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SRG

Senior QC Scientist

SRG Gatley
32 - 40 hour


Show Recently closed jobs

    SRG

    Senior QC Scientist

    SRG Gatley
    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

    Senior QC Scientist

    Greater Manchester

    SRG are recruiting for a Senior QC Scientist to join a highly successful CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all the way through early-stage trials and to approval.

    Due to continued growth and expansion of the business they are seeking to hire a Senior QC Scientist to join their team in Greater Manchester to lead hands on QC testing, ensure the GMP compliance of finished products and support ongoing development & continuous improvement of QC Systems, methods and regulatory readiness.

    Key Responsibilities

    Perform analytical testing including:
    HPL / UHPLC (Assay, Related substances & Cleaning verification methods)
    Dissolution Testing inc. method transfers, validations and troubleshooting.
    Compendial techniques - FTIR, pH, content uniformity, water content etc.
    Ensure compliance with GMP and regulatory standards, supporting audit and inspection readiness
    Write and review:
    Analytical methods and validation documentation
    SOPs and laboratory quality documents
    Certificates of Analysis and technical reports
    Manage stability studies from initiation through to reporting, including third-party liaison
    Support onboarding and lifecycle management of QC instrumentation (IQ/OQ/PQ)
    Supervise and mentor junior scientists, including training and competency sign-off
    Contribute to continuous improvement initiatives, including lean QC processes
    Support QC planning, laboratory organisation, and resource allocation

    Required

    A degree or comparable experience in Chemistry, Pharmaceutical Sciences, Biochemistry, or similar relevant field.
    Proven QC / analytical experience within a similar GMP environment.
    Skilled in the operation of HPLC / UHPLC, FTIR and similar techniques.
    Experience with method validation, transfer, and technical documentation
    Good understanding of regulatory frameworks (e.g. EU GMP, ICH guidelines)
    Exposure to stability studies and data trending would be advantageous
    Previous experience mentoring or supervising colleagues is desirableGuidant, 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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