Project Manager - Medical Device

MRINetwork Jobs

  • 30+ days ago
  • Remote
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    Skills

    • Atlassian JIRAunmatched
    • Cross-Functionalunmatched
    • Document Change Managementunmatched
    • Document Managementunmatched
    • Documentationunmatched
    • Electromechanicsunmatched
    • FDA (Food and Drug Administration)unmatched
    • Follow Throughunmatched
    • Hardware Administrationunmatched
    • Hardware Developmentunmatched
    • Hardware-Software Integrationunmatched
    • Healthcare Qualityunmatched
    • ISO (International Organization for Standardization)unmatched
    • Lean Six Sigmaunmatched
    • Medical Equipmentunmatched
    • Organizational Skillsunmatched
    • Project Designunmatched
    • Project Engineeringunmatched
    • Project Management Professional (PMP)unmatched
    • Project Planningunmatched
    • Project Scheduleunmatched
    • Project Trackingunmatched
    • Project/Program Managementunmatched
    • Regulationsunmatched
    • Scalable System Developmentunmatched
    • Software Administrationunmatched
    • Software Developmentunmatched
    • Startupunmatched
    • Time Managementunmatched

    Description

    Project Manager (Medical Device / FDA Environment)

    Location: Remote (Periodic onsite in Columbus, OH – ~1x/month initially)

    Engagement: Part-Time (~20–25 hours/week) - TBD based on intended milestones and needs

     


    Overview

    We are seeking a hands-on Project Manager to help drive execution across a fast-moving, early-stage medical device environment. This role will bring structure, visibility, and accountability to cross-functional initiatives, ensuring projects stay on track while aligning with FDA and quality system expectations.

     

    This is a remote part-time/fractional role with nominal 20-25 hours per week anticipated.  

     


    Key Responsibilities

    Establish and maintain a single integrated project schedule across engineering, clinical, quality, and regulatory teams, serving as the “schedule of truth” that aligns priorities, milestones, and dependencies.

     

    Lead recurring milestone and status meetings, ensuring risks, timelines, and cross-functional dependencies are clearly understood, while driving follow-through, documentation readiness, and timely decision-making across the organization.

     

    Coordinate execution across teams, integrating inputs from hardware and software development efforts, including interfacing with Jira to understand software progress, track issues, and reflect updates in overall project plans.

     

    Support execution within an FDA-regulated environment by aligning project activities with design controls, DHF documentation, and change management processes within the QMS.

     

    Introduce and apply structured project management methodologies (PMP, Lean, Six Sigma, or similar) to improve visibility, reduce schedule slippage, and build scalable operating rhythms appropriate for a startup environment.

     


    Preferred Experience

    Experience managing projects in medical device or FDA-regulated environments, with familiarity in design controls, DHF processes, and ISO 13485. Background supporting both software and hardware development efforts is preferred, particularly in electromechanical or software-containing products. Experience working in early-stage or evolving environments is highly valued.

     


    Profile

    An organized, proactive project manager who can bring structure without over engineering process, operate effectively in ambiguity, and keep cross-functional teams aligned and moving forward in a regulated environment.

     


    Engagement

    Approximately 20–25 hours per week, primarily remote, with occasional onsite presence (1/month) early on to build alignment and relationships with the team.

     

    Numbers & Facts

    Location (
    Remote
    )

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