Project Manager

Stereotaxis Inc

  • Minneapolis, MN
  • 30+ days ago
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    Skills

    • Alliance/Partner Managementunmatched
    • Budget Managementunmatched
    • Cardiovascular Diseaseunmatched
    • FDA (Food and Drug Administration)unmatched
    • ISO (International Organization for Standardization)unmatched
    • Industry Standardsunmatched
    • Maintain Complianceunmatched
    • Medical Equipmentunmatched
    • Patient Careunmatched
    • Problem Solving Skillsunmatched
    • Product Developmentunmatched
    • Product Managementunmatched
    • Product Supportunmatched
    • Project Planningunmatched
    • Project/Program Managementunmatched
    • Regulationsunmatched
    • Regulatory Complianceunmatched
    • Requirements Managementunmatched
    • Risk Analysisunmatched
    • Risk Managementunmatched
    • Strategic Planningunmatched
    • Technical Leadershipunmatched
    • Technical Supportunmatched
    • Time Managementunmatched
    • Traceabilityunmatched

    Description

    Company Description:

    Stereotaxis is the global leader in innovative robotic technologies designed to enhance the treatment of arrhythmias and perform endovascular procedures. Its mission is the discovery, development and delivery of robotic systems, instruments, and information solutions for the interventional laboratory. These innovations help physicians provide unsurpassed patient care with robotic precision and safety, improved lab efficiency and productivity, and enhanced integration of procedural information. Core components of Stereotaxis' systems have received regulatory clearance in the United States, European Union, China, Japan, Canada, and elsewhere. For more information, please visit www.stereotaxis.com.

    Position Summary:

    The Project Manager will be responsible for overseeing and managing the development of new products from concept to market launch while ensuring that projects are completed on time, within scope, and on budget, while maintaining strict compliance with industry standards.

    Essential Responsibilities:

    • Develop and maintain detailed project plans, including timelines, milestones, and deliverables.
    • Manage product requirements and traceability.
    • Lead design review and risk management activities.
    • Manage technical partners/ vendors supporting product development activities.
    • Ensure all projects comply with FDA, ISO 13485, and other relevant medical device industry regulations and standards.
    • Identify potential project risks and develop mitigation strategies. Conduct regular risk assessments and adjust plans as needed to address emerging issues.
    • Other assignments as requested.

    Numbers & Facts

    LocationMinneapolis, MN

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