• New Product Introduction Engineer 2

    Cook Medical (Bloomington, IN)
    …or Engineering Technology- Minimum of 3 years experience working in Class II/III medical device manufacturing environment with qualification of new processes and ... Overview The New Product Introduction (NPI) Engineer will bridge Product Development into...manufacturing, statistics and lean manufacturing principles - Knowledge of medical device quality standards ISO13485/FDA practices,GMP and… more
    Cook Medical (09/12/25)
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  • New Product Introduction Engineer 1

    Cook Medical (Bloomington, IN)
    …in Engineering, or Engineering Technology- Experience working in a Class II/III medical device manufacturing environment, with qualification of new processes and ... Overview The New Product Introduction (NPI) Engineer 1 will bridge Product Development ...manufacturing, statistics, and lean manufacturing principles - Knowledge of medical device quality standards ISO13485/FDA practices, GMP,… more
    Cook Medical (09/12/25)
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  • Staff Electrical Engineer

    TE Connectivity (Wilsonville, OR)
    …field. * Experience: Relevant work experience, with a preference for experience in medical device development . * Electrical Expertise: In-depth knowledge of ... STAFF ELECTRICAL ENGINEER **At TE, you will unleash your potential...a leader in engineering design and manufacturing within the medical device industry. Specializing in critical components… more
    TE Connectivity (07/26/25)
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  • Staff Software Design Quality Engineer

    Stryker (Fort Wayne, IN)
    …Assurance** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a Medical Device (SiMD) ... Digital Health projects as a software design quality assurance engineer for pre-market new product development projects....4 years of professional experience in the highly regulated medical device industry, with a focus in… more
    Stryker (08/29/25)
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  • Quality Assurance Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device ... of quality programs and policies that ensure that the development , manufacture and distribution of medical products...and Drug Administration (FDA) regulations, ISO 9001, ISO 13485, Medical Device Directive (MOD), the Canadian … more
    Integra LifeSciences (08/17/25)
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  • Senior Embedded Software Engineer

    Abbott (Alameda, CA)
    … is required. **Preferred Qualifications** + Solid knowledge of regulations for medical device development , (EN460001, ISO13485, FDA) is desirable. ... levels with our new sensing technology. This Embedded Software Engineer works independently on the design, development ,...Embedded UI design experience preferred + Detailed experience with medical device development processes and… more
    Abbott (09/06/25)
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  • Software Development Engineer

    Amazon (Sunnyvale, CA)
    …including the Fire TV family of devices. This position is for a seasoned Software Development Engineer in the Wi-Fi SW connectivity organization. You can be part ... startup like environment. Key job responsibilities As a Software Development Engineer - Connectivity, you will work...and protocol analyzers . Experience with Android and Linux development on kernel, device drivers, and frameworks… more
    Amazon (07/20/25)
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  • Medical Devices Software Quality…

    US Tech Solutions (San Bruno, CA)
    …experience in standalone software development , with a solid understanding of medical device software standards such as IEC 62304. **Software Quality ... ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1....Device Software Experience:** 1. Proven experience in software development for medical devices, specifically focusing on… more
    US Tech Solutions (07/18/25)
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  • Senior Engineer Supplier Development

    Abbott (Pleasanton, CA)
    …10-20%, including internationally. **Preferred Qualifications** + Advanced degree. + Prior medical device experience. + Demonstrated supervisory experience. + ... people to restore their health and get on with their lives. Supplier Development Quality Engineer responsible for activities related to supplier selection and… more
    Abbott (09/12/25)
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  • Software Validation Engineer

    Harmac Medical Products (Buffalo, NY)
    …validation. + Minimum 1-3 years working in a manufacturing environment in the medical device industry is preferred. Safety Responsibilities + Following all ... Software Validation Engineer About the Organization Harmac Medical ...Knowledge + Understands regulated type industries + Knowledge of medical device manufacturers and suppliers knowledge preferred.… more
    Harmac Medical Products (07/24/25)
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