• Instructor for Master of Science (MS)…

    University of Maryland, Baltimore (Baltimore, MD)
    … affairs aspects, as well deep knowledge in another aspect (eg clinical research ). Drug and biologics development and assessment. *_REQUIRED SKILLS, KNOWLEDGE ... fulfill the faculty position of Instructor (non-tenure track) for the MS in Regulatory Science within the Department of Pharmaceutical Sciences. The MS in … more
    University of Maryland, Baltimore (01/13/26)
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  • Vice President, Regulatory Affairs…

    Sumitomo Pharma (Montgomery, AL)
    …a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For ... HTA submissions. The individual will be responsible for leading development of all non-clinical and clinical regulatory ...the Marketing Brand Teams, Legal, Medical Affairs and Clinical Research in the development of advertising and… more
    Sumitomo Pharma (12/23/25)
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  • Sr. HW Regulatory Compliance Engineer

    Amazon (Sunnyvale, CA)
    Description Amazon Lab126 is an inventive research and development company that designs and engineers high-profile consumer electronics. Lab126 began in 2004 as ... role will include solving ambitious and complex compliance challenges through research , engagement with regulatory agencies, hands-on testing, debugging, and… more
    Amazon (01/13/26)
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  • Sr. Specialist, Regulatory Affairs, Product…

    West Pharmaceutical Services (Exton, PA)
    …**Work Experience** + Bachelor's with 5+ years required; or + Master's degree/ PhD 2+ years medical device regulatory experience required **Preferred Knowledge, ... involves sitting most of the time. **Additional Requirements** + Ability to research , read, analyze, and interpret regulatory literature and documentation,… more
    West Pharmaceutical Services (01/09/26)
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  • Principal Research Scientist I, Lipid…

    AbbVie (San Diego, CA)
    …to a small group of research associates. + Contribute to formulations/process development sections of regulatory filings (IND, NDA etc.) + Review scientific ... novel formulation technologies. + Experience in contributing to formulation and pharmaceutical development sections of regulatory filings is highly desirable. +… more
    AbbVie (01/10/26)
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  • Senior Research Scientist - Functional…

    New York Genome Center (New York, NY)
    …affiliated investigators. The successful candidate will work within NYGC's technology development and collaborative research ecosystem to translate innovative ... and execute complex experiments supporting collaborative projects, internally driven technology development , and grant-funded research . + Analyze, interpret, and… more
    New York Genome Center (01/10/26)
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  • Assistant Director Compliance…

    Brown University (Providence, RI)
    …Recruiting Start Date: 2025-11-11 Job Posting Title: Assistant Director Compliance and Regulatory Services Department: Office of Research Integrity Grade: Grade ... Description: About Brown Brown University (https://www.brown.edu/about) is a leading research university distinct for its student-centered learning and deep sense… more
    Brown University (11/21/25)
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  • Principal Research Scientist I, Biologics…

    AbbVie (North Chicago, IL)
    …teams and will have strong collaborations with several stakeholders, including discovery research , analytical research and development , bioprocess ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Summary: Biologics Drug Product Development (Bio DPD), a part of Development Sciences within… more
    AbbVie (01/15/26)
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  • Head of Research & Development

    Roche (Carlsbad, CA)
    …Genmark including, engineering design and scale-up processes. You will also ensure development processes comply with regulatory requirements to minimize risk to ... of process development procedures and practices to ensure compliance with regulatory , legal and good manufacturing procedures to meet corporate goals. You will… more
    Roche (01/15/26)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Princeton, NJ)
    …scientific background, PhD ., MD, PharmD, MS + Significant experience in regulatory affairs and diagnostic-related development eg, >8-10 years. + Scientific & ... risk mitigation planning. + Cultivate inclusive, high-impact collaboration with Precision Medicine, Research teams, Global and Regional Regulatory Leads, Global … more
    Bristol Myers Squibb (01/19/26)
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