LQPPV Consultant
Location - Spain
Start Date- ASAP
Project - 12 months rovject with 2 hours per month
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