This is a senior site-based
quality role with responsibility for managing and developing the
Quality Management System to ensure full GxP compliance. As
QA Systems
Manager, you’ll act as a key member of the
Quality leadership team and take ownership of site-wide
quality processes … as site lead for data integrity, ensuring systems and processes support secure, traceable and compliant data management Oversee the validation master plan and provide
QA oversight for validation-related activities across the site Manage and improve key
quality systems including change control, CAPA, deviations, document control and training compliance … readiness and internal performance monitoring Contribute to
Quality leadership team projects and initiatives to enhance overall site compliance Ideal Experience: Extensive experience in pharmaceutical
QA, with a strong understanding of GMP and GDP Proven track record in managing QMS elements, including validation, documentation, and data integrity Experience supporting inspections
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