As Deputy EU QPPV, you act as the designated back-up for the EU QPPV during periods of absence and provide day-to-day operational leadership within the EU QPPV Office. You will influence key safety decisions, guide cross-functional partners, and represent the EU QPPV Office in governance forums—bringing clarity, rigor, and a strong patient-first mindset. * Serve as Deputy EU QPPV in line with EU legislation, applicable EU regulations/directives, and GVP Modules; act as back-up to the EU QPPV as required. * Support critical PV oversight and approvals, including aggregate reports, Risk Management Plans, risk minimisation measures/materials, PASS, responses to regulatory authorities, and the Pharmacovigilance System Master File. * Represent the EU QPPV Office in key internal governance forums (e.g., signal detection and product safety committees) and contribute to core safety information.
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