- Physics World (Livermore, CA)
- …requirements. Develop and maintain a comprehensive suite of documents to support the IAP data governance strategy, including documentation on data lineage, ... and briefings to senior leadership, stakeholders, and NNSA headquarters in support of data integration initiatives and governance requirements. Develop and implement… more
- DeepHealth (Boston, MA)
- …planning and regulatory requirements for non‑medical devices, and medical device . Leads and manages regulatory submissions, including US 510(k)s submissions, ... and regulatory team members to ensure compliance for and support of OUS regulatory submissions and filings. Monitor and...a regulated industry (FDA and Software as a Medical Device preferred). Strong knowledge of FDA Quality System Regulations,… more
- nEye Systems, Inc. (Santa Clara, CA)
- …full lifecycle of reliability qualification in telecom‑grade environments. Key Responsibilities Support the development and execution of reliability test plans for ... design and optimize reliability test setups, including scripting or automation support . Collect, analyze, and interpret reliability data using statistical techniques… more
- Diligent Consulting Inc (Washington, DC)
- …award. Diligent Consulting Inc. is seeking a Security Monitoring Specialist to support the Government Publishing Office (GPO) as part of its SecDevOps Program ... refining and tuning Zero Trust security monitoring systems to validate user and device trust on an ongoing basis. Key Responsibilities: Monitor and tune ZTA (Zero… more
- Qualcomm (San Diego, CA)
- …of system initialization, secure boot and authentication, platform and device configurations, execution environment enablement across new emerging CPU architectures, ... and non‑volatile memory (UFS, NVMe, eMMC, NAND, SPI‑NOR, etc) device and interfaces (USB, PCIe) initiations and device...addition, our highly competitive benefits package is designed to support your success at work, at home, and at… more
- DeepHealth (Boston, MA)
- …planning and regulatory requirements for non‑medical devices, and medical device . Leads and manages regulatory submissions, including US 510(k)s submissions, ... and regulatory team members to ensure compliance for and support of OUS regulatory submissions and filings. Monitor and...a regulated industry (FDA and Software as a Medical Device preferred) Strong knowledge of FDA Quality System Regulations,… more
- Integral (Honolulu, HI)
- …POM Specialist based in Honolulu, HI. The role entails ensuring mobile device management and supporting end-user needs for a government institution. Candidates ... should have significant experience in IT environments, specifically related to MDM and configuration management. Benefits include comprehensive insurance options and a tailored rewards package. #J-18808-Ljbffr more
- Teradyne (North Reading, MA)
- …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... high-throughput software and electro-mechanical handling solutions to validate semiconductor device performance and determine whether product quality levels have… more
- Northeastern University (Boston, MA)
- …recover under attack. The platforms will also shape the evolution of medical device security regulatory frameworks by moving evaluations from individual device ... Lead and direct research projects in healthcare and medical device cybersecurity. Define research objectives, contribute to requirements engineering, direct… more
- TechDigital Group (New York, NY)
- …standards, meet MISRA guidelines, and follow other best practices Implement ROS support for middleware Support flow of information through configuration and ... (SPI, I2C, CAN, PCIe, MIPI CSI, SERDES, Ethernet, UART) Design and develop FreeRTOS device drivers using C Design and develop Classic AUTOSAR services and Complex … more
