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SRG

QC Bioassay Analyst

SRG Liverpool
32 - 40 hour


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    SRG

    QC Bioassay Analyst

    SRG Liverpool
    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
    temporary

    Job description

    An exciting opportunity has risen for a QC Analyst to join a global pharmaceutical company within their bioassay lab, within QC.

    Job Title: QC Bioassay Analyst

    Vacancy type: Temporary role expected to last around 6 months (5 on 3 off shift pattern)

    Area: Liverpool

    Salary: Highly competitive

    SRG is working with a leading global pharmaceutical company who require a QC Bioassay Analyst to join their well-established QC lab. The purpose of the QC Bioassay analyst role is to compliantly perform QC laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs). Analysis is performed on in-process, intermediate and finished vaccine products. QC Bioassay analysts are also required to participate in technical and validation studies in support of both departmental and site objectives.

    Responsibilities:

    The purpose of the QC Incoming and Components Analyst role is to compliantly perform Primary QC inspection, Sampling of raw materials, components laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs) for all primary and secondary packaging components.
    QC Incoming and components analysts will be required to support release of raw materials and components for use in manufacture. QC incoming and component's Analysts may also be required to participate in technical and validation studies in support of both departmental and site objectives.
    Work to a high level of cGMP and GDocP in order to maintain compliance and adherence to regulations.
    Perform analytical testing of raw materials, in process, finished product and utilities samples in accordance with relevant SOPs.
    Instrument Maintenance and Calibration
    Escalate any OOS/OOE/OOT results to Team Co-Ordinator/Laboratory Manager as soon as practically possible.
    Initiate and perform laboratory investigations with discussion and collaboration with effected departments where necessary.

    Applicant requirements:

    BSc in equivalent in Scientific discipline, ideally chemistry.
    Recent experience in a cGMP pharmaceutical lab performing analytical QC bioassay testing for at least 1 year.

    SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

    As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

    If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) view our other vacancies.

    Guidant, 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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