EU Qualified Person for Pharmacovigilance Leadership Role

5 days ago


Stockholm, Stockholm, Sweden Lilly Full time
Job Summary

We are seeking an experienced EU Qualified Person for Pharmacovigilance to lead our team and ensure compliance with regulatory requirements.

About Us

Lilly is a leading pharmaceutical company committed to improving the lives of people worldwide through innovative medicines and solutions.

Key Responsibilities
  • Deputise for the EU QPPV as required and provide strategic advice to Global Patient Safety and other regulatory functions.
  • Maintain current awareness of the evolving EU regulatory environment and provide timely feedback to GPS leadership.
  • Provide expert input to EU regulatory submissions, PASS protocols, and risk minimisation actions.
  • Fulfill all QPPV obligations as stipulated in the Good Vigilance Practice (GVP) guidelines.
Requirements
  • Medical degree and clinical experience
  • Global focus with residency and operation in the EU/EEA
  • A minimum of 5 years' experience in pharmacovigilance
  • Strong influencing, coaching, and negotiating skills across multiple internal and external audiences
  • Current awareness of product safety regulatory environment
Benefits
  • Average salary: €120,000 per year
  • Excellent company pension plan
  • Professional development opportunities via Lilly University


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