Senior QA Associate

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Role OverviewWe are currently looking for a Senior QA Associate to join a growing biotechnology company based in Stevenage. As the Senior QA Associate you will be responsible for supporting the manufacturing and release of products under the QMS environment, support product and batch record reviews, investigations into non-compliance and CAPA Management.Duties and Responsibilities Maintain quality supporting documentation to facilitate GMP ProductionWrite and review quality SOP's and associated documentation for GMP productionCarry out investigations for deviations and non-conformances.Support MHRA licensingRelease documents and labels to the manufacturing production teamsReview change controls records impacting productsImplement CAPAs to improve product quality Education and ExperienceWe are looking to identify the following in your profile:Degree or Masters in a relevant scientific discipline and a number of years of GMP industry experience within a biotech, biologics or similar organisation.MHRA licensing experience is essential to your applicationPrevious industry experience using QMS including implementation and development. To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales