• Senior Staff Engineer, Modeling

    Takeda Pharmaceuticals (Boston, MA)
    …for a project area/technical program within the department and potentially across Pharmaceutical sciences. + Stay current in novel process modeling and ... 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… more
    Takeda Pharmaceuticals (11/27/25)
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  • Associate Director, IT Compliance & Governance

    Sumitomo Pharma (Boston, MA)
    Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient ... **Job Overview** Lead IT compliance and governance programs in a regulated pharmaceutical environment. Ensure adherence to global regulations (GxP, FDA, EMA), manage… more
    Sumitomo Pharma (01/10/26)
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  • Director, Commercial Drug Products & Life Cycle…

    Amgen (Cambridge, MA)
    …programs for technical activities specific to formulation, aseptic drug product process design and validation , integrated development of combination products, ... process development experience within a major biopharmaceutical or pharmaceutical organization + Demonstrated knowledge of drug product commercialization and… more
    Amgen (12/26/25)
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  • Staff Engineer, Modeling

    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 ... to the best of my knowledge. **Job Description** **OBJECTIVE:** Synthetic Molecule Process Development (SMPD) is responsible for the development of robust and… more
    Takeda Pharmaceuticals (11/28/25)
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  • Manufacturing Process Data Engineer III…

    Sanofi Group (Framingham, MA)
    **Job Title:** **Manufacturing Process Data Engineer III - Biopharmaceuticals** **Location:** Framingham, MA **About the Job** We deliver 4.3 billion healthcare ... function by providing day-to-day Manufacturing Support, focusing on technical and process aspects, effective Life Cycle Management, process robustness… more
    Sanofi Group (01/07/26)
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  • Global Manufacturing Sciences Process

    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 ... drug substance expertise and direct manufacturing experience to support process design, scale-up, technology transfer, and commercial supply. Working… more
    Takeda Pharmaceuticals (12/18/25)
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  • Clinical Lead, Early Clinical and Experimental…

    Sanofi Group (Cambridge, MA)
    …Proof-of-Mechanism/Proof-of-Concept, as well as natural history studies and experimental model validation to contribute building the Human Target Validation ... of multiple disciplines into a coherent translational medicine and human target validation plan is essential. We are an innovative global healthcare company with… more
    Sanofi Group (01/05/26)
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  • Executive Director, Global Clinical Development…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    **Job Summary** Within Otsuka Pharmaceutical Co. exists Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) a USA subsidiary exists the Global ... portfolio evidence generation strategy + Align COA endpoint development and validation work across individual assets + Drive portfolio-wide stakeholder strategy… more
    Otsuka America Pharmaceutical Inc. (01/10/26)
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  • Senior Manager, Benchtop IT Systems - Devens Cell…

    Bristol Myers Squibb (Devens, MA)
    …the Cell Therapy Facility, including requirements gathering, design, implementation, validation , and ongoing support. + Oversee system integration with ... GxP, FDA, and other applicable regulatory standards in system implementation, validation , and operations. + Partner with internal stakeholders (lab users, engineers,… more
    Bristol Myers Squibb (01/20/26)
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  • Director, Quality - Life Sciences

    Datavant (Boston, MA)
    …regulated data services and software. This includes oversight of software validation , privacy compliance, supplier qualification, and audit readiness. You will also ... of quality specialists responsible for core functions such as CAPA, internal audits, validation , and supplier monitoring. + Serve as the primary quality liaison to… more
    Datavant (12/09/25)
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