Key ResponsibilitiesYou will support the intake, review, processing, and reporting of Individual Case Safety Reports (ICSRs) from clinical and post-marketed sources.You will help ensure compliance with Good Pharmacovigilance Practice (GVP), AstraZeneca procedures, and local health authority requirements.The role also includes supporting regulatory authority queries, reconciliations, literature and database screening where required, quality and compliance activities, audit and inspection readiness, documentation and archiving, and collaboration with internal teams, service providers, and other external stakeholders.What We're Looking ForWe are seeking a candidate with:A degree in Pharmacy, Medicine, or a Science-related fieldKnowledge of pharmacovigilance and health authority regulationsStrong attention to detail and problem-solving skillsExcellent written and verbal communication skillsA collaborative, cross‐functional working styleFluency in EnglishExperience with vendor management...