- Abbott (Alameda, CA)
- …medical devices, customer complaints, and product nonconformances. Prior experience in the medical device industry and/ or quality systems are required. + ... working knowledge of FDA Code of Federal Regulations as it applies to medical device manufacturing, including cGMP, ISO14971, as well as complaint handling… more
- Abbott (Alameda, CA)
- …they apply to the development, verification, validation, use, and maintenance of medical device software. + Coordinate activities with other engineering ... to the development, verification, validation, and maintenance of application in support of medical device software. + Software Quality lead in various phases of… more
- Stanford University (Stanford, CA)
- …including: Epilepsy, Neuorimmunology/Multiple Sclerosis, Alzheimers, Autonomic Disorders, Device Neurosurgery, Stem Cell Neurosurgery, Headache, Radiology, ... of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and… more
- Cedars-Sinai (Los Angeles, CA)
- …will be involved in the development and possible commercialization of a novel medical device technology. Interest or experience in a start-up environment with ... will assist in the effort in validating the clinical trial of groundbreaking medical imaging systems. The job will provide an outstanding opportunity to work with… more
- Terumo Neuro (Aliso Viejo, CA)
- …of ten (10) years of relevant manufacturing process development experience in the medical device industry. 3. Strong written and verbal communication skills. 4. ... of twelve (12) years of relevant manufacturing process development experience in the medical device industry. 3. Ability to design, develop, and validate… more
- Stryker (Irvine, CA)
- …venous and other vascular diseases through purpose-driven innovation. As a fast-growing medical device company, we develop breakthrough technologies that treat ... Staff R&D Engineer supports and leads project teams in the development of medical device products - this includes writing or verifying specifications, developing… more
- Abbott (Sylmar, CA)
- …environment in quality desired. + Industry certification preferred. + Class III or II medical device experience. + 3-5 years in a supervisory/leadership role. + ... such as Quality, Compliance, Engineering, within a regulated environment, such as medical device , diagnostics or pharmaceutical industries, to develop the… more
- Abbott (Pleasanton, CA)
- …Qualifications** + Master's Degree. + Minimum 5 years working with in a medical device manufacturing company or similarly regulated industry. Apply Now ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Abbott (Temecula, CA)
- …writing skills. **Preferred Qualifications** + Masters Degree Preferred + Prior medical device experience preferred. ASQ CQE certification preferred. Design ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… 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 ... Awareness: Stay current with industry developments, market changes, and regulatory modifications that may affect the business. These responsibilities...not be debarred by FDA for work in any Medical Device business. + Must have a… more