Scientist

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda''s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAt Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.Join Takeda as a Scientist where you will support programs in development in Analytical Development. You will also provide theoretical and technical input to the design, execution, and resourcing of complex studies for studies in a cross-functional team. As part of the Analytical Development Testing Group, you will report to Sr Scientist.How you will contribute:Coordinate with cross-functional teams for execution of studies with multi-department stakeholders with a focus project/study management and communication contributing to CMC activities.Prepare, coordinate, and execute fit-for-purpose method qualifications, contributing to CMC sections of regulatory documents.Lead communications to project representatives on study statusExecute Liquid Chromatography, Capillary Electrophoresis and plate-based assays for studies such as in-use compatibility, product stability and product characterization.Provide mentorship to junior members with a focus on scientific/technical skills associated with assays (LC-based, plate-based ELISA assays) utilized for release and stability of biologics.Understand project timelines and deliverables for planning and execution of project studies.Plan and execute fit-for-purpose method qualifications for various biochemical, impurities and binding methods.Establish communication plans for the planning and coordination of in-house testing studies within AD-US and cross-functional teams.Plan and implement resolutions to technical and logistical problems/issue.Review, interprets, and communicates data internally and cross-functionally (e.g., project teams, supervisor, and cross-functional stakeholders).Help with technical troubleshooting of LC, CE-based and plate-based assays.Build and maintain relationships with key stakeholders within AD-US and other functional fluence project strategy by communicating important issues and positions regarding technical study dependently designs, and executes experiments and produce summary of results.Minimum Requirements/Qualifications:Bachelors degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science and 8+ years relevant industry experienceMasters degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 6+ years relevant industry experiencePhD in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 0+ years relevant industry experienceExperience working in a matrixed and cross-functional team environmentsExperience and a passion for technical projects in multi-stakeholder environmentsHands-on experience with a broad variety of biochemical and ELISA-based techniques, including Liquid Chromatography (RP, SEC, CEX), Capillary Electrophoresis (CE-SDS, icIEF), plate-based impurities methods (HCP, residual Protein A, residual DNA), plate-based binding/activity methods for biologics.Experience with chromatographic and CE software such as Empower, Chromeleon, 32Karat.Conduct troubleshooting for complex technical issues for biochemical and plate-based assays.Familiarity with project management and qualification of assay controls is a plus.Knowledge of GMP and regulatory guidelines and prior experience on a project team will be a plus.What Takeda can offer you:Comprehensive Healthcare: Medical, Dental, and VisionFinancial Planning & Stability: 401(k) with company match and Annual Retirement Contribution PlanHealth & Wellness programs including onsite flu shots and health screeningsGenerous time off for vacation and the option to purchase additional vacation daysCommunity Outreach Programs and company match of charitable contributionsFamily Planning SupportFlexible Work PathsTuition reimbursementMore about us:At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply.LI-SB1EEO StatementTakeda 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.LocationsLexington, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Created: 2025-11-15