- Philips (San Diego, CA)
- …Biomedical Engineering, or a related field. Experience applying IEC 60601-1 and related medical device electronics standards is desirable. + You must be able ... **Senior/Staff Digital Electrical Engineer** **- FPGA for Medical Devices (San Diego, CA)** As a member...verification and validation plans in collaboration with Quality and Regulatory teams, actively participating in transferring designs from R&D… more
- 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. ... designed and manufactured in compliance with applicable industry and regulatory standards and meet customer expectations for safety and...and technical QA staff. * Deep knowledge of global medical device regulations (FDA, EU MDR, etc.).… more
- Abbott (Milpitas, CA)
- …in model based design (UML or SysML), is highly desirable + Detailed experience with medical device development processes and FDA 510K and PMA regulatory ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Stryker (Irvine, CA)
- …Management etc.), and related integrations + Salesforce certification preferred + Medical device or pharmaceutical industry experience preferred + Experience ... such as MS Project, Smartsheet or equivalent + Awareness of regulatory , security, legal, and ethical implications of IT solutions **Education/Experience Preferred**… more
- Gilead Sciences, Inc. (Foster City, CA)
- …BRH solutions, particularly in regulated environments such as pharmaceutical, biotech, or medical device manufacturing. + Experience with SAP S/4HANA and ... deep expertise in SAP BRH & SAP QM module, regulatory compliance (such as GxP and FDA), and life...time off, and a benefits package. Benefits include company-sponsored medical , dental, vision, and life insurance plans*. For additional… more
- Teledyne (Camarillo, CA)
- …development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals ... team to solve material growth and processing issues, and to improve device designs, processing methods, and production capabilities. + Assurance of all production… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... products as subject matter expert on product design, including design changes and regulatory inquiries. + Prototype and develop proof of concept designs and test… more
- Fujifilm (Sacramento, CA)
- …and advertising regulations and other regulations specific to Life Sciences/Pharma and Medical Device companies. + Perform other duties as assigned. **Required ... new business ventures. + Keep abreast of legislative and regulatory changes that may affect HLUS and its subsidiary...and/or in-house legal department, preferably in the Life Sciences/Pharma, Medical Device or health care field. +… more
- Medtronic (Northridge, CA)
- …and cross-functional teams to ensure compliance with ISO 10993 standards and global medical device regulations. The role also supports product development by ... concise, and well-structured test plans and reports to support regulatory submissions. This role involves coordinating required chemical characterization testing,… more
- J&J Family of Companies (Irvine, CA)
- …of J&J MedTech. The ideal candidate is a hands-on technical leader with regulatory and commercial awareness, able to simplify complex security topics to various ... secure communications (eg TLS/mTLS). + Oversee security integration across medical devices, software, mobile applications, embedded devices, and cloud environments… more