• USA Technical Writer

    Adecco US, Inc. (Pearl River, NY)
    Adecco Healthcare & Life Sciences is hiring a contract Technical Writer I for our Pharmaceutical partner in Pearl River, NY. The anticipated wage range for this ... State, or local law; and Holiday pay upon meeting eligibility criteria Technical Writer I **Job Duties:** . Responsible for designing, developing, and updating… more
    Adecco US, Inc. (10/18/24)
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  • Change Management Specialist / Technical

    Broadcom (Fort Collins, CO)
    …Broadcom Inc. is seeking a highly motivated Change Management Specialist with additional Technical Writer and Editor experience to join our team. The position ... a timely manner based on business priorities and schedules with varying interruptions. Technical Writing/Editing: The technical writer /editor performs as an… more
    Broadcom (11/01/24)
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  • Specialist Disclosure Medical Writer

    Merck (Columbus, OH)
    …and data sharing with external researchers. The Specialist (Disclosure Medical Writer ) will be primarily responsible for preparing clinical study registration and ... documents (ie, Clinical Study Reports, Protocols, etc.). + Experience in technical or medical writing, familiarity with clinical research documents preferred. +… more
    Merck (11/02/24)
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  • Equipment & Architecture Manager

    Butler America (Grand Prairie, TX)
    …LLC products. He/she supervises, in a project organization, System Lead, Mechanical Lead and Technical Writer in order to ensure the action items are delivered ... daily basis, the project team (system, mechanic and tech writer ). - Ensure the scope of deliverables is well...- Create Equipment & Architecture deliverables; review and approve technical output (documents, drawings) created by the team. -… more
    Butler America (10/14/24)
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  • Associate Director - CMC Regulatory

    Lilly (Philadelphia, PA)
    …+ Develop understanding and working knowledge of Lilly/Avid radiopharmaceutical's manufacturing and analytical procedures and method validations + Review ... technical documents including testing protocols, technical reports,...degree, or PharmD. + Experience in pharmaceutical development and/or manufacturing with 5+ years of CMC regulatory experience or… more
    Lilly (08/24/24)
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