Associate Scientist, Process Analytical Method Development

Posted 3 Days Ago
Be an Early Applicant
Cambridge, MA, USA
Hybrid
104K-163K Annually
Senior level
Healthtech • Software • Analytics • Biotech • Pharmaceutical • Manufacturing
Takeda exists to create better health for people, brighter future for the world.
The Role
Develops, qualifies, and reports fit-for-purpose analytical methods for in-process testing of synthetic molecules. Plans experiments, analyzes data, troubleshoots technical issues, prepares technical documentation, and supports process development, stability, manufacturing readiness, technology transfer, comparability, and regulatory submissions. Collaborates with Analytical Development, Quality, Compliance, Stability, automation, digital, and PAT teams. Applies AQbD principles, data integrity practices, and laboratory automation technologies.
Summary Generated by Built In

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Job Description

About the role:
You will report to the Associate Director, Process Analytics Lead within Analytical Development organization. You will contribute to in-process method development activities for synthetic molecules (Small molecules, Oligonucleotides, Peptides) using liquid chromatography, gas chromatography, spectroscopy, Karl Fischer, and particulate matter testing. You will independently plan, execute, analyze, and report method development experiments to support product understanding, process development, comparability, stability, manufacturing readiness, technology transfer, and regulatory submissions. You will work with departmental and cross-functional partners to generate high-quality data, troubleshoot technical issues, and communicate results that support decision-making for synthetic molecule programs. This role does not include direct people management.


How you will contribute:

  • Independently design, develop, qualify and report fit-for-purpose, scientifically sound and high-throughput analytical methods for in-process testing of synthetic molecules under general direction.
  • Work closely with in-process analytical testing team within synthetic molecule process development organization for seamless method transfer and life cycle management.
  • Apply Analytical Quality by Design (AQbD) principles and phase-appropriate approaches for method development.
    Partner with Analytical Development, Quality, Compliance, and Stability teams to support method bridging, and transfer activities.
    Work with automation, digital and PAT subject matter experts to validate and integrate technologies and platforms into process analytical methods.
    Evaluate new tools, platforms, and vendor solutions for in-process analytics as needed.

Skills and qualifications:

  • Typically associate degree with 7+ years, bachelor’s degree with 5+ years, or master’s degree with 3+ years of relevant industry experience in analytical development for synthetic molecules.
  • Previous hands-on experience working in a laboratory setting is required.
  • Strong expertise and practical knowledge of one or more relevant analytical techniques for testing synthetic molecules during process development such as liquid chromatography (HPLC/UPLC), gas chromatography (GC/GC-MS), spectroscopy (FT-IR, NMR), Karl Fischer, and particulate matter testing, or related techniques.
  • Ability to independently plan and execute experiments, analyze data, interpret results, and communicate conclusions to technical and cross-functional stakeholders.
  • Ability to prepare and review technical documentation, including protocols, reports, data summaries, method documents, SOPs, and technology transfer materials.
  • Demonstrated problem-solving skills, including the ability to troubleshoot technical issues, propose practical solutions, and escalate risks appropriately.
  • Ability to work across departmental and cross-functional teams with an understanding of project timelines, deliverables, and data quality expectations.
  • Understanding of data integrity principles, ELN/LIMS documentation, laboratory safety, and good documentation practices.
  • Ability to manage multiple priorities with general direction while maintaining attention to scientific quality, timelines, and documentation standards.
  • Ability to communicate technical information clearly in writing and in conversation, and to present technical information clearly to scientific and project stakeholders.
  • Working understanding of AQbD principles & ICH guidelines.
    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:

Cambridge, MA

U.S. Base Salary Range:

$103,500.00 - $162,690.00

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. 


For information about our benefits, please click here.


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.

LocationsCambridge, MA

Worker TypeEmployee

Worker Sub-TypeRegular

Time TypeFull 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.

Skills Required

  • Associate degree with 7 or more years of relevant industry experience, bachelor's degree with 5 or more years, or master's degree with 3 or more years in analytical development for synthetic molecules.
  • Hands-on laboratory experience.
  • Expertise in one or more analytical techniques, including HPLC/UPLC, GC/GC-MS, FT-IR, NMR, Karl Fischer, or particulate matter testing.
  • Ability to independently plan and execute experiments, analyze data, interpret results, and communicate conclusions.
  • Ability to prepare and review protocols, reports, data summaries, method documents, SOPs, and technology transfer materials.
  • Demonstrated technical problem-solving and troubleshooting skills.
  • Ability to work cross-functionally and manage project timelines, deliverables, and data quality expectations.
  • Understanding of data integrity, ELN/LIMS documentation, laboratory safety, and good documentation practices.
  • Ability to manage multiple priorities while maintaining scientific quality, timelines, and documentation standards.
  • Clear written, verbal, and presentation communication skills for scientific and project stakeholders.
  • Working understanding of AQbD principles and ICH guidelines.
  • Experience with laboratory automation, including liquid handlers, dispensers, SCARA robots, or mobile robots.
  • Experience with LIMS and other digital or AI tools.

Takeda Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Takeda and has not been reviewed or approved by Takeda.

  • Retirement Support — Employer-funded retirement is described as notably strong, combining a dollar-for-dollar 401(k) match with an additional company contribution that scales with age and service. Access to an employee stock purchase plan further supports long-term wealth building.
  • Parental & Family Support — Paid bonding leave for all parents, substantial adoption/surrogacy reimbursement, and robust caregiver resources (backup care and Maven family-forming support) are emphasized as core strengths. These offerings create a comprehensive safety net for a range of family situations.
  • Healthcare Strength — Multiple medical plan options (nationwide PPO/HSA and regional HMOs), employer HSA funding, and integrated mental-health and well-being programs signal depth in coverage. Preventive care is covered in-network, and plan choices by state expand access.

Takeda Insights

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The Company
HQ: Cambridge, MA
50,000 Employees
Year Founded: 1781

What We Do

For over 240 years, Takeda’s propensity to evolve has driven the next generation of innovation, and as a future-focused organization, we’re continuing to drive forward with endurance in our steadfast pursuit to achieve the best outcomes for our patients in a rapidly changing world.  We have been preparing for this period of value creation by investing in data, digital and technology, and we’re proud of our employees and their commitment to turning groundbreaking ideas into life-changing impacts.   Since our founding in Japan, integrity and putting patients first have been at the heart of our identity, and we will emerge ready for our future as one of the most trusted and science-driven digital biopharmaceutical companies. Join a team where your innovation impacts lives.   Together, we’ll realize improved outcomes by improving data quality, enhancing launch execution and improving the patient journey. You’ll play a critical role in accelerating data collection and increasing accuracy across all parts of the business. Patients across the globe will benefit from access to treatments afforded by greater opportunities and efficiency in our research and development.  

Why Work With Us

We connect to our history and Japanese heritage through everything we do to bring our purpose, values, vision, and imperatives to life. We are committed to bringing better health and a brighter future to patients. Being a part of Takeda means having the opportunity to be a part of something bigger than yourself.

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