Sr. QPPV Office (QPO) Specialist job opportunity at Biomapas.

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Date2026-01-19T13:21:37.666Z bot
Biomapas Sr. QPPV Office (QPO) Specialist
Experience: 4-years
Pattern: Full-time
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Lithuania

Join our global Pharmacovigilance team as a Sr. QPPV Office (QPO) Specialist. Sr. QPPV Office (QPO) Specialist is responsible for the development of pharmacovigilance systems, and the oversight of end-to-end pharmacovigilance activities and projects’ compliance with Quality Management System as well as the reporting and exchanging of safety and pharmacovigilance information for medicinal products. Position is in any EU country. Responsibilities: Manage full Pharmacovigilance systems and projects (or part of them) Promote, maintain, improve compliance with Pharmacovigilance (PV) tasks and responsibilities May act as Regional QPPV or deputy Influence the performance of the quality system and PV activities Develop, update, and review standard operating procedures for global pharmacovigilance processes, and implement changes to fulfill requirements Supervise, prepare and submit PSURs, Risk Management Plans and risk minimization activities Be the primary point of contact for PV-related matter Ensure oversight of the contractual partner safety data exchange agreements Ensure the survey and monitoring of European (including UK) level pharmacovigilance regulations Provide Pharmacovigilance trainings Ensure continuous safety profile monitoring, detection of new signals and evaluation Communication with Competent Authorities Participate in related inspection and/or audits University degree in Life Science field At least 4 years of experience in pharmacovigilance roles, including in-depth, demonstrated experience in most areas pertaining to pharmacovigilance, and expert knowledge of pharmacovigilance legislation Experience in regional QPPV role and risk minimization activities will be considered as an asset Experience in Pharmacovigilance Medical writing Strong computer literacy with intensive experience with safety databases Ability to interpret and apply global drug safety regulations Fluent English language Good knowledge of medical terminology Attention to detail, time-management and problem-solving skills Proficient knowledge in MS Office

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