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Auditor - GVP

Company

CSL

Location

Maidenhead, England

Type

Full time

Quality in a globalized drug safety network is a matter of operational resilience as much as regulatory mandate. This role serves as aGVPAuditorwithin our Research & Development Quality audit program, responsible for executing the global audit plan to ensure the accuracy of safety data and compliance with legal and corporate standards. By conducting audits of our external partners and internal safety functions, you identify the findings and non-compliance trends that couldimpactthe reliability of our pharmacovigilance system. We are looking for an experienced auditor who can navigate complex safety environments and work collaboratively with stakeholders to develop corrective actions that ensure long-term systemic stability.

Main Responsibilities

  • Audit Execution:Conduct assigned external audits of pharmacovigilance vendors and service providers, as well as internal self-inspections of safety processes,systems, andaffiliates(including Local/Regional S...
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