• Associate Director, Global Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    …Proactively recognizes and contributes to enhancing business processes. As part of the Global Regulatory Affairs CMC team, you will report to the Senior ... Director Global Regulatory Affairs CMC . **How you...long-term disability coverage, basic life insurance, a tuition reimbursement program , paid volunteer time off, company holidays, and well-being… more
    Takeda Pharmaceuticals (07/08/25)
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  • Senior Director, Global Regulatory

    Takeda Pharmaceuticals (Lexington, MA)
    …as follows: + Champions, independently develops and leads the execution of regulatory CMC investigational and/or registration strategies for assigned products as ... guide the team to define and drive strategy for CMC regulatory dossier content and reviews this...long-term disability coverage, basic life insurance, a tuition reimbursement program , paid volunteer time off, company holidays, and well-being… more
    Takeda Pharmaceuticals (04/30/25)
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  • Director, Pharmaceutical Sciences Program

    Takeda Pharmaceuticals (Boston, MA)
    …analytical/organic/physical chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs . Advanced understanding in DMPK, ... ** Program Leadership** **:** + Provides strategic scientific leadership and program management for multiple global CMC development teams dealing with… more
    Takeda Pharmaceuticals (06/27/25)
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  • Principal Biostatistician FSP - Chemistry,…

    Cytel (Cambridge, MA)
    …with cross-functional teams, including analytical scientists, process engineers, and regulatory affairs , to develop and implement appropriate statistical ... experience and had exposure to Chemistry, Manufacturing, and Controls ( CMC ) data analysis. You are excited and enthusiastic, motivate...exciting time to be a part of this new program . **Position Overview:** We are seeking a highly motivated… more
    Cytel (07/18/25)
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  • Associate Director, Clinical Research, Value…

    Takeda Pharmaceuticals (Lexington, MA)
    program management experienced in leading cross-functional clinical programs within Medical Affairs , Clinical Research, Regulatory , CMC or other drug ... phases of development with significant experience within related functions (eg, Medical Affairs , Clinical Operations, Regulatory , CMC , Marketing). + Minimum… more
    Takeda Pharmaceuticals (05/03/25)
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