- Actalent (Irvine, CA)
- …manufacturing engineering, and process improvement. + Familiarity with ISO 9001 standards and medical device regulations. + Ability to perform root cause and ... in a fast-paced environment. + Experience in contract manufacturing and working with medical device equipment. Work Environment The position is based in a… more
- Fujifilm (Sacramento, CA)
- …manager, senior product manager, product/technical director). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience ... global R&D, operations, regulatory, global marketing, infection control, other companies/ device manufacturers, etc.) + Build and maintain strong relationships with… more
- GRAIL (Menlo Park, CA)
- …related disciplines is strongly desired. + Experience working on IDE trials and device registries within the medical device and/or pharmaceutical industry. ... visit grail.com . The Senior Clinical Data Manager (CDM) will lead data management activities for one or multiple diagnostic product development studies in support… more
- Cordis (Irvine, CA)
- …supervisory experience, or equivalent work experience + 5+ years' experience in the medical device /pharmaceutical field or in a related area. + Excellent written ... the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery… more
- CalSTRS (Sacramento, CA)
- …The ideal candidate will possess the following skills: + Extensive supervision and management experience with the ability to effectively manage a team of accounting ... of pension laws, rules and regulations. + Strong project management experience or proven ability to lead, monitor and...+ Flexible work hours + Remote work options + Medical benefits, including health, dental and vision insurance +… more
- Philips (San Diego, CA)
- …solutions through product development, integration and V&V, ensuring compliance with medical device standards and global regulatory requirements. + You ... and thorough manner. + You have experience working in the regulated medical device environment: demonstrating practical knowledge and experience with global… more
- Abbott (Sylmar, CA)
- …such as Azure Databricks. + Experienced in the sequential phases of the medical device development from early feasibility and VOC through development, test, ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- WM (Salinas, CA)
- …Since our founding over 30 years ago, we have grown from a small start-up in medical waste management into a leader across a range of increasingly complex and ... and well-being in a safe, responsible, and sustainable way. **Position Purpose:** The Medical Waste Route Driver CDL A is responsible for servicing assigned accounts… 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
- Abbott (Pleasanton, CA)
- …to define and implement comprehensive test automation strategies for Abbott's next-generation medical device software portfolio (Class II and Class III devices). ... & Quality Assurance: Ensure all test strategies and practices align with medical device regulatory standards (FDA, ISO, IEC 62304).Support documentation,… more