- Astellas Pharma (South San Francisco, CA)
- …projects from concept to delivery. + Experience working cross-functionally with compliance, regulatory , sales, and medical affairs teams. + Excellent ... The DIGITIVA solution is a combination of a hardware medical device , a patient-facing mobile app, and...(MAP) team to ensure all marketing materials meet compliance, regulatory , and legal requirements. + Maintain thorough documentation and… more
- J&J Family of Companies (Santa Clara, CA)
- …appropriate methods and techniques for evaluations. + Collaborate with R&D, Marketing, Medical Safety, Regulatory Affairs , Clinical Engineering, and Quality ... human factors engineering. + Solid understanding of ISO 14971 and IEC 62304. + Medical Device product development or experience working in a highly regulated… more
- Edwards Lifesciences (Irvine, CA)
- …assigned studies + Contributing to additional initiatives that shape the future of medical device development **What you'll need (Required):** + Ph.D. or ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you… more
- Envista Holdings Corporation (Brea, CA)
- …+ Minimum of 5 years of experience in technical writing, preferably within the medical device or healthcare industry. Experience in orthodontics is a significant ... professionals worldwide. + Collaboration: Work closely with product marketing, clinical affairs , research and development, sales, and regulatory teams to… more
- Fujifilm (Sacramento, CA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... expense tracking and reporting (Salesforce.com) + Where appropriate, collaborate with the Medical Affairs Team. + Follow up to define pathway and respond to… more
- J&J Family of Companies (Irvine, CA)
- …execution including timelines milestones and budgets + Lead efforts co-ordinating with Medical Affairs organization to facilitate data coding and safety reviews ... with at least 6 years of clinical data management experience in Medical Device or Pharmaceuticals including experience of successful active participation… more
- J&J Family of Companies (Santa Clara, CA)
- …operate and handle various laboratory equipment is desired + Experience working in medical device is advantageous + Familiarity with GLP requirements is required ... Clara, CA.** **Purpose:** The Preclinical Laboratory Operations Administrator in Preclinical Affairs will work within the animal facilities of Johnson & Johnson… more
- Danaher Corporation (Sunnyvale, CA)
- …marketplace highly desired. + Demonstrated experience in Product Management in the Medical Device and Diagnostics industry highly desired Cepheid, a Danaher ... core team stakeholders such as Project Management, Portfolio Management, R&D, Quality, Regulatory , and Clinical Affairs . The essential requirements of the job… more
- Insight Global (Irvine, CA)
- …company located in Irvine, CA. This person will be responsible for working with regulatory affairs , Research & Development, Supply Chain, and Quality to support ... projects concerning one medical device unit, planning integration, etc. Specifically this candidate will assist in supply network planning/inventory planning… more