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    Quality Specialist - London, United Kingdom - Tec Partners

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    Description

    TEC Partners is pleased to have partnered with a pioneering medical device company dedicated to improving the quality of life for patients through next-generation orthopedic implant devices.

    Through events, resources, and patient information, my client aims to empower both medical professionals and patients on their journey to improved orthopedic health.

    Quality Specialist

    As the Quality Specialist, you will play a pivotal part in upholding the company's commitment to quality and compliance with ISO 13485 standards.

    As a key member of the quality assurance team, you will be responsible for conducting internal audits, leading lean manufacturing initiatives, driving supply chain improvements, and conducting supplier audits to ensure the highest standards of product excellence.


    Quality Specialist Responsibilities:
    Conduct internal audits to ensure adherence to quality management systems and regulatory requirements
    Drive continuous improvement initiatives throughout the supply chain to enhance product quality and reliability
    Conduct supplier audits to evaluate performance and ensure compliance with quality standards and regulatory requirements
    Develop and maintain documentation related to quality management systems and regulatory compliance
    Provide guidance and support to team members on quality assurance processes and best practices


    Quality Specialist Requirements:
    Bachelor's degree in a Scientific related field or equivalent experience in a commercial manufacturing organisation
    Minimum of 3 years of experience in quality assurance within the medical device industry
    Strong knowledge of ISO 13485 standards and regulatory requirements
    If you are passionate about quality assurance and committed to driving excellence in orthopedic implant devices, please apply with an up to date CV #J-18808-Ljbffr

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