
Scientist
Lexington, Massachusetts- Job Level: Senior
- Travel: Minimal (if any)
Takeda has been translating science into breakthrough medicines for 240 years. Every step of the way, our teams have worked together to tackle some of the most challenging problems in drug discovery and development. Today, we’re a driving force behind innovative therapies that make a lasting difference to millions of patients around the world.
In R&D, all of our history and potential comes together in an environment that welcomes diversity of thought and amplifies every voice. Working closely with colleagues, you’ll play a key role in bringing our rich pipeline of products forward to help patients. Come join a team that’s earned trust for more than two centuries, and find out how advancing transformative therapies at Takeda will shape your bright future.
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Job Description
Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:
JOB LOCATION: Lexington, MA
POSITION: Scientist
POSITION DESCRIPTION: Takeda Development Center Americas, Inc. is seeking a Scientist with the following duties: Provide theoretical/conceptual input to the design, development and execution of research assignments (e.g., formulation screening by design of experiment, analyze data and create predictive models for protein stability); plan and execute characterization and optimization experiments (protein conformation and chemical stability) and develop new screening tools (e.g., chromatography, protein particle analysis); review, interpret and communicate data cross-functionally teams; understand drug product developmental project timelines and deliverables; plan, coordinate and communicate project strategy and complex data/decisions (e.g., protein stability data, drug product manufacturing process data) with departmental, functional and external stakeholders to support clinical studies and commercial. Up to 20% remote work allowed.
REQUIREMENTS: Ph.D. degree in Biochemistry and Molecular Biology or related field plus 1 year of related experience. Prior experience must include: Characterize, analyze and evaluate biologic drug substances or drug products with biochemical and biophysical techniques including liquid chromatography (LC), electrophoresis, peptide mapping, glycan mapping, quantitation of polysorbates, silver staining, freeze-drying microscopy (FDM), differential scanning calorimetry (DSC), differential scanning fluorimetry (DSF), subvisible particle analysis via micro-flow imaging (MFI) and HIAC system, FTIR, osmolality measurement, etc.; Develop and qualify analytical test method such as the quantitation of the polysorbates in drug products and drug substances, design studies according to the ICH guidelines to quantitatively evaluate the linearity, intermediate and repeatability precision, specificity, limit of detection, limit of quantitation of the method, and set the acceptance criteria of test results; Setup and manage stability studies using aseptic techniques to aliquot samples, assigning sampling timepoints according to long-term, intermediate or accelerated storage conditions, collecting samples accordingly and allocating testing among colleagues and CRO partners, analyzing result and communicating cross-functionally; Design studies to isolate and characterize the subject biologic materials such as polysaccharides, proteins and nucleic acids; Perform experiments such as cell or tissue culture, preparation and screening of hybridomas for monoclonal antibody, polymerase chain reaction (PCR), liquid chromatography (LC), gas chromatography (GC), electrophoresis, mass spectrometry (MS), nuclear magnetic resonance (NMR), immunoassays, lyophilization, dynamic light scattering (DLS), UV-Vis spectroscopy, etc.; Troubleshoot throughout the process to improve analytical methods and enhance yield; Analyze the data, draw conclusions from the results, and propose scientific and industrial applications of the study.
Full time. $111,800 - $191,600 per year. Competitive compensation and benefits.
Qualified applicants can apply at https://jobs.takeda.com. Please reference job #R0161093. EOE
Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.
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