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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