CSV/QAV Validation Consultants (Multiple Roles)
Are you an experienced professional in Computer System Validation (CSV) or Quality Assurance Validation (QAV)? We’re hiring across multiple projects, including opportunities within Ireland and a major organization in France.
Key Responsibilities
Lead or support CSV activities, ensuring GAMP5, 21 CFR Part 11, and Annex 11 compliance.
Develop and execute validation protocols (IQ/OQ/PQ) for IT systems, equipment, or processes.
Oversee risk management, CAPA, and deviation management within GxP environments.
Ensure audit readiness and contribute to continuous improvement in regulated environments.
We’re looking for
Professionals with experience in CSV, QAV, or validation engineering.
Familiarity with FDA QMSR, ISO standards, and GxP systems.
A proactive approach to quality, problem-solving, and collaborative work.
Location: Various (including Ireland, South of France, and remote options).
Ready to bring your validation expertise to dynamic projects? Apply today or reach out for more info!
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