- Abbott (Plymouth, MN)
- …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Senior Facilities Program Manager ** **Working at Abbott** At Abbott, ... (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program , and FreeU… more
- Medtronic (Fridley, MN)
- …driving the successful delivery of engineering projects and the SPC deployment program . At Medtronic, we bring bold ideas forward with speed and decisiveness ... to engineer the extraordinary. + Lead Global SPC Deployments Program over multiple sites + Develop and manage ...the project lifecycle + Medical device / regulated / FDA environment + Developed and implemented culture change +… more
- Abbott (St. Paul, MN)
- …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Senior Operations Manager ** **Working at Abbott** At Abbott, you can do ... providing device and management solutions for treating structural heart disease. The ** Senior Operations Manager ** is responsible for managing, supervising, and… more
- Medtronic (Mounds View, MN)
- …in a more connected, compassionate world. **A Day in the Life** The Senior Quality Systems Manager drives the evolution of Medtronic's product development ... with medical device standards. + Maintain deep familiarity with FDA 21 CFR Part 820, ISO 13485, and other...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
- Fujifilm (St. Paul, MN)
- **Position Overview** The Senior Project Manager , SDS manages, leads, and coordinates all aspects of the Synapse MI implementation process from quotation to ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Medtronic (Minneapolis, MN)
- …in a more connected, compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist is responsible for planning and executing global regulatory ... potential regulatory issues and questions from regulatory agencies. + Prepare FDA submissions and European Technical Files/Technical Documentation (MDD and MDR) for… more
- Medtronic (Fridley, MN)
- …in a more connected, compassionate world. **A Day in the Life** The Senior Import Analyst performs analysis and executes project and transactional needs within the ... with regulatory requirements for US and Canada imports (eg, Customs, FDA , Health Canada, and Participating Government Agencies). Collaborates with 3rd party… more
- Celestica (Maple Grove, MN)
- …customers, suppliers, and partners, and ensuring compliance with regulatory requirements ( FDA , ISO, ASQ, RAC). The position is virtual, offering competitive ... compensation and career growth opportunities. Significant experience with FDA certification processes is required. **Candidate Profile** The Director, Global Quality… more
- Medtronic (Mounds View, MN)
- …innovation in a more connected, compassionate world. **A Day in the Life** The Senior Product Security Engineer plays a critical role in ensuring the security of ... and extend life."_ **A Day in The Life** The Senior Product Security Engineer plays a critical role in...strategies in accordance with IEC 81001-5-1, ISO 14971, and FDA premarket cybersecurity guidance. + **Security Architecture & Design**… more
- Medtronic (Fridley, MN)
- …opening will close on - 5 October 2025. We are seeking a Senior Software Automation Engineer to lead software and controls integration for automated manufacturing ... systems meet both technical specifications and regulatory standards (eg, FDA , 21 CFR Part 11). You'll work closely with...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
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