PLQPPV Consultant /ppbLocation /b- Spain /ppbStart Date- /b ASAP /ppbProject /b- 12 months project with 2 hours per month-b You need to be set up as an autonomo for this role /b /ppbClient /b- A Global Pharmaceutical Client /ppbr/ppWe’re looking for an experienced QPPV to lead and oversee our Pharmacovigilance (PV) system and ensure the highest standards of patient safety and regulatory compliance. In this pivotal role, you will be the key expert responsible for the safety of our marketed products and the integrity of our global PV operations. /ppbr/ppThis is an ad-hoc role of 2 hours per month and you need to already be set up as a freelancer either as an Autonomo or with your own LTD company. /ppbr/ppbWhat You’ll Do /b /pulliServe as the designated QPPV for EU/UK market authorisations /liliMaintain full oversight of the PV system and PSMF, ensuring inspection readiness /liliMonitor product safety profiles, lead signal management, and guide benefit–risk decisions /liliOversee AE case management, compliance metrics, PSURs, RMPs, and safety deliverables /liliAct as the main contact for health authorities and internal/external partners /liliSupport audits, inspections, and continuous improvement of PV processes /liliProvide leadership to PV teams and ensure robust PV training across the organisation /li /ulpbr/ppbWhat You Bring /b /pulliDegree in Life Sciences, Pharmacy, or Medicine /lili5+ years in PV, ideally with QPPV or Deputy QPPV experience /liliDeep knowledge of EU GVP, ICH guidelines, and global PV regulations /liliStrong communication, leadership, and decision-making skills /liliAbility to manage complex safety issues with clarity and scientific rigor /liliFluency in English; additional European languages are a plus /li /ulpbr/ppbWhy This Role /b /pulliHigh-impact leadership position at the core of patient safety /liliOpportunity to shape a global PV system within a collaborative, science-driven environment /liliCompetitive package and long-term growth potential /li /ul