Descripción de la oferta
LQPPV Consultant¿Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar".Location- SpainStart Date- ASAPProject- 12 months project with 2 hours per month- You need to be set up as an autonomo for this roleClient- A Global Pharmaceutical ClientWe'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.This 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.What You'll DoServe as the designated QPPV for EU/UK market authorisationsMaintain full oversight of the PV system and PSMF, ensuring inspection readinessMonitor product safety profiles, lead signal management, and guide benefit–risk decisionsOversee AE case management, compliance metrics, PSURs, RMPs, and safety deliverablesAct as the main contact for health authorities and internal/external partnersSupport audits, inspections, and continuous improvement of PV processesProvide leadership to PV teams and ensure robust PV training across the organisationWhat You BringDegree in Life Sciences, Pharmacy, or Medicine5+ years in PV, ideally with QPPV or Deputy QPPV experienceDeep knowledge of EU GVP, ICH guidelines, and xcskxlj global PV regulationsStrong communication, leadership, and decision-making skillsAbility to manage complex safety issues with clarity and scientific rigorFluency in English; additional European languages are a plusWhy This RoleHigh-impact leadership position at the core of patient safetyOpportunity to shape a global PV system within a collaborative, science-driven environmentCompetitive package and long-term growth potential
