• Senior Medical Writer / Senior…

    Abbott (Santa Clara, CA)
    …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives… more
    Abbott (09/26/24)
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  • Technical Writer - Regulatory…

    Cordis (Irvine, CA)
    …of experience in technical writing, preferably in regulatory affairs or the medical device sector. + **Knowledge:** Familiarity with medical device ... **Overview** Cordis is a pioneering medical technology company specializing in groundbreaking solutions for...keep saving lives. MedAlliance (Cordis) are currently seeking a ** Technical Writer ** to join our Regulatory Affairs… more
    Cordis (11/09/24)
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  • Technical Writer II

    Danaher Corporation (Loveland, CO)
    …job include: + Bachelor's degree. + Minimum 2 years of direct work experience as a technical writer , preferably in medical diagnostics, scientific, or a ... Then read on! We are currently hiring for a Technical Writer II to transform complex, highly...you also possess previous experience in: + The Life Sciences/ Medical Device industry. + Structured FrameMaker. +… more
    Danaher Corporation (09/25/24)
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  • Technical Writer $83,000 - $94,000…

    Fluid Components International (San Marcos, CA)
    …only NIST traceable equipment and instrumentation. The Job: FCI is in search of a Technical Writer to join our team. This position will be responsible for ... We Are Looking For: + A detail-oriented and organized Technical Writer that can manage multiple projects...per company specifications. What's in it For You: + Medical , Vision, and Dental + STD, LTD, Basic Life/AD&D… more
    Fluid Components International (09/13/24)
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  • Senior Quality Compliance Specialist…

    Integra LifeSciences (Boston, MA)
    …outcomes and set new standards of care. The Senior Quality Compliance Specialist - Technical Writer will work with Boston quality system leadership and cross ... education and years' experience in QA/Compliance within the Life Sciences Industry, preferably Medical Device Industry. + Working knowledge of medical more
    Integra LifeSciences (11/06/24)
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  • Medical Writer III

    Cardinal Health (Columbus, OH)
    **_What Medical Writing contributes to Cardinal Health_** The Medical Writer is a member of the Medical Segment Clinical Affairs team and is responsible ... Plans and reports required for CE marked devices. The Medical Writer will plan and develop high...develop high-quality clinical documents. Extensive knowledge of the European medical device guidelines/regulations such as MEDDEV and… more
    Cardinal Health (11/21/24)
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  • Instrument Documentation Writer

    Grifols Shared Services North America, Inc (San Diego, CA)
    …of experience writing end-user software or hardware instructions. Experience in the medical device industry and working in a federally regulated environment ... regions. Grifols Diagnostic Solution is seeking an Instrument Documentation Writer in San Diego, CA. This role will be...bodies (FDA, IVDR, EUDR) and the European Union (EU Medical Device Regulation). + Deliver supporting documentation… more
    Grifols Shared Services North America, Inc (11/26/24)
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  • Regulatory Scientific Writer

    Hologic (San Diego, CA)
    Regulatory Scientific Writer San Diego, CA, United States Discover a career with real meaning. One that offers the opportunity to showcase your talents, achieve ... Regulatory Affairs department is looking for a Regulatory Scientific Writer here in San Diego! In this role, you...and post-market performance follow-up (PMPF) documentation determining if the device meets the requirements according to the IVDR. +… more
    Hologic (11/10/24)
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  • Technical Writer Intern

    Cook Medical (West Lafayette, IN)
    …All internships provide hands-on experience with meaningful projects in the Medical Device Manufacturing Industry. Responsibilities + Create training and ... support materials for updated DPRA Screening Form including video training content. + Create process flow diagram (current and future state) and associated procedure and work instructions for Information Security Assessment process. Seeking buy-in from… more
    Cook Medical (10/01/24)
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  • User Experience Writer

    Highmark Health (Columbus, OH)
    …+ 1 year creating digital content in highly regulated industries such as medical - device /healthcare or financial institutions + 1 year with digital technology, ... requested. **EDUCATION** **Required** + Bachelor's Degree in Communications, Journalism, Technical Writing, UX Writing, Human-Computer Interaction Content Design, or… more
    Highmark Health (10/30/24)
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  • Senior Mobile Device Engineer (MDM)

    Mastercard (O'Fallon, MO)
    …innovation and delivers better business results. **Title and Summary** Senior Mobile Device Engineer (MDM) Who is Mastercard? Mastercard is a global technology ... that unlocks priceless possibilities for all. Overview The Mobile Device Services Engineering team is looking for a Senior...enhance end user experience * Be skilled at explaining technical problems clearly * Be a strong, confident, and… more
    Mastercard (11/08/24)
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  • Sr. Scientist, Medical Writing and Product…

    Cardinal Health (Columbus, OH)
    …consultants have provided expertise and guidance to help pharmaceutical, biotechnology, and medical device companies get their products to market. Our regulatory ... company's commitment to quality and responsiveness. + Proactively develop/maintain technical knowledge, remain up to date on current trends...+ Ideally targeting 5+ years of experience as a medical writer preparing regulated documents in the… more
    Cardinal Health (11/22/24)
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  • Document Control

    Actalent (Irvine, CA)
    Technical Writer - Process Improvement Job...experience in technical writing, preferably in the Medical Device field. + Proficiency in MS ... operational processes. + The ideal candidate has experience in technical writing, process improvement, and documentation standards. Responsibilities + Document… more
    Actalent (11/19/24)
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