- Abbott (Pleasanton, CA)
- …to define and implement comprehensive test automation strategies for Abbott's next-generation medical device software portfolio (Class II and Class III devices). ... including integration and end-to-end testing, to support overall product quality . + Compliance & Quality Assurance...: Ensure all test strategies and practices align with medical device regulatory standards (FDA, ISO, IEC… more
- Medtronic (San Francisco, CA)
- …initiatives. + Report device complaints to proper departments within quality assurance within Medtronic. + Develop and maintain comprehensive clinical ... experience coordinating programs. + Thorough working knowledge of medical terminology, medical procedures and the medical device industry. + Excellent… more
- Teledyne (Camarillo, CA)
- …air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research. ... include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research,… more
- Roche (Carlsbad, CA)
- …Senior Software Engineer (Engineer) will design, develop, and maintain software for a medical device and software tools for internal teams, ensuring compliance ... Engineer will collaborate with cross-functional teams, including hardware engineers, quality assurance , and clinical experts, to define...in software development, at least 3 years in the medical device or healthcare industry. + You… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …new and existing US and international regulations and directives (eg, FDA Medical Device Regulations, EU Low Voltage Directive, EU Electromagnetic Compatibility ... regulatory impact assessments for change controls and other Regulatory Affairs/ Quality Assurance items from a review and...five (5) years of Regulatory Affairs experience in the medical device industry required + Strong prioritizing,… more
- Bausch + Lomb (Sacramento, CA)
- …(eg, R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance , Pharmacovigilance/GPSS and Drug/ Device Safety, ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… more
- Logitech (San Jose, CA)
- …The Principal Software Automation QA Engineer will lead the quality assurance efforts for the Video Conferencing device team, ensuring the end-to-end ... testing automation frameworks and related processes to ensure reliable Quality Assurance platforms. + Test Case Development:...We believe that good health means more than getting medical care when you need it. Logitech supports a… more
- Abbott (San Francisco, CA)
- …case debriefing calls + Providing documentation as required from customer for quality assurance initiatives + Coordinating communication with internal and ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- BeOne Medicines (Emeryville, CA)
- …and Experience: + BA/BS degree required; advanced degree preferred. + GCP Quality Assurance auditor's registration/certification preferred. + Minimum of 7 years ... of experience in GCP-related Quality Assurance function of the pharmaceutical, biotechnology...of international GCP requirements and standards in the pharmaceutical, medical device and biotech industries. + Excellent… more
- Abbott (San Diego, CA)
- …+ Minimum 15 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD ... + Minimum 20 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD… more