Teams at AstraZeneca

Provide SME support for contamination control and environmental monitoring in GMP radioconjugate manufacturing. Design and maintain EM programs, lead EMPQ studies, assess excursions, drive investigations and CAPA, author GMP documentation, advise on bioburden control, support cleanroom qualification, and train cross-functional teams to ensure regulatory compliance and product quality.

Lead site QA/QC and compliance for radiopharmaceutical manufacturing, ensuring cGMP adherence, inspection readiness, product release, CAPA management, quality metrics, continuous improvement, and development of quality staff and processes.

Lead and oversee global haematology clinical studies from protocol development through archiving. Coordinate cross-functional and external partners (CROs, vendors), ensure study materials and IP supply, support budget and project management, maintain inspection-ready documentation and safety reporting, monitor study progress and risks, and assist in meetings and study document preparation to deliver studies on time, budget, and quality.