- Fujifilm (St. Paul, MN)
- …and II + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...Provides on-going support to resolve application related and image quality concerns on both a product and system level.… more
- Philips (Plymouth, MN)
- …the right fit if:** + You have a minimum of 8+ years' experience in FDA regulated, IEC 62304 medical device software environments (SiMD/SaMD), with a ... performance management, technical/professional development and mentorship to engineers and quality teams, helping them meet schedules, resolve technical challenges,… more
- Abbott (St. Paul, MN)
- …use of quality tools/methodologies + Advanced Degree + Prior medical device experience + Experience working in a broader enterprise/cross-division ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Abbott (Plymouth, MN)
- …automation, and process control. **Preferred Qualifications** + Experience in the ** medical device industry** , particularly with **catheter manufacturing** or ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Fujifilm (St. Paul, MN)
- …management. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... and or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a… more
- Abbott (St. Paul, MN)
- …and market success. + **Technical & Regulatory Acumen** : Deep understanding of medical device standards and regulatory frameworks (eg, IEC 60601, IEC 62304, ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- TE Connectivity (Plymouth, MN)
- … Quality Engineering, Purchasing, and Sales Engineering, to launch medical products. + Properly document and internally communicate all technical discoveries, ... to meet customer requirements within scope (eg, performance and quality ), schedule (eg, on time delivery), and budget (eg,...and development engineering experience with a BS degree + Medical product development experience and knowledge of FDA… more
- Medtronic (Mounds View, MN)
- …years of relevant experience **Preferred Qualifications** + Knowledge of Medical device software development, IEC-62304 and FDA guidance in a technical ... a critical part in enhancing and streamlining our software development, testing, and quality assurance processes. You will develop a variety of tools, scripts, and… more
- Fujifilm (St. Paul, MN)
- …or processes. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... must have expert level knowledge in all areas of medical informatics, IT infrastructure design and deployment, medical...with MI Project Management (PM) team to deliver high quality Synapse product solutions. + Act as primary technical… more
- Fujifilm (St. Paul, MN)
- …as assigned. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more