QPPV Consultant

LQPPV Consultant Location - Spain Start Date- ASAP Project - 12 months project 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. You will be working closely with cross-functional teams to identify and mitigate potential risks, ensuring that all PV activities are conducted in accordance with relevant regulations and guidelines. Your expertise will be instrumental in maintaining a robust and compliant PV system, which will enable us to make informed decisions about our products and ensure the well-being of patients worldwide. If you have a strong background in Pharmacovigilance and a passion for ensuring patient safety, we encourage you to apply for this exciting opportunity.