Overview Zambon is seeking a Pharmacovigilance Agreement Senior Specialist to join its Drug Safety Unit.ResponsibilitiesPreparation, review, and maintenance of Pharmacovigilance Agreements (PVAs) with Zambon business partners (including distributors, licensees, licensors) and affiliates, in accordance with Zambon standard procedures and applicable regulations.Assist in the development and update of relevant procedures, PV agreement templates and pharmacovigilance clauses to ensure consistency and regulatory compliance.Collaborate with the management of Zambon EU, UK Pharmacovigilance System Master Files (PSMFs), and other national PSMFs, ensuring alignment and consistency with the EU PSMF.Support the monitoring of key performance indicators of the PV system.Supports QPPV to ensure adequate and continuous oversight of the Zambon Pharmacovigilance System quality and performance.Support audits and inspections, contributing to, and monitoring of, corrective and preventative actions related to the PV system performance.What we are looking forBachelor’s degree in Pharmaceutical Chemistry, Physical Sciences, or a related scientific discipline.A minimum of 5-year experience in the pharmacovigilance department of pharmaceutical companies or healthcare organizations.Experienced in operational, pharmacovigilance procedures and regulations, with particular emphasis on EU regulations. Knowledge of quality assurance basics preferred.Good knowledge of English language.Strong knowledge of PV legislation and guidelines.Project Management capabilities/organizational skills.Ability to collaborate effectively with internal teams and external business partners.IT Tools (Microsoft Office tools).Seniority levelMid-Senior levelEmployment typeFull-timeJob functionOther and ScienceIndustriesPharmaceutical Manufacturing
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