• Associate Director, Omnichannel Data Scientist

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …objectives to business partners. + Partnering with end-to-end with business process owners, technical solution owners, engineers, and analysts to understand ... Profound grasp of Machine Learning lifecycle - feature engineering, training, validation , scaling, deployment, scoring, monitoring, and feedback loop. + Have… more
    Otsuka America Pharmaceutical Inc. (05/16/25)
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  • ICT Program Manager - Temp

    Chiesi (Boston, MA)
    …care and consumer-facing self-care). We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social ... many other enriching diversities. Chiesi USA Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent… more
    Chiesi (05/13/25)
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  • Director, US Product Experience - Digital Products

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …align with our growth strategy and patient outcomes. + Build a rapid validation approach with learning/feedback cycles that enable quick iteration. + Initiate POC ... Develop a baseline for POC cycle time to create a repeatable innovation process that shortens the POC cycle time for design, development, evaluation, and investment… more
    Otsuka America Pharmaceutical Inc. (05/13/25)
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  • Director, Clinical Trial Reporting

    Takeda Pharmaceuticals (Boston, MA)
    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 ... Clinical Data Operations & Standards. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led… more
    Takeda Pharmaceuticals (05/19/25)
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  • Quality Manager

    Actalent (North Billerica, MA)
    …and approve regulatory CMC submissions. + Collaborate on drug development, process control, and analytical method development and qualification. Essential Skills + ... Strong knowledge of CMC processes and technical transfer. + Experience in validation , quality assurance, and regulatory practices. + Ability to author CMC regulatory… more
    Actalent (05/19/25)
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  • Quality Manager

    Actalent (North Billerica, MA)
    …projects, initiatives, and actions. + Develop and qualify drug development, process control, and analytical methods. + Ensure quality assurance and compliance ... develop strategic plans. Essential Skills + Experience with CMC, tech transfer, validation , and quality assurance. + Proficiency in regulatory processes, SOPs, GMP,… more
    Actalent (05/15/25)
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  • Project Manager

    Norstella (Boston, MA)
    …our customers come from over 3000 of the world's leading pharmaceutical , contract research organizations (CROs), medical technology, biotechnology and healthcare ... to be a part of Norstella, an organization that consists of market-leading pharmaceutical solutions providers united under one goal: to improve patient access to… more
    Norstella (05/10/25)
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  • Senior Director, Clinical Trial Configuration

    Takeda Pharmaceuticals (Boston, MA)
    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 ... Clinical Data Operations & Standards. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led… more
    Takeda Pharmaceuticals (05/03/25)
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  • In Silico First Program and Strategy Manager

    Takeda Pharmaceuticals (Boston, MA)
    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 ... therapies to patients worldwide. As an integral part of the Pharmaceutical Sciences Sustainability and Technology (PSST) Sustainable CMC & Innovation team… more
    Takeda Pharmaceuticals (04/16/25)
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  • Quality Manager for High Complexity CLIA Lab

    Nanobiosym, Inc. (Cambridge, MA)
    …audit readiness by overseeing and managing clinical lab audits with regulators, pharmaceutical partners, and with other agencies, ensuring that internal system and ... process audits are scheduled and conducted. * Lead and...Ensure the timely and compliant generation of clinical and validation data required to support regulatory submissions for all… more
    Nanobiosym, Inc. (03/06/25)
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