About the Opportunity A leading global pharmaceutical organisation is seeking a Quality Assurance Specialist to join their UK-based team. This company is committed to regulatory excellence and continuous improvement in the commercialisation of medicinal products. With a strong international footprint and a focus on high-quality standards, they collaborate closely with health authorities, contract manufacturers, and internal stakeholders to ensure compliance across the product lifecycle. Key Responsibilities Lead product release and compliance activities, ensuring documentation accuracy and adherence to GMP/GDP standards. Maintain and improve Quality Systems including Change Control, Deviations, Complaints, Product Quality Reviews (PQRs), Recalls, and Returns. Act as a key liaison with Health Authorities, ensuring timely incident reporting and regulatory compliance. Conduct risk assessments, support technical knowledge-sharing, and contribute to quality documentation. Implement and monitor Corrective and Preventative Actions (CAPAs), track effectiveness, and report outcomes to senior leadership. Drive continuous improvement initiatives to enhance operational quality and efficiency. What You'll Bring A degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Biochemistry, or a related discipline. 5 years' experience in Quality Assurance, Quality Control, or a similar function within the pharmaceutical or healthcare sector. Certifications in GMP and GDP. Strong knowledge of regulatory affairs, pharmaceutical guidelines, and quality systems. Proven experience in compliance activities including CAPAs, Change Control, and Deviations. Exposure to regulatory audits and interactions with Health Authorities is highly desirable. A proactive mindset with a passion for quality improvement and operational excellence. Why Apply? Join a global leader in pharmaceutical innovation. Work in a collaborative and quality-driven environment. Be part of a team that values regulatory integrity and continuous improvement.