QA Specialist

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QA SpecialistI am currently working with an exciting Biotech in Scotland's Central Belt. We are looking for a QA Specialist to join the team on a permanent basis. As QA specialist, you will focus on the document review and approval, tracking and closure of Quality Events/Deviations, Change Controls, Environmental Monitoring excursions and Out of Specifications.In addition, the post holder will assist in vendor approval, audits and review of validation documentationResponsibilities:Maintaining/updating and tracking tools and indices to ensure proper monitoring, tracking and closure of all Quality events/Deviations / Change controls / EM Excursions / Out of SpecificationsCo-ordinating corrective and preventative actions resulting from Quality InvestigationsReview and approval of controlled documentsReview and approval of Batch manufacturing records and quality workbooksReview and approval of protocols and reportsCo-ordinating change control and deviations meetings.Requirements:Minimum of 3 year's experience working in a similar GMP environmentExperience of quality systems including change control, deviations and CAPA managementExperience of vendor assurance or GMP equipment/facility validation would be desirableIf this Quality Specialist position looks like it could be the next step in your career, please get in touch ASAP! 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