• Sr Principal Scientist -Pathologist…

    Genentech (South San Francisco, CA)
    …for the Translational Safety Digital Pathology group. The successful Sr Principal Sci-Pathologist candidate will lead efforts focused on driving applications for ... the efficient, comprehensive, and integrated safety profiling of Genentech drug candidates from the Research stage through marketed products....to pathology and biology + 10+ years of relevant drug development experience and at least 4 years of… more
    Genentech (09/06/25)
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  • Senior Principal Scientist , Project…

    Boehringer Ingelheim (Ridgefield, CT)
    …and execution of nonclinical safety programs to support the development of drug candidates from discovery to market authorization. The incumbent will be highly ... As the primary interface between global project teams and Nonclinical Drug Safety, the incumbent is responsible for developing nonclinical safety strategies… more
    Boehringer Ingelheim (10/09/25)
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  • Principal Scientist

    Mission Support and Test Services (Las Vegas, NV)
    …Thursday. (subject to change). + Pre-placement physical examination, which includes a drug screen, is required. MSTS maintains a substance abuse policy that includes ... random drug testing. + Must possess a valid driver's license....is required by DOE directive to conduct a pre-employment drug test and background review that includes checks of… more
    Mission Support and Test Services (10/14/25)
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  • Senior Principal Scientist

    Bristol Myers Squibb (San Diego, CA)
    …potential treatment of diverse oncology indications. The individual will apply modern drug design principles to solve medicinal chemistry problems relevant to the ... + Previous experience supporting and advancing target protein degradation and/or antibody- drug conjugate programs is preferred. + Demonstrated ability to contribute… more
    Bristol Myers Squibb (10/22/25)
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  • Chemical Development Principal

    Cambrex High Point (Charles City, IA)
    …a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug ... North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
    Cambrex High Point (10/15/25)
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  • Principal Research Scientist I Eng…

    AbbVie (North Chicago, IL)
    …Combination Product Development (DCPD) team provides expertise to enable the development of drug delivery systems for use with AbbVie therapeutic products as well as ... In this role, you will be leading programs in development of robust drug delivery systems at the intersection of engineering and biopharmaceutics, as well as… more
    AbbVie (09/20/25)
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  • Sr Principal Scientist - Global…

    Lilly (Indianapolis, IN)
    …the world. **Position Brand Description:** Provides technical leadership for drug product manufacturing processes under development and in commercial production ... and applicable functional areas to commercialize new dry oral solid drug products + Leverage prior experience to anticipate commercial manufacturing challenges… more
    Lilly (08/17/25)
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  • Talent Pipeline- Principal Scientist

    Cambrex High Point (Durham, NC)
    …a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug ... North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
    Cambrex High Point (08/13/25)
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  • Principal Scientist (Formulation…

    AbbVie (North Chicago, IL)
    …years' experience as a functional area lead managing small molecule oral solid drug product development. Of experience required, must have 5 years: + leading ... 2 years' experience as a functional area lead managing small molecule oral solid drug product development. Of experience required, must have 2 years of (i), (ii),… more
    AbbVie (10/16/25)
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  • Associate Principal Scientist

    Merck (Rahway, NJ)
    …statistical programming activities for multiple and/or late stage drug /vaccine clinical development projects. Accountability predominantly includes the development ... coordinating the activities of a programming team. + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level… more
    Merck (09/30/25)
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