- Abbott (Sylmar, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... staff in the company. + Gathers and analyzes input requirements for medical devices , supporting instrumentation/service infrastructure, and translates these into… more
- Abbott (Alameda, CA)
- …relate to the development, verification, validation, and maintenance of application in support of medical device software. + Software Quality lead in various ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Danaher Corporation (Brea, CA)
- …would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Certifications such as CQE, CQA, Six Sigma, ... qualifications, and ongoing performance assessments to ensure adherence to internal quality standards, customer requirements, and applicable external regulatory … more
- Envista Holdings Corporation (Pomona, CA)
- …related field; Master's degree preferred + 5+ years of experience in Engineering; medical device or similar regulated industry highly preferred + Strong ... working closely with cross-functional teams to develop, implement, and maintain quality assurance protocols that comply with regulatory requirements and… more
- Abbott (San Diego, CA)
- … devices and supporting software. + Collaborate with engineering, quality , and regulatory teams to apply secure-by-design principles throughout development. ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....field. + 6+ years of experience in embedded systems, medical device development, or product cybersecurity. +… more
- BD (Becton, Dickinson and Company) (Milpitas, CA)
- …planning for marketing collateral to support clinical products + Ownership of on-time quality assessments, medical device reporting and health risk ... bodies + Provide subject matter expertise into design of clinical trials for medical device development and submission to the FDA and other regulatory… more
- BD (Becton, Dickinson and Company) (Irvine, CA)
- …development from concept to market + Strong knowledge of regulatory requirements and quality standards in the medical device industry (FDA, ISO 13485, ... and translate detailed information about user interactions with Critical Care medical devices and connectivity solutions through various methods (interviews,… more
- Hologic (San Diego, CA)
- …practices, particularly in Breast/GYN or General Surgery. + Strong knowledge of medical device regulations, compliance standards, and risk management processes. ... Safety Officer San Diego, CA, United States Hologic's Quality team is seeking a Medical Safety...Awareness of digital medicine and artificial intelligence integration in medical devices . **Skills** + Advanced ability to… more
- Danaher Corporation (Sunnyvale, CA)
- …Union In Vitro Diagnostic Regulation (IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) ... Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Quality Systems Specialist is responsible for functioning as Lead… 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 ... relevant engineering/technical degree and 10 years' experience in the medical device industry or a Master's Degree...or a Master's Degree and 8 years' experience in medical devices . + 3+ years of experience… more