• Staff Engineer, VLSI Design Engineering(Logic…

    SanDisk (Milpitas, CA)
    …+ Participating in Post-Si evaluation and debug + Drive cross function support for productization + Technical guidance and mentoring of junior engineers ... experience + Experience with chip level integration, chip lead, and full product life cycle (requirements, design, implementation, test) of Logic design + Working… more
    SanDisk (09/10/25)
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  • Senior Portfolio Manager

    Stryker (Portage, MI)
    …6 years of professional work experience required Preferred: + 3 years medical device marketing/sales experience preferred + Previous experience in ... you will lead strategic direction for our Transport A&D (Accessories & Disposables) product line- critical solutions that support emergency care teams in the… more
    Stryker (07/03/25)
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  • Quality Technician II

    Jabil (Hendersonville, NC)
    …play a key role in ensuring product quality and compliance within a medical manufacturing environment. You will support Quality Inspectors during product ... + 3+ years of experience in a regulated manufacturing environment, preferably in medical device or pharmaceutical production. + Experience with cGMP, ISO 13485,… more
    Jabil (09/18/25)
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  • Quality Engineer

    Abbott (Houston, TX)
    …statistical/data analysis and report writing skills. + Prior medical device experience preferred. Experience implementing various product and process ... ensure appropriate environmental monitoring and that microbiology requirements are considered in product and process development activities + Support all Company… more
    Abbott (09/04/25)
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  • Quality Engineer II

    Fujifilm (Bothell, WA)
    …least 2-4 years of experience working within the Quality organization of a Medical Device Manufacturer, Aerospace, Pharma, or other highly regulated industry. + ... and prevention. + Participate in Configuration Management initiatives. + Support new product development in ensuring compliance...the top of the salary range)._ + Insurance: + Medical , Dental & Vision + Life & Company paid… more
    Fujifilm (09/24/25)
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  • Principal Strategic Sourcing Specialist

    Medtronic (Billerica, MA)
    …to achieve results across a matrixed and virtual organization + Experience in the medical device industry with knowledge of applicable FDA/GMP and International ... work together to engineer the extraordinary. Provide operations sourcing support for the disposables and capital product ...medical device regulations and standards **Physical Job… more
    Medtronic (09/28/25)
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  • Operational Excellence Co-Op

    J&J Family of Companies (Anasco, PR)
    …Excellence (OpEX) Department to improve efficiency in a high volume medical device production environment, increase process capabilities, improve process, ... direct hire roles. Expert leaders mentor student contributions and support their technical and professional development during coop/internships. In...Power BI is a plus. + Previous Experience in Medical Device , Pharma or Biomedical Industry. +… more
    J&J Family of Companies (09/27/25)
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  • Aseptic Process Technician/Operator (GMP)

    Mentor Technical Group (Monroe, NC)
    …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... aseptic/sterile manufacturing experience in a GMP-regulated facility (pharmaceutical, biotech, or medical device ). + Knowledge: + Strong understanding of aseptic… more
    Mentor Technical Group (09/10/25)
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  • Quality Information Systems Manager (Days 8am…

    LSI Solutions (Victor, NY)
    …in 1986, located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive ... passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R)...regularly updated as to goals, progress, and challenges. + Support Quality and Regulatory implementations of information systems for… more
    LSI Solutions (09/25/25)
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  • Staff Clinical Compliance Auditor

    Danaher Corporation (Minneapolis, MN)
    …include: + Bachelor's degree with 6+ years clinical quality experience within diagnostics or medical device industry, or Master's or Doctoral degree with 4 years ... understanding of ISO 14155, 13485, 14971, 20916, in vitro diagnostic regulation (IVDR), medical device regulation (MDR), and pertinent sections of 21 CFR. +… more
    Danaher Corporation (09/19/25)
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