- BD (Becton, Dickinson and Company) (Brea, CA)
- …* Minimum 15 years of progressive experience in Design Quality Assurance within the medical device industry. * At least 6 years of direct management experience. ... that all IPD products are designed and manufactured in compliance with applicable industry and regulatory standards and meet...and technical QA staff. * Deep knowledge of global medical device regulations (FDA, EU MDR, etc.).… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of current global Good ... Japanese arm. + Previous experience of working in the global pharmaceutical and medical device industry. + Experience working with external service providers. +… more
- Medtronic (Los Angeles, CA)
- …our technology transforms lives Ensure complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or ... of resolutions to meet goals and objectives. Understand current and upcoming Medical Device Reporting (MDRs) and EU Vigilance Reporting requirements by… more
- Abbott (Alameda, CA)
- …is located in Alameda, California.** **What you'll do:** + Conduct single or multi-center medical device clinical studies. + Perform study site visits (SQV, SIV, ... of relevant experience in site monitoring. + Experience in conducting medical device and/or _in-vitro_ diagnostics studies preferred. Pharmaceutical background… more
- GE HealthCare (CA)
- …field. + Minimum 5-8 years of technical project management experience in healthcare software or medical device R&D, with a focus on AI or software integration. + ... a fast-growing business in GE HealthCare, is the global leader in ultrasound medical devices and solutions. The portfolio spans the continuum of care to enable… more
- Bausch + Lomb (Sacramento, CA)
- …areas to provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input in the identification, ... global team members, other B&L departments (eg, R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and… more
- Abbott (Sylmar, CA)
- …Quality, Compliance , Engineering, within a regulated environment, such as medical device , diagnostics or pharmaceutical industries, to develop the competence ... and follow-up skills, as well as attention to detail. **Preferred Qualifications** + Medical device experience preferred. + Knowledge of Cybersecurity and Data… more
- Abbott (Temecula, CA)
- …serve people in more than 160 countries. **About Abbott** For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...groups and other Abbott business units. + Responsible for compliance with applicable Corporate and Divisional Policies and procedures.… more
- Astrix Technology (Irvine, CA)
- …Knowledge of FDA regulations (21 CFR 820/803), ISO 13485 + Experience with medical device complaint handling and regulatory reporting (MDR, Vigilance, etc.)This ... work for a global leader dedicated to helping people see brilliantly. The largest device company in the world - with complementary businesses in Surgical and Vision… 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...essential functions. Visually inspect components and final kits for compliance and specifications. Close vision (20 inches or less)… more