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Smart4Sciences

Document Manager, Pharmaceuticals (Contract, Outside IR35)

Smart4Sciences Crewe
32 - 40 hour


Show Recently closed jobs

    Smart4Sciences

    Document Manager, Pharmaceuticals (Contract, Outside IR35)

    Smart4Sciences Crewe
    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
    contract

    Job description

    Document Manager - CAPEX Projects (Pharmaceutical Industry) Contract, Outside IR35

    We are seeking an experienced and detail-oriented Document Manager to support CAPEX (Capital Expenditure) projects within a dynamic pharmaceutical environment. This role is critical in ensuring the effective control, organization, and compliance of project documentation across all phases of delivery.

    Key Responsibilities:

    Establish and maintain document control systems for CAPEX projects, ensuring accuracy, version control, and accessibility.
    Manage the lifecycle of engineering, construction, and validation documents in line with regulatory and company standards.
    Coordinate with project managers, engineers, contractors, and quality teams to ensure timely submission, review, and approval of documents.
    Ensure compliance with industry regulations (e.g GMP) and internal quality management systems.
    Track document status, generate reports, and support audits and inspections.
    Implement and improve document management processes and tools to enhance efficiency.Key Requirements:

    Proven experience in document control or document management within pharmaceutical, life sciences, or highly regulated industries.
    Familiarity with CAPEX project environments (engineering, construction, commissioning).
    Strong understanding of document control systems and electronic document management systems (EDMS).
    Knowledge of regulatory requirements such as GMP and data integrity principles.
    Excellent organizational, communication, and stakeholder management skills.
    High attention to detail and ability to manage multiple priorities under tight deadlines.Desirable:

    Experience supporting large-scale pharmaceutical or biotech facility projects.
    Familiarity with validation documentation (IQ/OQ/PQ) and quality systems.
    Degree or relevant qualification in a technical or business-related discipline.What We Offer:

    Opportunity to work on high-impact CAPEX projects in a regulated, innovative industry.
    Collaborative and professional work environment.
    Competitive salary and benefits package.If you are a proactive and structured professional with a passion for document excellence in complex project environments, we would like to hear from you
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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