- Medtronic (Mounds View, MN)
- …both your technical breadth and business acumen to support the newly approved therapy medical device software and participate in the design and development ... more connected, compassionate world. **A Day in the Life** Principal Software Engineer - Product Security Careers...Ensure compliance with industry standards and regulations related to medical device and health software … more
- Philips (Plymouth, MN)
- …medical device industry. This includes demonstrated success in bringing software -intensive medical devices to market and leading teams in multiple product ... ** Principal Software Architect- Clinical Imaging ...in clinical applications, systems integration, interoperability, and knowledge of medical device regulations like IEC 62304, FDA,… more
- Medtronic (Minneapolis, MN)
- …healthier lives. The Principal Compliance Audit Specialist focus will be primarily medical device software , product security, and risk management. We ... requirements for Software and Product Security to identify gaps in medical device software . + Provide detailed functional knowledge and maintain insight… more
- Medtronic (Mounds View, MN)
- …innovation in a more connected, compassionate world. **A Day in the Life** Senior Principal Software Product Owner Careers That Change Lives Together, we can ... Cardiac Rhythm Management group is looking for a Senior Principal Software Product Owner to join our...+ Familiarity with the technology stacks related to FHIR, Medical Device data, 3rd party integrations, Data… more
- Abbott (Plymouth, MN)
- …necessary detail. + Maintains ongoing surveillance and analysis of all pertinent medical device regulations to ensure submission requirements worldwide are ... supplements and US device regulations, or with EU and other international medical device regulations and submissions. + Must be familiar with relevant… more
- Medtronic (Minneapolis, MN)
- …profile._ + Bachelor's degree in a technical discipline + Minimum 7 Years of medical device regulatory experience with Bachelor's degree + Or minimum 5 Years ... people with cardiac arrhythmias and heart failure. Preference for software -based regulatory experience or familiarity with software ...of medical device regulatory experience with an advanced… more
- Medtronic (Fridley, MN)
- …+ Maintain up-to-date knowledge of cybersecurity regulations and standards specific to the medical device industry (FDA, HIPAA, IEC 62443, NIST, NIS 2, etc.). ... GRC (Governance, Risk, & Compliance), or external/internal audit, preferably within the medical device or healthcare industry. + Strong understanding of… more
- Philips (Plymouth, MN)
- …of 8+ years' Regulatory Affairs experience within FDA regulated Medical Device /HealthTech product environments. Experience with Software as Medical ... critical member of the Philips Ultrasound- Regulatory Affairs Organization, the Principal Regulatory Affairs Specialist will lead and provide regulatory oversight… more
- Fairview Health Services (Minneapolis, MN)
- **Job Overview** Job Summary: Principal Cybersecurity Analyst, is responsible to provide technical leadership, collaboration and drive to help elevate Cybersecurity ... of security including authentication, authorization, network security, data, system device and Operating Systems, coding principles, development methodologies, web/mobile… more
- Medtronic (Mounds View, MN)
- …years of experience in marketing, quality, and/or field support roles within the medical device , healthcare, or life sciences industryto leverage in discussions ... compassionate world. **A Day in the Life** The Sr. Principal Marketing Quality Program Manager serves as the critical...planning for revisions and follow-ups to initial actions (ie, software updates) + CRM CAPA triage boardunderstand and providing… more
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