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    EN日本

    Quality Assurance Specialist - Medical Device Compliance

    TokyoPermanent¥5.5M to ¥8M
    Back to job search
    1 week ago
    JN -012026-1994385

    Quality Assurance Specialist - Medical Device Compliance

    Tokyo Permanent ¥5.5M to ¥8M English: Intermediate/Business Japanese: Native

    Quality Assurance Specialist - Medical Device Compliance

    日本語で読む

    About the job

    An established global medical device manufacturer is seeking a Quality Assurance Specialist to strengthen its complaint handling and quality assurance operations in Japan. This role plays a critical part in ensuring patient safety, regulatory compliance, and product quality, working closely with global manufacturing sites and international stakeholders. You will act as a key liaison between Japan and global headquarters while contributing to continuous quality improvement initiatives.

    Key Responsibilities

    • Investigate medical device product complaints and collaborate with global manufacturing sites to verify technical findings
    • Identify root causes of quality issues and work with overseas teams to implement preventive actions
    • Provide expert quality and technical guidance to customers, internal engineers, and cross-functional teams
    • Analyze market and complaint data to identify trends and recommend product or process improvements
    • Serve as the main point of contact between global headquarters and local teams to ensure clear and effective communication

    Required Skills and Qualifications

    Experience:
    • Minimum 3+ years of experience in quality assurance, with hands-on involvement in product complaint handling
    • Experience in medical devices or another highly regulated industry is strongly preferred
    • Solid understanding of quality systems and structured problem-solving methodologies
    Soft Skills:
    • Ability to clearly explain technical information to multicultural and cross-functional stakeholders
    • Strong analytical mindset with a logical approach to identifying and resolving quality issues
    • Collaborative working style with the ability to partner effectively with engineering, sales, and global teams
    Language Requirements:
    • Japanese: Native level
    • English: Intermediate to Business level (used for global meetings and technical documentation)

    Preferred Skills & Qualifications

    • Practical experience with medical device regulations and quality management systems
    • Strong working knowledge of ISO 13485 standards

    About the Company

    Our client is a global manufacturer of professional dental products and technologies, supplying advanced tools and solutions used by dentists worldwide. Their portfolio includes X-ray systems, dental instruments, and prosthetic solutions. With a strong international footprint, the company is committed to innovation, quality, and improving patient outcomes across global markets.

    Why You'll Love Working Here

    • Build a global career by collaborating daily with international teams across Europe and the Americas
    • Play a meaningful role in improving patient safety through high-quality medical device standards
    • Enjoy excellent work-life balance with flexible working hours and remote work options
    • Join a stable, well-established organization with long-term career growth opportunities

    Don't Miss Out - Apply Now!

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