Descripción de la oferta
LQPPV Consultant Location - Spain Start Date- ASAP Project - 12 months project with 2 hours per month- You need to be set up as an autonomo for this role Client - A Global Pharmaceutical Client We’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 Do Serve as the designated QPPV for EU/UK market authorisations Maintain full oversight of the PV system and PSMF, ensuring inspection readiness Monitor product safety profiles, lead signal management, and guide benefit–risk decisions Oversee AE case management, compliance metrics, PSURs, RMPs, and safety deliverables Act as the main contact for health authorities and internal/external partners Support audits, inspections, and continuous improvement of PV processes Provide leadership to PV teams and ensure robust PV training across the organisation What You Bring Degree in Life Sciences, Pharmacy, or Medicine 5+ years in PV, ideally with QPPV or Deputy QPPV experience Deep knowledge of EU GVP, ICH guidelines, and global PV regulations Strong communication, leadership, and decision-making skills Ability to manage complex safety issues with clarity and scientific rigor Fluency in English; additional European languages are a plus Why This Role High-impact leadership position at the core of patient safety Opportunity to shape a global PV system within a collaborative, science-driven environment Competitive package and long-term growth potential
