• Manager, Labeling Technology

    BD (Becton, Dickinson and Company) (Covington, GA)
    …and cross-functional collaboration. + Knowledge and understanding of FDA and ISO medical device development regulations; especially as they pertain ... to design control and product development . Including knowledge of barcode standards and compliance requirements...highly desired. + Prior knowledge of medical device packaging, labeling, labeling management software , UDI… more
    BD (Becton, Dickinson and Company) (07/09/25)
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  • Senior Clinical Engineer - Monarch Urology

    J&J Family of Companies (Santa Clara, CA)
    …A.) Undergraduate degree with a minimum of 5 years of related work experience in medical device industry OR B.) Master's with 4 years of related work experience ... humanity. Learn more at https://www.jnj.com **Job Function:** R&D Product Development **Job Sub** **Function:** Biomedical Engineering **Job Category:** Scientific/Technology...in medical device industry OR C.) a PhD… more
    J&J Family of Companies (09/10/25)
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  • Senior Manager, Project Leadership

    Abbott (Alameda, CA)
    …of education and work experience + Minimum 10 years of related work experience with medical device product development + Has successfully led several high ... full life. You'll also have access to: + Career development with an international company where you can grow...+ Experience designing and implementing design control tools within medical device industry. + Require strong technical… more
    Abbott (07/29/25)
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  • Sr. Scientist, Multi-Discipline

    Corning Incorporated (Corning, NY)
    …system integration + Demonstrated ability to integrate hardware, electronics, and software in device /system prototyping + Experience with experimental planning, ... and engineers to deliver breakthrough solutions and accelerate the development of next-generation products and processes. Projects span cutting-edge...mechanical assembly, device fabrication, and laboratory test setups + Technical expertise… more
    Corning Incorporated (08/13/25)
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  • Director, Quality Assurance

    Cook Medical (West Lafayette, IN)
    …discipline, Masters or PhD preferred;* 10+ years QA experience working in the medical device , biotechnology, or pharmaceutical industry;* 5+ years in leadership ... outputs and to improve the CRMS;* Provide vision, direction, development , and leadership to the Quality Assurance Team in...integrate and support the goals and direction of Cook Medical ;* Be knowledgeable of and stay current on regulations… more
    Cook Medical (08/29/25)
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  • Intern, R&D Undergraduate Summer - Titans SW,…

    Sandia National Laboratories (Albuquerque, NM)
    …our TITANS Software interns work on include: + Collaborate on Cutting-Edge Software Development : Engage in the design, development , and optimization of ... national security mission. Projects are primarily focused on the development and innovation of software solutions. Successful...law. NNSA Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as… more
    Sandia National Laboratories (09/13/25)
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  • Lead Test Automation Architect (Cloud, Web,…

    Abbott (Pleasanton, CA)
    …to define and implement comprehensive test automation strategies for Abbott's next-generation medical device software portfolio (Class II and Class ... full life. You'll also have access to: + Career development with an international company where you can grow...Assurance: Ensure all test strategies and practices align with medical device regulatory standards (FDA, ISO, IEC… more
    Abbott (07/16/25)
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  • Quality Assurance Engineer 2

    Teleflex (Coventry, CT)
    …leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades ... is preferred or 3+ years of Quality Assurance experience working in the medical device manufacturing environment (a combination of education and experience will… more
    Teleflex (09/05/25)
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  • Lead Test Engineer

    Abbott (Alameda, CA)
    …Excellent knowledge of general Engineering principles. + Extensive Knowledge of regulations for medical device development (ISO134851, ISO13485, FDA) is a ... in the area of electrical engineering, manufacturing processes, and/or software development . Helps drive the design and...+ Extensive knowledge and understanding of GxP, ISO and medical device regulations and the development more
    Abbott (06/25/25)
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  • Principal Regulatory Affairs Specialist - Vascular…

    Abbott (St. Paul, MN)
    …necessary detail. + Maintains ongoing surveillance and analysis of all pertinent medical device regulations to ensure submission requirements worldwide are ... full life. You'll also have access to: + Career development with an international company where you can grow...device regulations, or with EU and other international medical device regulations and submissions. + Must… more
    Abbott (08/23/25)
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