QPPV and Head Pharmacovigilance Excellence
AstraZeneca
As the European Union (EU) and United Kingdom (UK) Qualified Person for Pharmacovigilance (QPPV), you will be accountable for AstraZeneca’s compliance with EU/EEA and UK regulatory requirements governing pharmacovigilance activities. Additionally, you will lead the Pharmacovigilance Excellence team to ensure the optimal quality and compliance of the AZ Pharmacovigilance (PV) System globally.Key Responsibilities
Education, Qualifications, Skills, and ExperienceEssential:Medical degree or Master’s degree in a relevant life science discipline.Extensive experience in pharmacovigilance/patient safetyAppropriate experience of acting as EU QPPV/Deputy QPPV, preferably in large or mid-size pharmaceutical company.Excellent communication and influencing skills.Desirable:Expert reputation within the business and industry.PhD in a scientific discipline.Knowledge of technology development within the PV area.Key Relationships:Internal: Deputy EU QPPVs, GPS TA product teams, Chief Safety Officer, Chief Medical Officer, Regulatory Affairs.External: EMA, MHRA, Other regulatory authorities, external PV vendors and industry groups.Date Posted 15-May-2025Closing Date 29-Sept-2025AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
Barcelona
Sat, 17 May 2025 07:08:13 GMT
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