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

EU & UK QPPV Responsibilities:Oversee AstraZeneca's PV system to ensure compliance with EU/EEA and UK legal requirements and Good Pharmacovigilance Practice (GVP).Ensure the quality, correctness, and completeness of key pharmacovigilance activities and outputs, for example Product Information, Risk Management Plans, Periodic Reports, Health Authority Queries and emerging safety concernsAct as a PV contact point for regulatory authorities on a 24-hour basis.Head of Pharmacovigilance Excellence:Lead the Pharmacovigilance Excellence team to ensure and enhance the quality and compliance of the global PV systemProvide cross-functional expert Pharmacovigilance knowledge and maintain best practices across global and local networks.Contribute to the development and implementation of GPS strategy as part of the Patient Safety Leadership team.Build and sustain external relationships with regulatory authorities and partners to establish AstraZeneca's Global Patient Safety (GPS) as industry-leading.

Education, Qualifications, Skills, and Experience

Essential:

Medical degree or Master’s degree in a relevant life science discipline.

Extensive experience in pharmacovigilance/patient safety

Appropriate 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-2025

Closing Date

29-Sept-2025

AstraZeneca 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.