- 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
- 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
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …+ Demonstrated expertise in applying FDA design control requirements (21 CFR ) as applied to medical device software and medical device regulation ... **Job Description** We're looking for a Principal Software Engineer to join our...with states and local laws. **Company benefits** : Comprehensive medical , dental, vision, prescription drug coverage, company provided basic… more
- Medtronic (Fridley, MN)
- …organization in the definition, design, development, and testing of complex medical device systems within the Neuromodulation Operating Unit. Neuromodulation ... **Careers That Change Lives** In this role as a ** Principal Systems Engineer** , you will have responsibility for...system verification and validation strategy and testing. + Previous medical device experience with a history of… more
- Medtronic (Minneapolis, MN)
- …following and other duties may be assigned. + Develop, characterize, and validate medical device manufacturing processes. + Provide guidance and knowledge on ... in the Life** In this exciting role as a Principal Quality Engineer, you will have responsibility for manufacturing...experience in Engineering and/or Quality **Nice to Have** + Medical device , pharma, or drug- device … 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)
- …to innovation in a more connected, compassionate world. **A Day in the Life** Principal Materials Engineer Careers That Change Lives At Medtronic, we push the limits ... materials selection, processing, analysis, biostability, and process-property-performance relationships for medical devices. Additionally, the individual will serve as a… more
- Abbott (St. Paul, MN)
- …of FDA, IEC 60601, GMP, ISO 13485, and ISO 14971 + Prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn more about our ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Medtronic (Fridley, MN)
- …Cognitive Psychology, HCI, or closely related field is preferred + Experience with medical device standards, regulations, and compliance + Comfortable working in ... drive healthcare forward and remain a global leader in medical technology and solutions. **Careers That Change Lives** In...That Change Lives** In this impactful role as a Principal Human Factor Design Engineer, you will play a… more