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    Associate Manager QA - Medical Device Plant Compliance

    FukushimaPermanent¥11M to ¥14M
    Back to job search
    4 days ago
    JN -012026-1995448

    Associate Manager QA - Medical Device Plant Compliance

    Fukushima Permanent ¥11M to ¥14M English: Intermediate/Business Japanese: Native

    Associate Manager QA - Medical Device Plant Compliance

    About the job

    A global medical technology company is seeking an Associate Manager, Quality Assurance to lead production quality and compliance at its medical device manufacturing site in Fukushima. This is a key leadership role focused on ensuring product safety, manufacturing excellence, and compliance with global quality standards and Japanese medical device regulations. You will manage and develop a QA team while partnering with global stakeholders to maintain world-class quality systems for life-saving medical devices.

    Key Responsibilities

    • Review and approve production documentation to ensure products meet safety and regulatory requirements
    • Identify and resolve quality issues related to materials or finished products that fall outside standards
    • Lead investigations into customer complaints to identify root causes and implement corrective actions
    • Manage technical and manufacturing changes to ensure product quality and compliance are maintained
    • Oversee product testing activities and collaborate with global teams to ensure alignment with international regulations

    Required Skills and Qualifications

    Experience:
    • 5+ years of experience in a technical role such as quality assurance, quality control, or manufacturing
    • 3+ years of experience leading and managing a team
    • Strong understanding of international quality standards and Japanese medical device laws
    • Ability to relocate to or live near Fukushima
    Soft Skills:
    • Strong analytical mindset with the ability to solve complex quality issues using data and logical thinking
    • Coaching-oriented leadership style that supports team development and growth
    • Strong collaboration skills for working across cultures in a fast-paced environment
    Language Requirements:
    • Japanese: Native-level proficiency
    • English: Intermediate to Business-level proficiency (professional speaking and writing required)

    Preferred Skills & Qualifications

    • Experience with Lean, Six Sigma, or continuous improvement methodologies
    • Green Belt certification is a plus
    • Experience leading end-to-end projects from planning through execution

    About the Company

    Our client is a global medical technology company dedicated to improving patient outcomes through advances in medical discovery, diagnostics, and healthcare delivery. They manufacture a wide range of medical devices, laboratory equipment, and healthcare supplies used by institutions and researchers worldwide.

    Why You'll Love Working Here

    • Lead quality and compliance for life-saving medical devices with real impact on patient safety
    • People management role with opportunities to coach and develop a dedicated QA team
    • Work in a global environment with exposure to international quality systems and stakeholders
    • Strong career progression in a highly regulated and high-value manufacturing setting
    • Opportunity to take ownership of quality improvement and compliance leadership at plant level

    Don't Miss Out - Apply Now!

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