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’sPrivacy 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 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: Cambridge, MA POSITION: Associate Scientist, CMC Analytical POSITION DESCRIPTION: Takeda Development Center Americas, Inc is seeking a Associate Scientist, CMC Analytical with the following duties: Contribute independently to development of appropriate scientific methods, implementation of evolving scientific technology and working cross functionally with peers to execute program strategy; Independently design and execute experimental plans within function; Independently propose and implement resolutions to technical challenges; Responsible for significant technical leadership within program(s); Serve as a technical resource within function, mentoring and training junior employees; Review and interpret data, communicating clearly to functional leadership and relevant line functions; Support technology transfer internally and externally (documentation, troubleshooting); Assist with development of project strategy within Analytical Development and cross-functionally; Contribute to document preparation for regulatory filings to global health authorities; work on multiple programs; Complete all required training appropriate to role and function in a timely manner; up to 20% remote work allowed. REQUIREMENTS: Bachelor’s degree in Chemistry, Biochemistry, Pharmacy or related field plus 4 years of prior experience. Prior experience must include: Develop analytical methods for pharmaceutical raw materials, in-process controls, drug substance, and drug product utilizing analytical methodologies including HPLC, GC, Karl-Fisher titrator, Dissolution, FT-IR, UV-Vis, and wet chemistry techniques; Optimize and execute separation assays to characterize and quantify small molecules, oligonucleotides and mRNA using LC (Reverse phase and anion exchange chromatography); Author and execute analytical method validation/qualification plans, and method transfer protocols; Support technology transfer internally and externally with contract manufacturing organizations (CMOs), contract testing organizations (CTOs); Work and coordinate with internal and cross-functional peers to execute program assignments with limited supervision. Full time. $96,600.00 - $165,600.00 per year. Competitive compensation and benefits. Qualified applicants can apply at Please reference job #R0142573. 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. Locations Boston, MAWorker Type EmployeeWorker Sub-Type RegularTime Type Full time--s-p-m1-- By applying, you consent to your information being transmitted by Monster to the Employer, as data controller, through the Employer’s data processor SonicJobs. See Takeda Pharmaceutical Terms of Use at and Privacy Policy at and SonicJobs Privacy Policy at and Terms of Use at
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