- VTI Life Sciences (San Diego, CA)
- …engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support ... Manufacturing Systems and Vision Sensors. Experience in manufacturing and testing of Medical Devices . + Proficiency in Microsoft Office including Word, Excel,… more
- Dignity Health (Sacramento, CA)
- **Responsibilities** + Ensures a high quality medical staff by thoroughly investigating and verifying the credentials of all applicants to the medical staff ... staff/Allied Health categories + Provides a vehicle to improve quality via the medical staff committee process...monitoring and planning for budgets and expenses + Promotes medical staff compliance with regulatory and accreditation… more
- Actalent (San Diego, CA)
- …receipt, and implementation of new and revised labeling. Required Skills: + Experience in medical device labeling and regulatory compliance + Proficiency in ... labeling process for both new and existing in vitro diagnostic (IVD) and medical device (MD) products. This role requires cross-functional collaboration to… more
- Terumo Neuro (Aliso Viejo, CA)
- …Staff Optical Engineer, R&D **Job Description:** Support the design and manufacture of medical devices , including creating 3-D designs using a design software ... post market phases. Work closely with R&D counterparts, Operations, Quality , and Regulatory in supporting the development...Minimum six (6) years of relevant work experience in medical device industry. 3. Strong written and… more
- Stryker (Irvine, CA)
- …design, develop, modify, and verify mechanical components for medical devices while working cooperatively with R&D, Quality , Manufacturing, Regulatory ... venous and other vascular diseases through purpose-driven innovation. As a fast-growing medical device company, we develop breakthrough technologies that treat… more
- Fresenius Medical Center (Riverside, CA)
- …for patient medical records and state regulations. + Provides outstanding quality of patient care by supporting and driving FMCNA quality standards ... regulatory requirements and the practice of Continuous Quality Improvement (CQI), including use of FMCNA CQI tools....facility specific action plans in order to achieve FMCNA quality standards. + Ensures medical records are… more
- Terumo Neuro (Aliso Viejo, CA)
- …and experience. 2. Minimum five (5) years of relevant experience in product labeling in medical device field. 3. Minimum one (1) year of experience in project ... 12. Minimum seven (7) years of relevant experience in product labeling in medical device field. **External-Facing Title:** Sr Labeling Lead **Posting Country:**… more
- Edwards Lifesciences (Irvine, CA)
- …statistics, regulatory and payer landscapes, and evidence requirements for medical devices . + Experience engaging with external stakeholders to support ... managing multiple RWE projects concurrently-both internally and with consultants-within the medical device , pharmaceutical, or healthcare industry. + Proficiency… more
- J&J Family of Companies (Irvine, CA)
- …Product Security strategy and framework throughout Johnson & Johnson Vision (JJV) medical device portfolio. This includes identifying key strategy and goals, ... and enforce Product Security governance model for JJV pre and post market medical devices . + Perform automated code scanning and coordinate formal security… more
- Abbott (Santa Clara, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... you dream of. + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO...Our business purpose is to restore health and improve quality of life by designing and providing device… more