Overview In this role you will ensure regulatory compliance and quality excellence within a pharmaceutical logistics context. You work closely with a technical quality team to maintain GXP-compliant systems, manage permits, and support regulatory submissions. You will drive CAPA execution, update procedures, and contribute to process innovation. This position offers a stable environment with growth opportunities and international exposure.
Retribuzione / Benefits safe and stable environment focus on physical and mental well-being professional growth opportunities international opportunities Responsabilità Ensure import/export permits align with customer requests and timely regulatory notifications to health authorities Maintain and implement a compliant quality management system per site authorizations and product-specific requirements Approve and manage CAPA plan execution Ensure temperature monitoring of warehouse and critical systems remains GXP-compliant Update and approve procedures and operating instructions to support all processes Participate in process reviews to push for quality process innovation Support regulatory documentation preparation for AIFA and other bodies Requisiti fondamentali ~ Qualified Person (Dlgs 219/2006 and amendments) ~ Responsible Person at pharmaceutical site ~ Master in Biology ~5+ years in similar roles ~ Excellent use of Excel and data analysis ~ Advanced English ~ Driving license and own car ~ Time flexibility during induction ~ Excel and data analysis ~ GXP/compliance ~ Quality management systems ~ CAPA ~ Regulatory documentation preparation ~ AIFA/regulatory submissions
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