• Clinical Marketing Specialist - Remote

    Stryker (Dallas, TX)
    …and sales materials. You'll also collaborate with cross-functional teams, contribute to product development initiatives, and build strong relationships with EMS ... written materials. + Provide expert clinical input to new product development projects and business development...lab, EP lab or EMS (ALS paramedic) OR Corporate ( medical device marketing, sales, training, or clinical… more
    Stryker (09/19/25)
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  • Project Manager

    Teleflex (Morrisville, NC)
    …Project Management team and is responsible for the execution of assigned New Product Development and Sustaining lifecycle management projects. This may include ... the management of new product development efforts and cost improvement initiatives...project or program management working in a technical discipline, medical device and/or engineering preferred. * Proficiency… more
    Teleflex (07/22/25)
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  • Manager, US Customer Service & Sales Operations,…

    Abbott (St. Paul, MN)
    …customer complaints in compliance with FDA regulations is essential in the medical device industry. + Performance Management and Metrics: Defining, setting, ... policies and procedures. + Collaboration: Working closely with sales, marketing, R&D, product development , logistics, and regulatory teams to ensure seamless… more
    Abbott (09/13/25)
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  • Senior Manufacturing Engineer

    Abbott (Minnetonka, MN)
    …build and debug of tooling, machinery and test equipment + Work with Product Development to ensure Design for Manufacturability + Be innovative, resourceful, ... experience required + Minimum 5 years manufacturing engineering experience. Prior medical device manufacturing engineering experience is preferred, but not… more
    Abbott (09/13/25)
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  • Sr. Manufacturing Engineer (NPI) - Shockwave

    J&J Family of Companies (Santa Clara, CA)
    Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... using DMAIC methodology. + Lead and/or actively participate in process/ product continuous improvement projects (in cooperation with development...+ Minimum five (5) years of experience in a medical device environment or 3 years of… more
    J&J Family of Companies (09/17/25)
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  • Postmarket Surveillance Manager

    BioFire Diagnostics, LLC. (Salt Lake City, UT)
    …or other Scientific Fields) with 6 years of experience in a regulated medical device /IVD industry employment position such as post-market surveillance, quality ... assurance, regulatory affairs, clinical affairs or product development + OR + Masters Degree...Scientific Fields) with 4years of experience in a regulated medical device /IVD industry employment position such as… more
    BioFire Diagnostics, LLC. (09/03/25)
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  • Senior Principal, Regulatory Affairs - Companion…

    Danaher Corporation (Deer Park, IL)
    …with global regulatory agencies, and steering regulatory strategy for new product development and strategic initiatives. By guiding regulatory activities, ... products, including 510(k) and PMA submissions. + Proven track record supporting new product development and complex clinical trials, including IDE approvals and… more
    Danaher Corporation (07/09/25)
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  • Senior Embedded Software Developer, Advanced…

    Amazon (Sunnyvale, CA)
    …technologies and products in the robotics field and other innovative "zero to one" product concepts. Our team has a proven track record of bringing V0 devices to ... the beginning of our ambitions in the consumer robotics and smart device space. We're developing next-generation devices that combine advanced mobility systems,… more
    Amazon (09/11/25)
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  • Director Of Operations

    Actalent (Minneapolis, MN)
    …We're looking for a leader who has successfully scaled operations in a medical device environment-someone who understands what it takes to grow from ... poised for global impact. Skills Continuous improvement, Operations management, medical device , Manufacturing engineering, Lean manufacturing, Process… more
    Actalent (09/09/25)
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  • Document Control Manager

    Fujifilm (Santa Ana, CA)
    …ISO 14971, Brazilian GMPs, Health Canada MDR, Australian Medical Device regulations and regulatory requirements for product registrations where products ... **A minimum of five (5) years of Quality Assurance and or Document Control in a medical device manufacturer or equivalent.** + **A minimum of four (4) years of… more
    Fujifilm (09/06/25)
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