- Abbott (Pleasanton, CA)
- …United States alone, and Abbott's coordinated effort to bring new medical device solutions to this population is revolutionizing how this debilitating condition is ... and financial product performance + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating… more
- Abbott (Sunnyvale, CA)
- …and delivering of custom in-house software/ hardware tools developed for Implantable Device Firmware projects towards meeting both short term and long-term goals of ... request dispositioning, and training. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …data teams at OPH. The ideal candidate will have experience advising medical device , digital health, and AI clients on the application of healthcare regulatory laws ... of OPH healthcare products, services, and technology. Expert knowledge of medical device and consumer protection (eg, FDA, FTC), healthcare compliance (eg, FCA,… more
- Teleflex (San Diego, CA)
- …and services. Teleflex Surgical is creating a world-class culture for surgical device representatives. We stand for excellence in everything we do through personal ... Requirements** * A bachelor's degree or 8+ years of prior B2B or medical device sales experience is expected, with a demonstrated track record of success. * A… more
- J&J Family of Companies (Santa Clara, CA)
- …portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary ... 5 years' experience as an R&D technician (or relevant experience) in the medical device industry or Associate's degree with 3 years' experience in the medical … more
- Fujifilm (Sacramento, CA)
- …by the Manager, Site Planning. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 ... Project Management. + At least 5 years of medical device planning experience is required. + Educational Requirements: +...skills and be self-motivated. + 5 years of medical device planning preferred. + Must have strong computer skills.… more
- AbbVie (Irvine, CA)
- …regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates or Drug Products produced by AbbVie plants or by third-party manufacturers, ... development of global Product Quality Assurance strategy to support pharmaceuticals, biologics, device and combination products produced at AbbVie plants as well as… more
- Abbott (Sylmar, CA)
- …cardioverter defibrillators (ICDs), leads, electronic systems, and related medical device assemblies. Performs routine assignments according to specified and/or ... Locates and corrects problems using microscope and applicable tools; Reviews all device documentation for completeness and accuracy. + Notifies supervisor of the… more
- Abbott (Sylmar, CA)
- …cardioverter defibrillators (ICDs), leads, electronic systems, and related medical device assemblies. Performs routine assignments according to specified and/or ... and corrects problems using microscope and applicable tools; c. Reviews all device documentation for completeness and accuracy. 5. May set-up/utilize special test… more
- GRAIL (Menlo Park, CA)
- …related disciplines is strongly desired. + Experience working on IDE trials and device registries within the medical device and/or pharmaceutical industry. + ... contact us (https://grail.com/about/#contact-us) to request accommodation. GRAIL maintains a drug -free workplace. GRAIL is an Equal Employment Employer and does… more