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RBW Consulting

QA Officer

RBW Consulting Stoke-on-Trent
32 - 40 hour


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    RBW Consulting

    QA Officer

    RBW Consulting Stoke-on-Trent
    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

    Quality Assurance Officer
    šŸ“ Pharmaceutical Manufacturing | GMP Environment | Permanent
    Are you a Quality Assurance professional with GMP experience looking to take the next step in your career?
    We're recruiting for a Quality Assurance Officer to join a growing quality team supporting the manufacture, testing, and release of pharmaceutical products within a highly regulated environment.
    This is an excellent opportunity for someone with a strong QA background who enjoys maintaining compliance, driving quality improvements, and working closely with cross-functional teams.
    Key Responsibilities
    * Support the Quality Management System (QMS) and GMP compliance activities
    * Assist with deviations, CAPAs, change controls, and quality investigations
    * Review and maintain GMP documentation, SOPs, and quality records
    * Support validation and qualification activities
    * Participate in internal audits and support regulatory inspections
    * Work closely with Production, QC, and other departments to ensure quality standards are maintained
    * Contribute to continuous improvement initiatives across the quality function
    What We're Looking For
    * Degree in Pharmacy, Chemistry, Biology, or a related scientific discipline (or equivalent industry experience)
    * Experience working in a GMP-regulated pharmaceutical environment
    * Strong understanding of Quality Assurance principles and Quality Management Systems
    * Excellent attention to detail, organisation, and report-writing skills
    * Ability to work independently and as part of a team
    Desirable Experience
    * Sterile manufacturing or injectable products
    * Validation and qualification activities
    * Internal auditing
    * QC or Production experience within pharmaceuticals
    This role would suit a proactive, quality-focused professional who enjoys working in a fast-paced regulated environment and wants to make a meaningful contribution to product quality and patient safety.
    šŸ“© Interested? Apply now or get in touch for a confidential discussion
    Apply now

    Apply on the employer's website

    Apply now

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    Stoke-on-Trent England

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