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    Director, Quality Operations - Wilmington, United States - Global Life Science Hub

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    Description


    Global Life Science Hub is proud to announce an exciting partnership with a leading global trailblazer who is revolutionizing pharmaceutical excellence with integrated services spanning from drug development to commercialization.

    With ambitious plans to expand their Pennsylvania site by 3x fold this year, were excited to be leading a search for a brand-new Director of Site Quality Operations.


    The Director of Quality Operations will play a pivotal role in ensuring the quality, compliance and expansion of operations at the Philadelphia site.

    This position requires a dynamic leader with extensive experience in quality management, particularly in drug/device combination products, preferably with expertise in auto-injection devices.


    Position:
    Director, Quality Operations - Philadelphia


    Responsibilities:
    Lead and manage the Quality Operations teams responsible for batch record creation/review, product release, deviation management, change controls, and customer interactions
    Develop, establish, and maintain quality assurance programs, systems, and controls to ensure compliance with regulatory standards, including FDA, EMA, and other relevant agencies
    Interact with customers and regulatory agencies to ensure alignment with regulatory requirements and customer expectations
    Oversee the management of label room personnel and deviation management processes
    Collaborate with internal teams (Business Unit, Operations, Engineering) to achieve company goals and objectives
    Ensure the Quality Operations team achieves appropriate levels of compliance and develops actions to ensure ongoing performance is achieved and maintained through metrics and other forms of KPIs
    Establish policy throughout the commercial manufacturing enterprise for adherence to FDA, EMA, ANVISA, and all other relevant government agencies
    Provide management over the Quality Business Unit teams
    Responsible for Deviation Management processes
    Partner with internal teams (Business Unit, Operations, Engineering) to achieve company goals


    Experience/Qualifications:
    Bachelor's or Master's degree in a relevant life-science field
    Minimum of 5+ years of operational quality and manufacturing experience in pharmaceutical or biotech industries
    Proven leadership experience in managing Quality teams with product release responsibilities
    Experience in managing drug/device combination products, preferably with expertise in auto-injection technologies
    Strong understanding of regulatory requirements for pharmaceutical and biotech products, including FDA, EMA, etc
    Excellent communication skills with the ability to interact effectively with internal and external stakeholders
    Prior experience in managing contract service providers or working in a contract manufacturing or contract packaging environment is advantageous


    Apply:
    The Global Life Science Hub are a niche Life Science headhunting firm.

    We place professionals across Europe and the US for a variety of Biotechnology, Pharmaceutical and CRO companies ranging from small start-ups to large global organisations.

    If you're interested, please apply below. If this position doesn't interest you, please visit our website for a list of more vacancies -
    #J-18808-Ljbffr


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