Global GCP Auditor | Data Integrity & CAPA
Listed on 2026-10-07
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Quality Assurance - QA/QC
CSL Vifor is seeking a GCP Auditor to join the R&D Quality audit program, executing the global audit plan to ensure data integrity and compliance with legal and corporate standards. You will audit clinical investigator sites, CROs, and internal trial management processes.
The role requires 3+ years QA in a GCP-regulated environment, strong communication, and travel up to 50%. You will report findings and CAPA, support SOP improvements, and stay current with ICH GCP and related regulations.
Consider building your career as a Global GCP Auditor | Data Integrity & CAPA at CSL Vifor.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global GCP Auditor | Data Integrity & CAPA role in the description above.
We appreciate your interest in this position.
Join CSL Vifor and contribute to our ongoing work.
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