- System One (Irvine, CA)
- …bonus Overview: Ready to level up your leadership career? Our client, a leading medical device manufacturer, is seeking a hands-on change agent to lead ... role. If you thrive in a collaborative, fast-paced environment focused on innovation, quality , and continuous improvement, this is your chance to make a real impact.… more
- Fujifilm (Sacramento, CA)
- …or processes. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... must have expert level knowledge in all areas of medical informatics, IT infrastructure design and deployment, medical...with MI Project Management (PM) team to deliver high quality Synapse product solutions. + Act as primary technical… more
- Abbott (Alameda, CA)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... where you can grow the career you dream of. + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next… more
- Terumo Neuro (Aliso Viejo, CA)
- …or Scientific field. 2. Minimum six (6) years of relevant work experience in medical device industry. 3. Strong written and verbal communication skills. 4. ... post market phases. Work closely with R&D counterparts, Operations, Quality , and Regulatory in supporting the development of new...and spatial packaging of components. 7. Working knowledge of medical devices and FDA regulations. 8. Experience… more
- Fujifilm (Sacramento, CA)
- …as assigned. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
- J&J Family of Companies (Irvine, CA)
- …__ **Experience** + 2-4 years of experience in project coordination, ideally in medical device , biotech, or pharma R&D. + Exposure to regulated environments ... basic process improvements that lead to improvements in productivity, quality , and cost. + Coordinates development and quality...( FDA , ISO 13485, EU MDR) and understanding of design… more
- J&J Family of Companies (Santa Clara, CA)
- …human factors engineering. + Solid understanding of ISO 14971 and IEC 62304. + Medical Device product development or experience working in a highly regulated ... methods and techniques for evaluations. + Collaborate with R&D, Marketing, Medical Safety, Regulatory Affairs, Clinical Engineering, and Quality Engineering… more
- Abbott (Pleasanton, CA)
- …a global leader in the research, development, manufacturing, sales and marketing of medical device products. The ideal candidate will have experience working ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Fujifilm (Sacramento, CA)
- …and procedures. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... Knowledge Base articles. + Maintains an expert working knowledge of current medical imaging products and related technologies. + Engineers must have the ability… more
- Medtronic (San Francisco, CA)
- …and resolve gaps. + Experience working in a regulated environment--ideally the medical device industry. + Proactively drives results. **Physical Job ... additional overnight or occasional flight travel. + Understands and adheres to FDA Regulations, quality and training requirements, SOPs, and Work… more