17 set - Bardi
Kühne + Nagel
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 ******** 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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