- 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 ... - External** Johnson & Johnson is hiring for a **Sr. Manufacturing Engineer, Shockwave Medical ** to join our team located in **Santa Clara, CA** . At Johnson &… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …software + Lead regulatory effort to comply with new and existing regulations (eg, FDA Medical Device Regulations, EU-MDR) + Support the monitoring, ... Develop and implement global regulatory strategy for MMS Dispensing Medical Device and non- Medical ...experience including SaMD/SiMD is a plus + Regulatory and Quality Information Management systems such as SAP, RIM, or… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …to comply with new and existing US and international regulations and directives (eg, FDA Medical Device Regulations, EU Low Voltage Directive, EU ... + Minimum of five (5) years of Regulatory Affairs experience in the medical device industry required + Strong prioritizing, interpersonal, communication, and… 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
- ManpowerGroup (San Diego, CA)
- …of OAuth 2.0, OpenID, TLS, and cybersecurity. **Preferred:** + Experience with medical device regulations (ISO 13485, IEC 62304, FDA 21 CFR Part 820). + ... preferred). + 10+ years of experience in software/system development, preferably in connected device or medical device environments. + Strong Agile… more
- GRAIL (Menlo Park, CA)
- …experience in managing clinical trials at a sponsor company (pharma, biotech, or medical device ) with a strong track record of successful trial initiation ... executed within compliance of regulations and of the highest quality , and to be able to identify areas of...in vitro diagnostics (IVD) highly preferred; pharmaceutical, biologics or medical device experience also acceptable + Thorough… more
- VTI Life Sciences (San Diego, CA)
- …engineers looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to help support ... instruments, and systems for clients in the biotech/pharmaceutical / medical device industry. This field service role...reporting is a plus. + Previous experience in a cGMP/ FDA -regulated manufacturing environment is a plus. + Must be… more
- Stanford Health Care (Palo Alto, CA)
- …Do: . Manage post-operative heart and lung transplant patients and ventricular assist device (VAD) recipients across ICU and step-down units . Serve in three core ... the NP and his/her supervising physician(s), and approved by the appropriate medical and nursing administrators, the IDPC, the Credentials & Privileges Committee,… more
- Medtronic (Los Angeles, CA)
- …Bachelors degree required + 3+ years of service experience, at least 1 year of medical device experience with robotics technologies a plus **Nice to Have** + ... to RAS service activities + Active participation in RAS quality system. Function as a liaison between service team...understand schematics and engineering drawings + Familiar with the FDA 21 CFR, CGMP for Medical devices… more
- Imperative Care (Campbell, CA)
- …or master's degree in engineering with 2 years of related experience in the medical device or related regulated industry; or equivalent combination of education ... to measure and quantify the physical characteristics and performance of the device by experimental design. Your knowledge of solid mechanics, fluid mechanics,… more