Dublin – Responsibilities: Manage delegated tasks from QPPV on a defined and ad hoc basis with the flexibility of mind-set and time resource this entails. This will include representation at meetings when required. Review, advise and approve relevant local and global guidelines, policies, internal procedures and SOPs. Support Risk Management Plans (RMPs) by serving as a coordinator for the acquisition and preparation of data for review from multiple sources Collect and/or organize the data as part of Pharmacovigilance, RMP, product recalls and surveillance activities Manage outsourced data collection, organization preparation with vendors as required Provide support to related PV activities such as preparation of reports for surveillance support, collating reports for review of product quality data, support of health hazard evaluations, scientific presentations etc. Participate in preparation of analysis and writing of ad-hoc and aggregate regulatory reports and labelling support docum… – Permanent – Full-timeApply for this job.