- Abbott (Alameda, CA)
- …of clinical studies from concept to clinical study report per timelines and quality standards. **This role is located in Alameda, California.** **What you'll do:** + ... + Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines,… more
- Fujifilm (Sacramento, CA)
- …of the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all ... level of success with yearly goals provided by your manager and metrics defined on a team level. +...with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard… more
- Fujifilm (Sacramento, CA)
- …opinion leaders in the Endoscopy space. The role of the Business Development Manager is to understand and define our internal and external endoscopic customers' ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Danaher Corporation (Lodi, CA)
- …and chart the course for continuous improvement of OEE and maintenance processes for compliance with Company, FDA , ISO, OSHA and GMP regulations. The essential ... processes in our IVD Factory. This position reports to the Maintenance Engineering Manager and is part of the Engineering team located in Lodi, California and… more