- Abbott (Alameda, CA)
- …development is required. **Preferred Qualifications** + Solid knowledge of regulations for medical device development, (EN460001, ISO13485, FDA) is desirable. + ... preferred + Embedded UI design experience preferred + Detailed experience with medical device development processes and FDA 510K and PMA regulatory requirement… more
- Abbott (Alameda, CA)
- …+ Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device . + Advanced medical knowledge related to common medical ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Abbott (Santa Clara, CA)
- …to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are ... Supports all business segment initiatives as identified by divisional management and in support of Quality Management ...device regulations or with EU and other international medical device regulations and submissions. + Ability… more
- Medtronic (Los Angeles, CA)
- …Certifying Body and/or Notified Body audits/inspections + Experience or training in project management + Experience with medical device industry Regulations, ... business is growing significantly as the market demands reliable medical devices which look and feel more like consumer...+ Conduct quality reviews of Change Orders for Quality Management System documents and records. + Provides expertise and… 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 ... **Requirements** + Bachelor's degree and 10+ years of quality related experience in the Medical Device industry + Excellent working knowledge of current USA Food… more
- Abbott (Alameda, CA)
- …role will ensure the Medical Events Group (MEG) is compliant with global medical device reporting regulations. This position will be based out of our Abbott ... reporting process. + Responsible for identifying any trends that are found during the medical event process and alerting management in a timely manner. +… more
- Cordis (Irvine, CA)
- …treatments for coronary and peripheral artery diseases. With four Investigational Device Exemptions (IDEs) approved and actively enrolling patients (Coronary ISR, ... SFA, and Peripheral BTK), Cordis is leading the way in delivering transformative medical solutions. At Cordis, we're teammates, not just employees. We embrace an… 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 ... for budgeting, forecasting, long-range planning + Lead the preparation, management and presentation of the annual operating plan, long...must, Oracle Fusion a plus + Prior experience in medical device or healthcare industry a plus… more
- Edwards Lifesciences (Irvine, CA)
- …portfolio of products across TMTT. The Sr. Specialist will be an experienced medical device professional with strong scientific acumen and a commitment to ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
- ZOLL Medical Corporation (San Jose, CA)
- …At least three (3) years of field sales experience - client focus within cardiology, medical device and/or pharma industries required + Five or more years of ... cardiac death. + HFMS (https://cardiacdiagnostics.zoll.com/products/heart-failure-arrhythmia- management -system/) (Heart Failure Management system) is a non-invasive, patch-based device … more