Serve as a scientific resource and trainer for analytical and automation technologies, including support for new team members and interns.
  • Evaluate new tools, platforms, and vendor solutions for laboratory automation and analytics as needed.


What you bring to Takeda:
  • Ph.D. MSc. or BSc. in analytical chemistry, chemistry, biochemistry, or related field with minimum of 3 years (Ph.D.) 6 years (MS) or 11 years (BS) of relevant industry experience.
  • Proven experience leading and managing programs, preferably in process analytical development functions.
  • Strong expertise in developing chromatographic (U/HPLC), electrophoretic and isoelectric focusing (CE-SDS/Maurice®/Lab Chip GXII®) and/or ELISA type assays.
  • Experience in development, phase-appropriate validation, transfer and life cycle management of analytical methods using AQbD principles.
  • Knowledge on ICH and other regulatory guidance on analytical method development and life cycle management.
  • Must have effective communication skills, including verbal, written, and scientific data presentation.
  • Experience with laboratory automation capabilities, such as liquid handlers, dispensers, SCARA robots, and mobile robots, is highly desirable.
  • Experience with laboratory information management systems and other digital or AI tools is desirable.


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:
$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.

Locations
Lexington, 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.

About Takeda

Takeda Pharmaceutical Company Limited is a global pharmaceutical company that develops and markets pharmaceutical products. The company's products are used to treat a wide range of medical conditions, including cardiovascular and metabolic diseases, respiratory diseases, and cancer. Takeda Pharmaceutical Company Limited was founded in 1781 and is headquartered in Tokyo, Japan. The company has operations in more than 80 countries and employs more than 49,000 people worldwide.
Learn more about Takeda
Size
47,347 employees
Market Cap
$48.2 billion
Industry
Founded
1781
5 Year Trend
+15.6%
NASDAQ

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