QC team lead

An exciting opportunity has arisen for an experienced Quality Control professional to join a growing, internationally recognised pharmaceutical manufacturing organisation. This role offers the chance to lead a team of QC analysts while playing a key role in maintaining the highest standards of quality, compliance, and continuous improvement within a GMP-regulated environment. As QC Team Leader, you will provide both technical and people leadership, ensuring the efficient operation of the laboratory and supporting the delivery of high-quality products to global markets. Key Responsibilities Lead, coach, and develop a team of QC analysts, driving engagement and performance. Oversee day-to-day laboratory operations and ensure timely completion and approval of testing activities across raw materials, in-process samples, finished products, stability studies, and validation samples. Champion a strong culture of Health & Safety, Quality, and Continuous Improvement. Support the management and closure of CAPAs, deviations, change controls, audit actions, SOP updates, and method revisions. Ensure laboratory systems and processes remain compliant with GMP, GLP, and Data Integrity requirements. Manage laboratory planning and scheduling activities, ensuring priorities and timelines are met. Participate in client and project meetings, providing technical expertise and operational support. Maintain effective stability programmes and associated documentation. Drive process improvements to enhance laboratory efficiency and customer service. Ensure departmental KPIs across Quality, Customer Service, HSE, Stability, and Financial performance are achieved. You will bring a strong background in Quality Control within a pharmaceutical, life sciences, or similarly regulated environment and possess a passion for developing people and driving quality excellence. Requirements Bachelor's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline (or equivalent experience). Proven experience leading and developing QC teams within a GMP-regulated environment. Strong knowledge of pharmaceutical regulations and quality systems. Experience with analytical chemistry techniques and chromatography systems/software. Expertise in analytical method development, transfer, and technical documentation. Excellent communication, stakeholder management, and problem-solving skills. Strong organisational skills with the ability to manage multiple priorities. Proficiency in Microsoft Office, particularly Excel. A collaborative and solutions-focused approach with a continuous improvement mindset