• Technical Writer - Purchasing

    PCI Pharma Services (Rockford, IL)
    …and subject matter experts (SMEs) to gather and verify technical and regulatory information. + Ensure all documentation complies with internal standards and external ... periodic reviews and updates of existing documentation to reflect process or regulatory changes. **Requirements:** + Minimum 2 years of working in the pharmaceutical… more
    PCI Pharma Services (07/02/25)
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  • Mass Torts Legal Writer (Attorney)

    Launch That (Orlando, FL)
    …in downtown Orlando. We cover 100% of the premium cost for employee-only medical coverage for all full-time team members. We also offer 100% employer-paid short- ... with direct experience in Mass Tort litigation, ideally involving defective drugs, medical devices, or product liability. The ideal candidate has a strong… more
    Launch That (06/25/25)
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  • Associate Scientific Writer

    ThermoFisher Scientific (Middleton, WI)
    …on the guidelines and requirements of the FDA and other international regulatory agencies for reference in the development of required documents. + Mentored/trained ... role._ **Knowledge, Skills, Abilities** + Working knowledge of scientific terminology, medical , pharmaceutical and research concepts + Knowledge of word processing,… more
    ThermoFisher Scientific (08/03/25)
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  • Corporate Communications Content Writer

    ERCOT (Austin, TX)
    …the Public Information Request apparatus, using research and knowledge of regulatory and industry requirements to determine appropriate responses + Explain ERCOT ... equal employment for all qualified persons without regard to race, sex, medical condition, religion, age, creed, national origin, citizenship status, marital status,… more
    ERCOT (07/11/25)
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  • Data Flow & Architecture Documentation Analyst

    ManpowerGroup (Phoenix, AZ)
    Our financial services client is seeking a Technical Writer to join their Regulatory Data & Architecture team. As a Technical Writer , you will be part of the ... order to well-structured documentation. This can be a Technical Writer or Data Analyst or Business Analyst who has...completion of waiting period consultants are eligible for:** + Medical and Prescription Drug Plans + Dental Plan +… more
    ManpowerGroup (06/24/25)
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  • Senior Copywriter

    Cramer (Norwood, MA)
    …you need a strict eye for detail to ensure our work adheres to regulatory , legal, and medical guidelines. Your day-to-day will include researching, creating, ... important audiences. Position Summary: We are seeking a Senior Writer to join our Cramer Health team. As part...direction and work independently-a creative thinker who never forgets regulatory rules-and excited to work closely with internal and… more
    Cramer (06/27/25)
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  • Analyst II, Medical Writing, Immunology

    J&J Family of Companies (Spring House, PA)
    …experience is required. + A minimum of 2 to 4 years of regulatory medical writing experience is required, depending on tasks performed and ... profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical Writing **Job… more
    J&J Family of Companies (07/30/25)
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  • Import/Export Coordinator

    Lineage Logistics (Tacoma, WA)
    Additional Job Description **Remote Customs Entry Writer ** **Schedule:** Monday-Friday | 8:00 AM - 5:00 PM **Location:** Remote (Equipment Provided) We are seeking a ... detail-oriented and experienced **Customs Entry Writer ** to join our team. In this critical role,...+ Stay current on changes in import/export laws and regulatory updates. + Advise clients on tariffs, restrictions, insurance… more
    Lineage Logistics (07/24/25)
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  • QA Technical Writing Management NS &E

    ABBTECH Professional Resources, Inc. (Oak Ridge, TN)
    **Job Summary:** The primary role of the UPF Startup Technical Writer will be to support the Startup team with Test Packages. To ensure technical editing, graphics, ... editorial changes. Provide accurate input to the Startups Lead Technical Writer to prevent delays in testing activities. **Major Responsibilities:** Take detailed… more
    ABBTECH Professional Resources, Inc. (05/15/25)
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  • Future Opportunities- Join Our Talent Pipeline…

    AbbVie (Mettawa, IL)
    …talent pipeline and considered for future opportunities. About the role: The Principal Medical Writer is responsible for providing writing support and advanced ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...required or in a related area such as quality, regulatory , publications, clinical research, or product support/R&D. + 2… more
    AbbVie (07/14/25)
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