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Smart4Sciences

QA Officer

Smart4Sciences Knutsford
32 - 40 hour


Show Recently closed jobs

    Smart4Sciences

    QA Officer

    Smart4Sciences Knutsford
    32 - 40 hour
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Hours
    32 to 40 hours per week
    Employment type
    permanent

    Job description

    We are currently recruiting for a Quality Assurance Officer to join a fast-paced pharmaceutical manufacturing organisation committed to delivering high-quality, safe, and compliant products including unlicensed medicines and NHS-approved disinfectants.

    This is a key role within the QHSE department, supporting the ongoing development and maintenance of a robust Quality Management System (QMS) in line with GMP, ISO 9001, and ISO 14001 standards.

    About the Role

    As a Quality Assurance Officer, you will play a critical role in ensuring product quality, regulatory compliance, and continuous improvement across the site. You will work closely with cross-functional teams including production, QC, and technical departments to maintain high standards of compliance and operational excellence.

    You will be involved in document control, deviation management, CAPA systems, internal audits, and regulatory inspection support, helping to drive a strong culture of quality and accountability.

    Key Responsibilities

    Support the maintenance and continuous improvement of the Quality Management System (QMS)
    Review, author, and update SOPs, specifications, and controlled documents
    Manage deviations, CAPAs, change controls, OOS/OOT investigations, complaints, and recalls
    Support and participate in internal and external audits
    Assist in preparation for regulatory inspections (e.g. MHRA, ISO audits)
    Maintain training records and site-wide training matrices
    Support quality metrics, KPI reporting, and trend analysis
    Ensure accurate document control, archiving, and compliance systems
    Contribute to continuous improvement initiatives across the business

    Essential

    A degree in a scientific or related discipline, or equivalent relevant industry experience
    Strong working knowledge of Good Manufacturing Practice (GMP) within a regulated environment
    Hands-on experience with Quality Management Systems (QMS)
    Practical experience in key QA processes including document control, deviations, CAPA, and change control
    Experience supporting or preparing for internal and external audits / regulatory inspections

    Desirable Experience

    ISO 9001 / ISO 14001 exposure
    Internal auditing experience
    GMP/QMS auditing certification
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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