• Scientist, Manufacturing Science and Technology,…

    BeOne Medicines (Pennington, NJ)
    …unique growth opportunity for professional exposure to many facets of process development and drug substance manufacturing. This position involves close ... troubleshooting, compliance related activities and provide technical support to Drug Substance manufacturing. Process monitoring and trend analysis of manufacturing… more
    BeOne Medicines (12/19/25)
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  • Sr. Manager, Regulatory Affairs Strategy

    Taiho Oncology (Princeton, NJ)
    …directs global regulatory affairs activities and provides regulatory guidance during drug development , approval and post approval processes and ... accessing documentation utilizing multiple electronic systems. + Knowledge of the drug development process, drug laws, global regulations and requirements +… more
    Taiho Oncology (12/13/25)
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  • GMP Manufacturing Technician

    Astrix Technology (Los Angeles, CA)
    …**Why Join?** + Opportunity to work with a dynamic team supporting innovative clinical drug development . + Hands-on experience in a pilot-scale drug ... This role will be based onsite at their pilot-scale drug product manufacturing facility and formulation development ...pilot-scale drug product manufacturing facility and formulation development lab in Thousand Oaks, CA. The technician will… more
    Astrix Technology (10/12/25)
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  • Senior Scientist: Data Analytics…

    Amgen (South San Francisco, CA)
    …on use of data science and predictive analytics methodologies to support drug development via pharmacometric and quantitative systems pharmacology modeling. In ... the pharmacometric modeling to make robust inferences to support clinical drug development across diverse therapeutic areas. **Responsibilities:** + Designs… more
    Amgen (12/20/25)
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  • Team Leader I - Operations Training

    Charles River Laboratories (Ashland, OH)
    …River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities ... and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness… more
    Charles River Laboratories (12/18/25)
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  • Principal Research Scientist - Modeling…

    AbbVie (Irvine, CA)
    …comfortable with exploratory analyses and non-conventional modeling beyond systemic drug development including ophthalmology, and aesthetics/dermatology. This ... correspondences. + Exploratory analyses and non-conventional modeling beyond systemic drug development with a focus on locally-administered/acting products.… more
    AbbVie (12/10/25)
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  • Senior Manager, Global Product Quality - Biologics

    Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
    …and performing root cause analysis. + Thorough understanding of GMP requirements and the Drug Development process. + Knowledge of FDA 21 CFR Parts 210 and ... for Otsuka's patients. **Job Description** + Provides Biologics QA support for Drug Substance and Drug Product, including upstream and downstream biologics… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Research Analyst I - Formulations 1

    Charles River Laboratories (Stilwell, KS)
    …River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities ... and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness… more
    Charles River Laboratories (11/01/25)
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  • Senior Clinical Veterinarian

    Charles River Laboratories (Reno, NV)
    …you will be part of an industry-leading, customer-focused company at the forefront of drug development . Your skills will play a key role in bringing life-saving ... River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities… more
    Charles River Laboratories (11/01/25)
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  • Associate Director, Global Integrated Evidence…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …involved in theIEP, evidencegenerationand governance processes. **Requirements:** + Bachelor's degree in drug development or business management. + 5+ years of ... under pressure, meet deadlines, and lead parallel projects. + Competence in drug development lifecycle and scientific understanding of assets. **Preferred:** +… more
    Otsuka America Pharmaceutical Inc. (12/17/25)
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