Do you want to be involved in supporting the development of cutting-edge and breakthrough therapies? A steadily growing CDMO have opportunity for an experienced QA officer to join them on-site on a permanent basis. What you’ll be doing Writing and reviewing quality documents, SOPs and other policies Supporting with QMS activities including issuing validation plans and performing risk assessments Support all departments with writing and assessing change controls, non-conformances, root-cause analysis, risk assessments and CAPAs Support with internal and external audits and other regulatory inspections Develop and implement training materials and sessions in-house What we need from you Proven experience in cellular and/or gene therapies working in a QA role, preferably within a GMP environment Experience in writing QA documents, particularly SOPs Experience performing and managing risk assessments Experience with internal auditing as well as managing deviations, non-conformances and CAPAs Understanding of cell and gene therapies A BSc in life sciences, or comparable experience What’s on offer Competitive salary Additional benefits Excellent opportunities for growth and personal development Progression opportunities