and liaise with Global Regulatory, Regulatory Science/CMC, Supply Chain, Submissions Management, other lifecycle regulatory work, liaising with Regulatory Science/CMC, Submissions Management, Cluster/Markets, and
registration dossiers/ documents. Obtain relevant information from global RA and resolve queries as they arise of registration status & market specific information for accuracy and completeness in the relevant feedback on quality of service and support & information provided. Constructive feedback from regulatory Pharmacist. Experience in eCTD. Expertise in Information and document management technology and electronic/paper including processes and technologies. Expertise in Information and document management technology and electronic/paper