• 3D Heterogeneous Integration Design Enablement…

    Global Foundries (Malta, NY)
    …visit www.gf.com . Summary of Role: GlobalFoundries Fab8 is seeking a motivated R&D design enablement engineer to become part of our state-of-the-art 300mm ... (3DHI) design enablement to enable our next-generation advanced packaging R&D efforts, which include wafer - to - wafer...K it) teams to translate packaging requirements to a device enabl e ment specification covering: design rules ,… more
    Global Foundries (07/23/25)
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  • Principal Hardware Test Engineer (LabView…

    Medtronic (Boulder, CO)
    …+ Experience with wireless communication protocols such as WiFi and Bluetooth + Medical Device experience, QSR experience, and familiarity with change control ... **A Day in the Life** The Principal Hardware Test Engineer is a member of the Operations Engineering team....also support interacting with test systems on our Ligasure device lines and the Ultrasonic platform production lines. These… more
    Medtronic (10/01/25)
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  • Sr. Software Engineer - C & Qt

    Capgemini (Waltham, MA)
    Engineer and make a significant impact in developing innovative C based applications for medical devices on Linux OS. This role is ideal for a motivated ... Role: Software Engineer - C Location: Waltham MA - 100%.... Develop modern C (11' or newer) based standalone medical device applications in Linux OS .… more
    Capgemini (09/17/25)
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  • Electrical Engineer 3

    Hologic (Newark, DE)
    …to work independently. + Takes initiative. + Understanding of electronic design, medical device design, analog/digital circuit design, PCB design, software, ... Electrical Engineer 3 Newark, DE, United States **Why Hologic**...an automated cell/line + Experience in an FDA regulated medical device industry is beneficial. + Experience… more
    Hologic (09/17/25)
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  • Field Services Engineer IV

    Medtronic (Los Angeles, CA)
    …or technology field. + Previous experience as Technician/Field Services within medical device industry. + Experience with orthopedic anatomy, surgical ... + Familiar with the FDA 21 CFR, CGMP for Medical devices . + Excellent analytical and communication...to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
    Medtronic (10/08/25)
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  • Senior FPGA Design Engineer

    Medtronic (Newton, MA)
    …the guidance of some of the industry's prominent experts in the field of medical device engineering while working in a fun and collaborative office environment. ... a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. As a Senior Hardware Engineer , you will be… more
    Medtronic (09/10/25)
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  • Senior Supplier Quality Engineer I…

    Integra LifeSciences (Princeton, NJ)
    …in Engineering or associated scientific discipline. + Minimum 5 years Medical Devices or Pharmaceutical experience in Quality or R&D Engineering position. + ... are to: + Support the development and manufacturing of medical devices in conformance with the Quality...in conformance with the Quality System Regulation, ISO 13485, Medical Device Directive, ISO 14971, IEC 60601… more
    Integra LifeSciences (10/02/25)
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  • Sr. Supplier Quality Engineer

    Medtronic (Minneapolis, MN)
    …controls. Utilize GMP (Good Manufacturing Practices) for Class II and Class III medical devices to ensure quality products and outcomes. Navigate the ... regulations to include FDA QSR 21 CFR 820, EU Medical Device Directive (EU MDD 93/42 EEC),...product controls; GMP for Class II and Class III medical devices ; FDA QSR 21 CFR 820,… more
    Medtronic (08/15/25)
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  • Manufacturing Engineer II - Packaging…

    Medtronic (Billerica, MA)
    …own the packaging processes that support the safe handling of life-saving medical devices . You'll collaborate cross-functionally to ensure our packaging meets ... **Nice to Have** **: Preferred Qualifications** + Experience in medical device , pharmaceutical, or other regulated industries....to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
    Medtronic (09/30/25)
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  • Principal Software Engineer - Cloud

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …expertise in applying FDA design control requirements (21 CFR ) as applied to medical device software and medical device regulation (IEC-62304) ... **Job Description** We're looking for a Principal Software Engineer to join our growing team and lead...developers in the delivery of products, both in an R&D and Commercial setting + Estimate engineering effort, plan… more
    Otsuka America Pharmaceutical Inc. (08/08/25)
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