We are seeking an experienced IT Operations Engineer to oversee IT infrastructure and operational activities within a GxP-regulated pharmaceutical environment. This is a hands‐on, high‐visibility role requiring strong operational leadership, stakeholder management, and compliance experience within regulated pharma environments. Qualsiasi informazione aggiuntiva su questo lavoro è disponibile nel testo sottostante. Si assicuri di leggere attentamente, quindi invii la sua candidatura. Location: L'Aquila, Italy Role Type: Long-term engagement Working schedule: 5 days/week during standard business hours (Out-of-hours availability required for urgent P1/P2 incidents) Language Requirements: Fluent Italian and English (written and spoken) Key Responsibilities Operational Leadership Serve as the primary on‐site IT operations lead for the pharmaceutical site Coordinate daily operational activities across infrastructure, systems, laboratories, and industrial IT environments Act as the escalation point for operational and service‐related issues Ensure effective communication between IT, QA, Facilities, Engineering, Manufacturing, and R&D stakeholders Change & Release Management Oversee change management processes for GxP-regulated systems Participate in Change Advisory Board (CAB) activities Ensure all changes follow approved validation, testing, and documentation procedures Coordinate implementation windows and operational readiness activities Incident & Service Management Manage operational incidents including P1/P2 critical events Coordinate troubleshooting, escalation, vendor engagement, and resolution activities Ensure adherence to SLA and operational response targets Provide out-of-hours support coverage as required Compliance & Quality Maintain compliance with pharmaceutical and regulatory requirements Support audit readiness and regulatory inspections Ensure proper maintenance of GxP asset inventories and configuration records Support validation lifecycle activities and documentation reviews Operate within established Quality Management System (QMS) procedures Asset & Infrastructure Oversight Maintain oversight of IT‐managed laboratory and industrial equipment Ensure asset lifecycle tracking, configuration management, and validation status reporting Coordinate patching and maintenance activities under strict approval and testing controls Support infrastructure continuity, operational resilience, and service stability The role requires prior experience working within regulated pharmaceutical or life sciences environments, including familiarity with: EU GMP FDA 21 CFR Part 11 GAMP 5 Quality Management Systems (QMS) Computer System Validation (CSV) concepts Regulated change control and documentation standards Requirements The ideal candidate will demonstrate: xrdztoy Proven experience in pharmaceutical or GxP-regulated IT environments Strong background in site-level IT operations, infrastructure management, or service delivery leadership Experience supporting regulatory audits and inspections Strong stakeholder engagement and communication skills Ability to coordinate across technical, operational, and quality teams Experience managing critical incidents and operational escalations Strong understanding of operational governance and compliance processes Full‐time on‐site presence during business hours (5 days/week) Availability for P1/P2 incidents outside standard hours Reachable within 30 minutes for critical operational escalations Participation in planned maintenance, audits, and major operational activities outside standard hours, where required Support critical incident coverage Ensure uninterrupted service availability #J-18808-Ljbffr