- Abbott (Menlo Park, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... Our business purpose is to restore health and improve quality of life by designing and providing device...Qualifications** + Professional certification(s) desirable + Experience in the medical device industry + Bachelor's Degree in… more
- Globus Medical, Inc. (Redwood City, CA)
- …3 years with a PhD - related experience with development or verification in the medical device industry. (class III medical device experience preferred). ... At Globus Medical , we move with a sense of urgency...and reports, and validation plans and reports. Works with Quality and Regulatory Engineers for the release… more
- Abbott (San Diego, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... + Minimum 15 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD… more
- Philips (San Diego, CA)
- …You have a minimum of 8+ years' experience in FDA regulated, IEC 62304 medical device software environments (SiMD/SaMD), with a focus on Software Design ... practices, cutting-edge tools, and innovative methodologies to continuously enhance software quality and regulatory compliance. + Will oversee the development,… more
- Medtronic (Northridge, CA)
- …Technical degree is a plus. + Experience with Design Control documentation within medical device industry or Pharma industry. + Experience conducting and ... This role is critical to ensuring that products meet regulatory requirements and quality standards throughout the...self-motivation. + Prior work experience in a regulated industry ( Medical Device Industry preferred) + Sound experience… more
- Abbott (San Diego, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... frameworks) + Knowledge of design controls and regulations for medical device development is a plus +...device development is a plus + Understanding of quality software engineering principles aligned with ISO, IEEE, or… more
- Terumo Neuro (Aliso Viejo, CA)
- …3. Strong knowledge of medical device development processes, regulatory requirements, and quality management systems. 4. Excellent analytical skills to ... enhancements. + Stay current with industry trends, regulations, and best practices in medical device project management, and apply them to improve project… more
- NTT America, Inc. (Sacramento, CA)
- …of data center knowledge and is responsible for the operational integrity and regulatory compliance of the data center electrical, mechanical, and fire life safety ... data center problems are identified and repaired quickly, that contractors deliver quality services, and that internal customer demands are met. **ESSENTIAL DUTIES &… more
- AbbVie (South San Francisco, CA)
- …science or a related field with relevant experience in pharma, academia, healthcare and/or medical device industries; MBA or consulting experience a plus. + MS ... Purpose AbbVie's Digital Science Team is an innovative group that combines medical knowledge, digital technologies, regulatory , and data science expertise to… more
- Bausch + Lomb (Sacramento, CA)
- …Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and Clinical ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… more