Senior Director of Quality Assurance in Pharmacovigilance and Life-Cycle Management

1 week ago


London, Greater London, United Kingdom GSK Full time

GSK offers a unique opportunity to join a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together.

Job Overview:

The Senior Director Quality Business Partner: Pharmacovigilance and Regulatory role plays a critical part in developing and delivering quality strategies in Pharmacovigilance and Lifecycle Management, ensuring regulatory compliance and patient safety.

This position requires a strong leader who can manage a small team of Quality Business Partners and provide assurance to GSK R&D senior management that GSK processes for managing safety data are effective.

Responsibilities:
  • Develop and implement the quality strategy for Pharmacovigilance and Lifecycle Management activities.
  • Manage a small team of Quality Business Partners to ensure successful delivery of quality initiatives.
  • Collaborate with cross-functional teams to identify and mitigate risks associated with Pharmacovigilance and Lifecycle Management activities.

Key Skills Required:

  • Bachelor's degree or equivalent in scientific or quality-related field.
  • Proven experience in drug development, pharmacovigilance operations, regulatory compliance or quality management.
  • Strong knowledge of GCP, pharmacovigilance/drug safety and regulatory requirements.

The estimated salary for this position is approximately £100,000 per year, based on industry standards for similar roles in the UK area.



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