• Manager, CMC Regulatory

    Lilly (Philadelphia, PA)
    …development and/or manufacturing with a minimum of two years of CMC regulatory experience or related (eg CMC writer ) **Additional Skills/Preferences:** + ... through philanthropy and volunteerism. **Position Overview:** The Manager, Manager- CMC Regulatory is responsible for the preparation and delivery of high-quality… more
    Lilly (08/14/25)
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  • Microbiologist/Technical Writer - Temporary

    Zimmer Biomet (Englewood, CO)
    …seeking a detail-oriented and scientifically driven Microbiologist - Technical Writer to support technical documentation needs across our microbiology, validation, ... and scientifically accurate documentation for medical device development, validation, and regulatory submissions. This is a temporary hourly position and can be… more
    Zimmer Biomet (08/21/25)
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  • Medical Writer

    Astrix Technology (Monmouth County, NJ)
    **Medical Writer ** Clinical Monmouth County , NJ, US Pay Rate Low: 50 | Pay Rate High: 100 + Added - 02/06/2025 Apply for Job At Astrix, we're expanding our team to ... and benefit-risk assessment reports + Ensure all documents are compliant with regulatory guidelines (ICH, EMA, FDA, etc.), internal SOPs, and quality standards. +… more
    Astrix Technology (08/11/25)
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  • Technical Writer /Editor- Contracts

    Red Gate Group (Arlington, VA)
    …impact on defense policy? The Red Gate Group is seeking a Technical Writer /Editor to support the Acquisition Policy & Innovation (API) Directorate within the Office ... Research statutes and the origin of procurement regulations, draft and edit regulatory text and Federal Register notices, and develop economic cost/benefit analyses… more
    Red Gate Group (09/01/25)
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  • CSV Technical Writer

    Capgemini (Titusville, NJ)
    …reports + Collaborate with cross-functional teams including Quality, Engineering, Regulatory , and Manufacturing to gather source material and ensure accuracy ... documentation aligns with FDA, EMA, ICH, and other relevant regulatory standards + Support audits and inspections by preparing...bring:** + 3-5+ years of experience as a Technical Writer in the pharmaceutical or life sciences industry +… more
    Capgemini (08/30/25)
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  • Sr Scientific Writer

    Houston Methodist (Houston, TX)
    At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor for junior staff with an extensive knowledge of both medical and ... ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills to… more
    Houston Methodist (08/23/25)
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  • UX Content Writer

    KeyBank (OH)
    …Street, Suite 1100 - New York, New York 10003 **About the Role** As a UX Writer , you will be a key contributor within the Client Experience Design group of the ... cross-functional teams, and balance user needs with business objectives and regulatory requirements. **Key Responsibilities** CONTENT STRATEGY & DESIGN + Create… more
    KeyBank (09/06/25)
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  • Quality Specialist / Technical Writer

    Teledyne (Billerica, MA)
    …\#TeledyneFLIRDefenseJobs **Job Summary:** The Quality Specialist / Technical Writer will manage Quality documentation, including Standard Operating Procedures ... + Support internal and external audits, ensuring compliance with regulatory requirements. + Support quality governance initiatives, including management reviews… more
    Teledyne (09/06/25)
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  • Associate Customs Entry Writer

    CH Robinson (Laredo, TX)
    CH Robinson is seeking an **Associate Customs Entry Writer ** to join our Global Forwarding division. As a key player on our customs team, you'll navigate the ... skills, master the art of precise data management, and deepen your regulatory knowledge. If you are organized, possess exceptional communication abilities, and… more
    CH Robinson (09/06/25)
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  • Senior Technical Writer

    Actalent (Santa Clara, CA)
    Job Title: Technical Writer Job Description Collaborate with various teams to capture technical information and transcribe it into clear documentation for internal ... design change orders. + Provide oversight on proper documentation for regulatory submissions. Essential Skills + Medical device experience and understanding of… more
    Actalent (08/28/25)
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