Experience in granulation, compression, capsule & coating oral liquid manufacturing areas of regulated markets. FDA approved personnel in tablet manufacturing would be preferred.
Perform accurate Book-in and data entry ICSRs into safety databases within defined timelines. Ensure compliance with regulatory guidelines, SOPs, and company quality standards for PV processes.
Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives. Prior experience with Data Management.