- Sargent & Lundy (Chicago, IL)
- …technical leadership. Project tasks may include client support on front end design , studies, technical specifications, owner's engineer review and factory ... be responsible for providing engineering expertise related to the design , control, and protection of FACTS devices. You will...of FACTS devices. + As a FACTS Lead Electrical Engineer , you will be responsible for proactively guiding the… more
- Hologic (Newark, DE)
- … medical device software? Hologic is seeking a **Lead Software Design Assurance Engineer ** to play a critical role in driving compliance, innovation, ... Lead Software Design Assurance Engineer Marlborough, MA, United...excellence in software development for both Software as a Medical Device (SaMD) and embedded systems (SiMD).… more
- Insight Global (Golden Valley, MN)
- …in a technical or scientific field *12 years minimum experience a medical device software quality or software design assurance role for finished medical ... Job Description Insight Global is seeking a Principal Design Assurance Engineer to join the...devices. *Comprehensive knowledge on medical software device design standards along with global regulations… more
- Insight Global (Golden Valley, MN)
- …Sr Software Design Assurance Engineer for one of our local medical device clients. This position is responsible for product software quality assurance ... field * 5 years minimum experience with medical device software quality or software design assurance role for finished medical devices. * Comprehensive… more
- Sandia National Laboratories (Albuquerque, NM)
- …RF ICs and Microsystems department (5255) seeks an R&D Microwave and Sensor Engineer to design , fabricate, test, qualify, and deliver custom-designed microwave ... device technologies. + RF or high-speed integrated circuit design using Cadence Virtuoso, Synopsis, or Siemens products. +...law. NNSA Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …Engineering within the medical device industry. + Demonstrated experience with medical device design controls (21 CFR Part 820.30) and risk ... **Job Description Summary** Staff Design Quality Engineer to support product... validation plans and reports. + Ensure compliance with design control procedures, medical device … more
- Actalent (Irvine, CA)
- …by developing risk management plans and reports. Essential Skills + Experience with medical device product development lifecycle, including risk management and ... Job Title: Design Quality Engineer IIJob Description We...TUV, etc.). + Thorough knowledge of US and International Medical Device Regulations. + Strong knowledge of… more
- Actalent (Irvine, CA)
- …and verifying implementation effectiveness. Essential Skills + Experience with the medical device product development lifecycle, including risk management and ... ** Immediate Design Quality Engineer II opportunity **...MoH, TUV. + Thorough understanding of US and International Medical Device Regulations. + Strong knowledge of… more
- Hologic (Newark, DE)
- …States Are you passionate about driving innovation while ensuring compliance and quality in medical device development? At Hologic, we are seeking a **Lead ... Lead Design Assurance Engineer Newark, DE, United...to hear from you! **Knowledge:** + In-depth understanding of medical device regulations and standards, including ISO… more
- Pfizer (Andover, MA)
- …and procedures to support device development and supply. + Support device design and manufacturing investigations from devices used in clinical trials ... device projects. + Support the assessment of external design companies and suppliers for capability of quality systems,...14971, 21 CFR 820, ISO 11040 and the EU Medical Devices Directive. + Working knowledge of EN 62366… more
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