- 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
- 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
- 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
- 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
- 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 (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
- 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
- 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 (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
- 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
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