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    Quality Control Analyst - Liverpool, United Kingdom - Russell Tobin

    Russell Tobin
    Russell Tobin Liverpool, United Kingdom

    3 weeks ago

    Default job background
    Pharmaceutical / Bio-tech
    Description
    Quality Control Analyst – 9 months contract – Liverpool - £18.50 per hour Umbrella - Biotechnology company

    Overview:

    nSupports the QC Compliance and Improvement Manager in providing compliance support across QC activities.nInitiate innovations and improvement projects across QC and be involved with their execution and timely completion.nParticipate in site improvement project teams, drive quality decisions, and provide advice and technical support where required.nYou will deal with internal and external contacts.nInternal contacts – Data inputs from Supply Chain, Operational Teams, and Project and AS&T teams, which must be reviewed and interpreted to maximise laboratory resources in line with site objectives.

    Works closely with the QC Managers, QC labs, and SME's.nExternal contacts- Global Quality Systems and Compliance for changes in Health Authority expectations.

    Daily interaction with VWR who manage site consumables and reagents via in-plant personnel.

    Responsibilities:

    nWork closely with the labs to lead Deviations, CAPA's, and Change Controls through to on-time completion.nParticipate in lab improvement projects.nTo ensure appropriate standards of cGMP, Housekeeping, Health, Safety and Environment are applied in all activities, in accordance with current regulations and procedures.nEnsure QC compliance with Company PoliciesnSupport QC labs with respect to sample delivery from across the Liverpool sites to the labs in a timely manner.nKeep oversight of and facilitate on time completion of DR's, CAPA's, Change Controls and SOP UpdatesnMonthly and annual report writing for EM, Bioburdens and Endotoxin results, including annual product review.nTo collate data relating to site and organisational changes that will impact the efficient running of the laboratories.nManage the completion of DR's, CAPA's, Change Controls and SOP updates working closely with the QC labs.nAttendance at and presentation at DRB.nCAPEX project submissions and management.nInvalid reporting.nMaintenance of QC metrics.nPPS problem-solving.


    Must haves:

    ncGMP background in the Pharmaceutical industrynExperience of Quality Control / Microbiological testing techniques and industry practicesnKnowledge and understanding of Lean Lab principles.nGood understanding of the QC labsnKnowledge of continuous improvement techniques and advanced root cause analysis techniquesnReport writing skills.nProven time management skillsnProven communication skills both written and verbal.

    nAcademically trained to a minimum of degree standard in a relevant scientific discipline
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