- BD (Becton, Dickinson and Company) (San Diego, CA)
- …etc.) + Develop and implement global regulatory strategy for MMS Dispensing Medical Device and non-Medical device products and software + Lead regulatory effort ... to comply with new and existing regulations (eg, FDA Medical Device Regulations, EU-MDR) + Support the monitoring, interpreting, and implementing of current and new… more
- Grifols Shared Services North America, Inc (San Diego, CA)
- …with Current Good Manufacturing Practices (cGMP) + Maintains detailed and accurate device history records and log books using Good Documentation Practices (GDP) + ... Completes and forwards device history records for review in a timely manner...new process transfers + Recommends improvements and revisions to device master records & Standard Operating Procedures (SOPs) **Additional… more
- Cordis (Irvine, CA)
- …the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery ... with regulatory requirements, standards, and guidelines relevant to the medical device industry and ensure that manufacturing processes adhere to these regulations.… more
- TEKsystems (San Diego, CA)
- Job Posting: Test Engineer II - Advanced Medical Device Testing Location: San Diego, CA Industry: Medical Technology / Device Engineering Overview: Join a ... dynamic and innovative team at the forefront of medical device development. We're seeking a Test Engineer II to lead complex testing efforts that support the… more
- Caldera Medical (Westlake Village, CA)
- …requirements. * Ensure timely and accurate complaint evaluations, including medical device reporting (MDR) or equivalent regulatory submissions. * Collaborate with ... * Bachelor's degree preferred. * Experience working within medical device industry and familiarity with 21 CFR 820, and...Caldera Medical? Caldera Medical is a growth stage medical device company dedicated to improving the quality of life… more
- Kelly Services (Irvine, CA)
- …5 years of experience in a Quality, Manufacturing or Engineering function in medical device industry * At least 5 years of experience in a Quality, Manufacturing or ... Engineering function in medical device industry * Experience with MDSAP Audits, health authorities...authorities and notified bodies * Working knowledge of medical device regulations and standards: 21 CFR Part 820 QSR,… more
- Applied Materials (Santa Clara, CA)
- …Responsibilities:** + Work closely with partners and customers to implement new device structures and optimize process integration for device performance. + ... effectively in CMOS Fabs to troubleshoot process integration issues based on device performance + Solve complex problems; using sophisticated analytical thought and… more
- ZOLL Medical Corporation (San Bernardino, CA)
- …(Heart Failure Management system) is a non-invasive, patch-based device that monitors pulmonary fluid levels and has been ... experience in a strong BTB environment, pharmaceutical or medical device field required or + A minimum of two...field clinical support experience for a pharmaceutical or medical device company required or + A minimum of two… more
- NVIDIA (Santa Clara, CA)
- …including BMC-BIOS communication, thermal management, power management, firmware update, device monitoring, firmware security, etc. + Board Bring-up expertise with ... hands-on experience in Device drivers like I2C/I3C, SPI, PCIe, SMBus, Mail-box etc. as well as the device trees for uboot and Linux kernel. + Understanding on… more
- Terumo Neuro (Aliso Viejo, CA)
- …Description:** Support and lead teams in the development of medical device products, including writing or verifying specifications; maintaining product process; ... Material Science Engineering. 2. Ten (10) to twelve (12) years of medical device industry experience. 3. Strong written and verbal communication skills. 4. Ability… more