- Abbott (Alameda, CA)
- …in model based design (UML or SysML), is highly desirable + Detailed experience with medical device development processes and FDA 510K and PMA regulatory ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- GRAIL (Menlo Park, CA)
- …development, clinical affairs, quality , or program management within the IVD, medical device , or pharmaceutical industries. + Regulatory affairs and IVD ... Demonstrated knowledge of US and international regulatory frameworks and processes for medical device development and approvals. + Effective collaborator in… more
- Gilead Sciences, Inc. (La Verne, CA)
- …in SAP or similar ERP systems for supplier master data + Exposure to FDA inspections, mock audits, and quality systems assessments + Strong interpersonal and ... 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 (Brea, CA)
- …need It would be a plus if you also possess : + Experience in FDA -regulated or medical device manufacturing environments. + Familiarity with ISO13485, 21 ... System (http://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Global Supplier Quality Engineer - Systems and Innovation for Beckman Coulter… more
- Danaher Corporation (Brea, CA)
- …needs It would be a plus if you also possess : + Experience in FDA -regulated or medical device manufacturing environments. + Certifications such as CQE, ... System (http://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will… more
- ManpowerGroup (Fremont, CA)
- …degree in engineering or a related field with a minimum of 7 years of medical device quality assurance experience. + In-depth knowledge of quality ... a leader in the healthcare industry, is seeking a Quality Engineer III to join their team. As a...with cross-functional teams. **What's in it for me?** + Medical , Dental, Vision, 401k with Match + Weekly pay… more
- Abbott (Alameda, CA)
- …5+ years of experience in quality assurance or regulatory compliance in the medical device industry. + Strong knowledge of ISO 13485, MDSAP, and other ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- ThermoFisher Scientific (San Francisco, CA)
- …+ 5 years of experience in a regulated industry such as pharma and/or medical device manufacturing required. Preferably within a QC GMP laboratory. + Experience ... biological products etc.), Will work with hazardous/toxic materials **Job Description** **Title: Quality Control Scientist III - Cell and Gene Therapy** As part of… more
- Neotech (Chatsworth, CA)
- Summary: Perform professional quality engineering requirements involving the application of procedural requirements and control criteria in the development and ... administration of quality procedures and techniques to assure the products meet...requirements and Board Handling. + Use of Moisture Sensitive Device (MSD) handling requirements based on component moisture sensitive… more
- VTI Life Sciences (San Diego, CA)
- …engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support ... Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training,… more