Location: Didcot, Oxfordshire
Develop and maintain robust QC processes as required and in compliance with regulatory and clients requirements.
Support the quality and business management teams during management reviews with clients by monitoring and reporting KPIs status.
Comply with QA processes and requirements within the QC department
SOP writing, CAPA management, change control, training, internal audits, etc.
Co-host regulatory and client's audits in conjunction with the quality management team, aiming at eliminating risk of findings during audits and raising and closing appropriate CAPAs to address any audit observation.
6 months to 1 year's experience in QC roles within the pharmaceutical industry.
Diploma/Certificate on quality and/or related life science subject.
Flexibility to work in any of the sites within the campus at short notice
Analytical and good at paying attention to detail.
IT literate - intermediate level with MS Office packages such as Word, Excel and Power Point.
Proactive, task orientated and good at completing tasks and meeting targets in a timely manner.
Good understanding of GMP/GDP requirements.
Please contact Ruth on for further details.
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