I am recruiting for a Director, PV QMS (Quality Management System) with a stable biotech who has multiple marketed medicines, a premier late stage pipeline and has been leading their industry for 20+ years. This position involves overseeing all activities related to the Pharmacovigilance Quality Management System, ensuring audit and inspection readiness globally.
Key responsibilities include:
- Leading Compliance & Training within the Safety/PV team and cross-functionally to drive global compliance.
- Providing strategic input and tactical implementation for Pharmacovigilance activities and projects.
- Identifying and communicating compliance risks and overseeing action plans to mitigate those risks.
- Leading and developing operational excellence in corrective and preventative action deliverables to ensure timely compliance.
