189 English-speaking jobs in Emilia-Romagna

Project Engineering Manager accountable for TMS Engineering QCD and performance from requirement analysis to customer acceptance. Requires engineering degree, full lifecycle project deployment experience, and strong technical/leadership skills.

The Project Contract Manager guides contract and claim management and risk mitigation strategies. This role involves ensuring compliance with CCIM, monitoring contractual obligations, and managing claims documentation. Travel up to 30% is required.

Execute test and commissioning activities on field for railway signalling systems supporting projects. Responsibilities include testing, defect identification, tool calibration, and ensuring compliance with safety and quality standards.

IXL Project V&V Designer tests IXL functionalities, defining and executing lab and on-site tests using standard V&V methods. Requires an Engineering degree in relevant fields and strong teamwork.

Responsible for the full lifecycle of Traffic Management System software, including design, development, IT architecture, V&V, and support. Requires 20+ years in ICT, managing large international teams and complex software projects.

Service Signalling Maintenance Engineering Engineer to support lifecycle management and maintainability of railway signalling solutions. Requires an Engineering degree and strong interest in railway signalling systems.

Product Development Manager to organize program development, apply standards, and lead activities to deliver program items according to QCD commitments. This role involves managing technical risks and coordinating cross-functional teams.

This role designs application solutions by analyzing user needs, defining functional requirements, and mapping business processes. The specialist monitors development, participates in testing, and coordinates with ICT functions for successful implementation.

The Real Estate & Facility Coordinator ensures building systems operate across the lifecycle. This role involves first-level technical troubleshooting, managing maintenance, and overseeing infrastructure at various Italian branches.

The Export Area Supervisor implements brand distribution activities and contributes to sales objectives. Responsibilities include supporting sales development, supervising the distribution network, leading the sales team, and managing customer portfolios.

EFSA seeks Seconded National Experts from public administrations. Roles involve supporting scientific panels, data collection, and risk assessment. Candidates need 3+ years of relevant experience and English proficiency.

Senior Manager to shape R&D digital transformation by designing data-driven processes using platforms like Veeva Vault. This role orchestrates process excellence, digital innovation, and change management across the drug development lifecycle.

Clinical Partnership Manager to optimize governance and operations of strategic partnerships with CROs. Develop trust-based vendor relationships, manage performance, and ensure high-quality clinical trial delivery. Requires 8-10 years in Clinical Operations.

Lead global post-marketing pharmacovigilance operations, ensuring data quality, compliance, and integrity across the portfolio. Oversee safety data collection, literature review, and regulatory adherence.

The Global New Product Planning Manager will complete strategic commercial assessments to drive early pipeline development and due diligence for the AIR franchise. This role involves assessing market landscapes, competitive dynamics, and developing investment stories.

Support Chiesi's Global Workplace and Real Estate strategy across affiliates. This role manages workplace standards, office transformations, location evaluations, and real estate portfolio visibility. Requires a Master's degree and 3-6 years of relevant experience.

Senior Manager, CMC Regulatory Affairs, Global Rare Diseases. Direct experience in post-approval CMC activities to support the GRD portfolio worldwide. Responsible for authoring/reviewing CMC sections for global submissions.

Senior Clinical Project Manager coordinates operational management of clinical trials to develop compounds. Responsibilities include managing CROs, budget adherence, and ensuring compliance with SOP and GCP standards. Requires 3+ years of experience.

Principal Statistician for Global Rare Diseases. Provide statistical expertise for drug development programs, clinical trials, and regulatory submissions. Requires PhD/MSc in Statistics and 10+ years in clinical trials.

Manage training and documentation across Global TechOps & Supply. Oversee EDMS and training systems, ensuring regulatory compliance. Requires 5+ years in pharma QA with knowledge of EU/FDA guidelines.