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SRG

Quality Director

SRG Skipton
32 - 40 hour


Show Recently closed jobs

    SRG

    Quality Director

    SRG Skipton
    32 - 40 hour
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Salary
    Hours
    32 to 40 hours per week
    Employment type
    permanent

    Job description

    Site Quality Director - North Yorkshire

    Pharmaceutical / GMP Manufacturing

    A leading GMP manufacturer in North Yorkshire is seeking to appoint a Site Quality Director. This is a senior leadership role with responsibility for site-wide quality operations, regulatory compliance, and strategic development of quality systems within a regulated pharmaceutical manufacturing environment.

    The Role

    Reporting at site leadership level, you will oversee Quality Control, Quality Assurance and Qualified Person activities, ensuring compliance with UK, EU and FDA cGMP requirements. You will lead the development and execution of the site quality strategy, embedding robust systems and driving continuous improvement across all quality functions.

    Key responsibilities include:

    Leading and developing multi-disciplinary quality teams across QA, QC and QP functions
    Designing and implementing a sustainable site quality strategy aligned to business objectives
    Ensuring full compliance with GMP standards and regulatory expectations (UK, EU, FDA)
    Managing quality risk, driving performance improvement, and monitoring KPIs
    Acting as the primary contact for regulatory bodies, audits and inspections
    Supporting cross-functional collaboration, supplier and customer quality activities
    Mentoring and developing the quality team to build capability and succession

    Candidate Profile

    Our client is looking for an experienced quality leader with a strong background in pharmaceutical manufacturing environments.

    You will bring:

    A degree in Chemistry or a related scientific discipline
    Extensive experience in pharmaceutical quality systems and GMP compliance
    Proven track record managing audits, inspections and regulatory interactions
    Strong working knowledge of manufacturing, packaging, testing and distribution processes
    Experience across key quality activities including investigations, change control and batch review
    Leadership capability with the ability to influence across functionsGuidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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