- Abbott (Menlo Park, CA)
- …**Preferred Qualifications** + Professional certification(s) desirable + Experience in the medical device industry + Bachelor's Degree in EHS, engineering, ... Mission: Why We Exist Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for… more
- Abbott (Pleasanton, CA)
- …with cross-functional peers in quality , operation, marketing, clinical and regulatory , medical affairs, commercials to define an aligned and predictable ... time, within budget and with quality . You will work closely...organization. + Minimum of ten (10) years' experience in medical device development and/or other highly regulated… more
- Philips (San Diego, CA)
- …You have a minimum of 8+ years' experience in FDA regulated, IEC 62304 medical device software environments (SiMD/SaMD), with a focus on Software Design ... practices, cutting-edge tools, and innovative methodologies to continuously enhance software quality and regulatory compliance. + Will oversee the development,… 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
- ManpowerGroup (San Diego, CA)
- …preferred). + 10+ years of experience in software/system development, preferably in connected device or medical device environments. + Strong Agile ... understanding of OAuth 2.0, OpenID, TLS, and cybersecurity. **Preferred:** + Experience with medical device regulations (ISO 13485, IEC 62304, FDA 21 CFR Part… 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
- J&J Family of Companies (Irvine, CA)
- …study team; o Cooperates with cross-functional teams (Research & Development, Complaint Handling, Quality / Regulatory , Medical Affairs, Medical Safety) to ... R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs, Regulatory Affairs, Health Economics and.... Clinical/ medical background is a plus. . Medical device experience is highly preferred. REQUIRED… 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...validate robust, scalable test methods aligned with product and regulatory requirements. + Troubleshoot and optimize test setups using… more
- Abbott (Sylmar, CA)
- …diverse and growing portfolio of digital health products, including software as a medical device (SaMD), connected devices, and digital health platforms. This ... with appropriate cross-functional teams and internal and external resources ( regulatory , quality , IT, customers, etc.) to ensure...years of proven experience in Connectivity development within the medical device / life sciences / digital… more
- Abbott (San Diego, CA)
- …(IDEs, debuggers, unit test frameworks) + Knowledge of design controls and regulations for medical device development is a plus + Understanding of quality ... visual modeling, multi-threading, formal development methodologies, and source code management + Medical device product development knowledge is a plus + Ability… more