- Gilead Sciences, Inc. (La Verne, CA)
- …guard issue resolution, auto-injector issues, component manufacturing) + Understanding of Quality Management Systems and regulatory requirements + Experience ... are seeking a highly motivated **Senior Manager** to join the **Global Supplier Quality ** team within External Quality Operations. This position will support… 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) ... Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Quality Systems Specialist III is responsible for functioning as… 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 ... experience in therapeutic ultrasound research or a PhD (preferred). + Ultrasound based medical device product development is highly preferred. + May serve as… more
- Actalent (Vista, CA)
- …require. Essential Skills + ISO auditing + Quality Management System (QMS) + Quality assurance + Medical device auditing + CAPA (Corrective and ... The QA Specialist is primarily responsible for overseeing the quality and regulatory aspects of the company....etc. to FDA authorities. + File Vigilance Reports or Medical Device Reports to Competent Authority or… more
- Abbott (Sylmar, CA)
- …skills, including statistical/data analysis and report writing skills. + Prior medical device experience preferred. + Experience implementing various product ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Herbalife (Lake Forest, CA)
- …+ Knowledge of basic cGMP and QA/QC regulations for the food, pharmaceutical or medical device industry. + Familiarity with safe work practices to include proper ... Technician I, Quality Assurance - 2nd Shift Category: Quality...and SOPs + Collect samples for submission to state regulatory agency. + Sample and perform inspections of components… more
- Abbott (Pleasanton, CA)
- … quality -related issues in a timely and effective manner + Prior medical device experience preferred + Experience implementing various product and process ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Stryker (San Jose, CA)
- …required CERs, and annual updates. + Performs systematic literature reviews for medical device groups or sub-groups. Interprets literature information and ... role, you will collaborate closely with cross-functional teams, including Regulatory , Clinical, Quality , and Marketing to ensure...Knowledge and experience with MEDDEV 2.7/1 Rev. 4, EU Medical Device Regulation 2017/745 (MDR) and MDCG… more
- J&J Family of Companies (Irvine, CA)
- …years of quality , manufacturing, or research and development experience in a medical device or other regulated industry + Ability to define problems, collect ... https://www.jnj.com **Job Function:** Supply Chain Engineering **Job Sub** **Function:** Quality Engineering **Job Category:** Scientific/Technology **All Job Posting Locations:**… more
- J&J Family of Companies (Irvine, CA)
- …years of quality , manufacturing, or research and development experience in a medical device or other regulated industry + Ability to define problems, collect ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Quality Assurance **Job Category:**… more