Respond to and action quality enquiries and quality management activities including deviations, change controls, risk assessments, complaints etc. Author, review and archive quality documentation including SOPs, PQRs, supplier agreements. Ensure GMP/GDP compliance at all times. Key Requirements
Prior GMP experience within the pharmaceutical/medical device industries is essential. Prior experience working with Pharmaceutical Quality Management Systems is essential. A pro-active, can do attitude is essential. Interviews for this QA Officer position are imminent so please apply now or contact Gareth Gooley at Smart4Sciences for more information.
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