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Senior​/Principal Scientist, Analytical Cell Line Engineering and Bioassay Development

Job in Lexington, Middlesex County, Massachusetts, 02173, USA
Listing for: Takeda
Full Time position
Listed on 2026-07-19
Job specializations:
  • Research/Development
    Biotech Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 154400 - 242550 USD Yearly USD 154400.00 242550.00 YEAR
Job Description & How to Apply Below

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Job Description

Join Takeda as a Senior/Principal Scientist, Analytical Cell Line Engineering and Bioessay Development who plays a key role in managing and performing scientific research, development, and testing of new products, manufacturing processes, and raw materials. This role contributes to Takeda’s mission by developing and implementing new products, processes, and standards that impact functional results. As a senior technical expert within the function, you will apply deep scientific expertise in analytical cell line engineering and bioassay development to anticipate technical challenges, recommend improvements, and provide consultative guidance across programs.

You will operate independently, lead complex technical work streams, mentor colleagues, and contribute to technical standards, regulatory‑ready documentation, and capability development within Analytical Development and Quality Control Biologics.

About the role

You will report to the Associate Director, Analytical Cell Line Engineering and Bioassay Development, within the Analytical Development and Quality Control (Biologics) team. You will design, generate, characterize, and manage analytical cell lines that serve as critical reagents for potency assay development, functional characterization, and analytical control strategy. Operating at the interface between Discovery, Global Biologics, Analytical Development, and late‑stage potency teams, this role translates product mechanism of action into scientifically sound, phase‑appropriate cell line and assay strategies.

You will lead complex technical work streams, solve scientific problems, contribute to regulatory documentation, and help establish scalable approaches for analytical cell line engineering and bioassay development. At the Principal Scientist level, you will serve as a subject‑matter expert, influence cross‑program strategy, and contribute to technical standards and capability development. This is an individual‑contributor technical leadership role with responsibility for mentoring junior scientists and leading technical work across programs.

How

you will contribute
  • Lead the design, generation, characterization, and lifecycle management of stable mammalian analytical cell lines expressing targets of interest, receptor systems, or reporter constructs to support potency and functional bioassays.
  • Develop and implement technical approaches for plasmid and vector design, transfection or transduction, stable integration, clone screening, clonal isolation, genomic and copy number characterization, expression stability, and analytical cell banking.
  • Translate product mechanism of action into cell line designs and cell‑based assay concepts aligned with potency and analytical control strategy.
  • Develop and support cell‑based bioassays, including reporter gene assays, signaling pathway assays, proliferation or cytotoxicity assays, and other mechanism‑based functional readouts.
  • Contribute to early‑stage potency assay development and ensure effective technical continuity with late‑stage potency, validation, transfer, and QC implementation strategies.
  • Evaluate assay and cell line performance attributes, including sensitivity, specificity, robustness, stability, reproducibility, and fitness for intended use.
  • Independently design and execute complex experimental plans, interpret data, identify technical risks, and recommend scientifically justified solutions.
  • Represent Analytical Development on cross‑functional program teams and provide technical input on potency strategy, functional characterization, cell line suitability, and control strategy.
  • Author and review technical reports, protocols, method documents, cell line characterization packages, technology transfer documents, and CMC source documentation supporting regulatory submissions.
  • Ensure that…
Position Requirements
10+ Years work experience
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