Analytical Method Development Scientist - In-Process

Takeda Pharmaceutical Co.; Cambridge (MA); On-site; USD 104,000 - 163,000; Full time

Job summary

Takeda Pharmaceutical Co. in Cambridge, MA, seeks an experienced analyst to independently design, develop, qualify, and report fit-for-purpose analytical methods for in-process testing of synthetic molecules.

You will partner with in-process teams to ensure seamless method transfer and lifecycle management, applying AQbD principles and validating automation and PAT platforms. The role requires 3–7+ years of lab experience with techniques such as HPLC/UPLC, GC/GC-MS, FT-IR, NMR, Karl Fischer, 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.
• Hands-on laboratory experience is required.
• Experience with analytical techniques for in-process testing of synthetic molecules.
• Ability to plan, execute, analyze, and report method development experiments.
• Ability to prepare and review technical documentation and transfer materials.

Responsibilities

• Independently design, develop, qualify and report fit-for-purpose analytical methods for in-process testing.
• Collaborate with cross-functional teams to transfer methods and manage lifecycle.
• Apply AQbD principles and support technology transfer activities.
• Validate and integrate automation, digital tools, and PAT platforms.

Skills

Analytical method development

AQbD principles

Data interpretation

Documentation

Communication

Team collaboration

Problem solving

Education

Bachelor's degree in a relevant field

Master's degree in a relevant field

Associate degree

Tools

HPLC/UPLC

GC/GC-MS

FT-IR

NMR

Karl Fischer

ELN/LIMS

Laboratory automation

Job description

Takeda Pharmaceutical Co. in Cambridge, MA, seeks an experienced analyst to independently design, develop, qualify, and report fit-for-purpose analytical methods for in-process testing of synthetic molecules.

You will partner with in-process teams to ensure seamless method transfer and lifecycle management, applying AQbD principles and validating automation and PAT platforms. The role requires 3–7+ years of lab experience with techniques such as HPLC/UPLC, GC/GC-MS, FT-IR, NMR, Karl Fischer, and