Are you passionate about ensuring excellence in aseptic quality and stability within the pharmaceutical industry? Do you have the expertise to oversee clinical dimensions, regulatory compliance, and drive innovation in compounded medication protocols? If so, we have an exciting opportunity for you! Key Responsibilities In this influential role, you will: Ensure Compliance:Maintain the highest standards of patient safety and product quality by ensuring all aseptic processes and compounded medications comply with UK regulatory standards, including Yellow Cover Documents (YCD), MHRA guidelines, and Good Manufacturing Practice (GMP) Drive Efficiencies: Review, update, and enhance stability protocols, prescription processes, and associated standards for compounded medications to ensure safe, effective, and patient-centred outcomes. Innovate: Lead research and development initiatives to advance compounded medication stability and implement innovative practices. Quality Assurance:Deliver a robust pharmacy quality assurance framework by conducting risk assessments, managing incidents and non-conformances, and driving continuous improvement. Build Capability:Act as the subject matter expert, providing guidance and training to colleagues and customers on aseptic quality and stability. Foster Relationships:Work closely with internal stakeholders to deliver the highest standards of service, support commercial opportunities, and build customer relationships.