Pharmacovigilance QA Manager
- Interim/Contract
- PVG & Drug Safety, Clinical Drug Safety
This vacancy has now expired. Please see similar roles below...
Hobson Prior is seeking a Pharmacovigilance QA Manager. This role involves ensuring the implementation of a standardized Pharmacovigilance (PV) system, maintaining relationships with internal stakeholders, and overseeing a global PV QA audit program.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Act as the local PV QA Manager, ensuring the implementation of a standardized PV system.
- Be the primary contact for internal stakeholders, providing expert-level PV knowledge and guidance.
- Maintain and improve a risk-based, global PV QA audit program.
- Conduct PV QA audits of vendors and maintain oversight of QA consultants.
- Escalate significant PV compliance issues to senior management.
- Review procedures for CAPA and deviation management, root cause analysis, and perform QA effectiveness checks.
Key Skills & Requirements:
- Expert knowledge of international Pharmacovigilance regulations.
- Experience in training employees on GVP requirements and pharmaceutical industry practices.
- Experience in QA/industry/health authority, including the conduct of PV audits.
For more information, please contact William Tyler.
Apply now
If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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