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Senior Research Associate/Research Investigator

Takeda Pharmaceutical - Lexington, MA

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Job Description

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 Senior Research Associate/Research Investigator 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:Perform LC and CE-based assays to support in-house studies such as compatibility, product stability and product characterization.Be a subject matter expert in biochemical assays such as LC-based methods (RP, SEC, CEX) and CE-based methods (CE-SDS, icIEF) to assess purity, oligosaccharide and surfactant of biologics-based productsPrepare fit-for-purpose method qualifications, contributing to CMC sections of regulatory documentsProvide mentorship to team members with a focus on scientific/technical skills associated with assays (LC-based) utilized for release and stability of protein-based biotherapeutics.Understand project timelines and deliverables and plans/coordinates project work within AD US and with other functions in Pharmaceutical SciencesDevelop, implement and perform biochemical analyses via LC and CE-based methods in the lab for biotherapeutics and emerging modalities.Perform fit-for-purpose method qualifications for different biochemical assays.Provide feedback on interpretation and outcome of study results from a technical perspective.Review, interpret and communicate data internally and cross-functionally (e.g., to supervisor, project teams) and prepares technical reports.Plan and implement resolutions to technical problemsIndependently design and execute experiments, and reports resultsInfluence and support initiatives to guide scientific and technical improvement within function and cross-functionally.Author and review technical documents such as protocols, and reports with guidanceHelps develop project strategy and communicates complex data/decisions within department and cross functionallyMinimum Requirements/Qualifications:Associates degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science and 4+ years relevant industry experience (Associate + 7 years for Research Investigator)Bachelors degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 2+ years relevant industry experience (Bachelors + 5 years for RI)Masters degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 0+ years relevant industry experience (Masters + 3 years for RI)Experience working in a matrixed and cross-functional team environmentsHands-on experience with a broad variety of biochemical testing applications including Liquid Chromatography (RP, SEC, CEX) and Capillary Electrophoresis (CE-SDS, icIEF) to assess purity, oligosaccharide and surfactant properties of biologics productsExperience with chromatographic and CE software such as Empower, Chromeleon, 32Karat.Hands-on Experience with as many of the following instruments is a plus: LabChip, PA800, iCE3, HPLC/UPLC.Conduct troubleshooting for complex technical issues for biochemical assaysFamiliarity with method qualification, qualification of assay controls desirableKnowledge with GMP and regulatory guidelines and prior experience on a project team desirableWhat 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

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