New Product Introduction Project Manager

Intellectt INC

  • Libertyville, IL
  • 5 days ago

    Highlights

    We are seeking an experienced NPI Project Manager to lead New Product Introduction (NPI) projects within a medical device manufacturing environment. The ideal candidate will manage cross-functional teams, project timelines, product launches, and manufacturing readiness activities from development through commercialization.

    Numbers & Facts

    LocationLibertyville, IL

    Description

    Hi,
    Hope you are doing good,
    My name is Ayaan, and I'm a Senior Recruiter at Intellectt Inc. I came across your profile and believe your experience could be a good match for an exciting opportunity I'm currently working on.
    If you're interested, please send your updated resume to ayaan.f@intellectt.com
    Title: Product Introduction Project Manager
    Location: Libertyville, IL
    Durations: Long-Term
    Position Summary
    We are seeking an experienced NPI Project Manager to lead New Product Introduction (NPI) projects within a medical device manufacturing environment. The ideal candidate will manage cross-functional teams, project timelines, product launches, and manufacturing readiness activities from development through commercialization.
    Key Responsibilities
    Lead and manage NPI projects for medical device products.
    Coordinate cross-functional teams including Engineering, Quality, Manufacturing, Supply Chain, and Regulatory.
    Drive project timelines, budgets, risk management, and deliverables.
    Support product transfer, process development, and manufacturing scale-up activities.
    Ensure compliance with FDA, GMP, and quality system requirements.
    Track project progress and communicate updates to stakeholders and leadership.
    Required Qualifications
    Bachelor's degree in Engineering, Life Sciences, or related field.
    10+ years of project management experience in medical device manufacturing.
    Strong knowledge of NPI, product lifecycle management, and manufacturing operations.
    Experience working in regulated FDA/GMP environments.
    Excellent leadership, communication, and organizational skills.

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