Senior Director, Deputy Qppv

Trzdev37

Not specified
Pharmacovigilance data quality oversight
Product safety and risk management
Regulatory submissions and documentation review
The Senior Director, Deputy QPPV role at Trzdev37 involves overseeing pharmacovigilance responsibilities, supporting regulatory submissions, and ensuring product safety and risk management. The position requires extensive experience in the pharmaceutical industry and a scientific or medical degree, with a strong emphasis on compliance and quality improvement in patient safety processes

Job Summary

  • The Senior Director QPPV deputises for the EU Qualified Person for Pharmacovigilance (QPPV), assuming QPPV responsibilities during their absence.
  • Core accountabilities include oversight of pharmacovigilance (PV) data quality, product safety and risk management, involvement in regulatory submissions and documentation review and approval and the promotion of quality and compliance across patient safety team.
  • AstraZeneca embraces diversity and equality of opportunity and is committed to building an inclusive and diverse team representing all backgrounds.

Matching Summary

Match Score: 85

The Senior Director, Deputy QPPV role at Trzdev37 involves overseeing pharmacovigilance responsibilities, supporting regulatory submissions, and ensuring product safety and risk management. The position requires extensive experience in the pharmaceutical industry and a scientific or medical degree, with a strong emphasis on compliance and quality improvement in patient safety processes.

Skills & Requirements

Must-have

  • pharmacovigilance data quality oversight
  • product safety and risk management
  • regulatory submissions and documentation review
  • EU QPPV responsibilities
  • patient safety team promotion

Nice-to-have

  • embraces diversity and equality
  • inclusive and diverse team
  • harnessing industry-leading skills
  • continuous improvement within PV processes

Key Requirements

  • Scientific or Medical degree
  • Sufficient basic medical knowledge
  • Extensive pharmaceutical industry experience
  • Detailed understanding of PV legislation
  • Awareness of current pharmaceutical industry developments
  • Excellent communication skills
  • Project management experience
  • Residency within the EU

Work Rights

Residency within the EU

Tailored Resume

Cover Letter