188 English-speaking jobs in Emilia-Romagna

Manage ETCS/System functional testing by defining V&V strategy, planning tests, and executing SW/data analysis. Requires an Engineering degree in relevant fields and willingness to perform weekly on-field activities.

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.

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.

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.

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.

Design and deliver advanced TMS and ATS subsystems, ensuring seamless system integration. Responsibilities include system detailed design, supporting Testing & Commissioning, and managing work packages.

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.

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.

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.

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.

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.

Senior GDP QA Specialist to strengthen the Good Distribution Practice Quality Management System. Responsibilities include managing deviations, change control, audits, and temperature excursions while ensuring regulatory compliance.

Senior Analytical Scientist needed for LNP/RNA analytics. Drive analytical development and control strategy for gene editing products, including mRNA-LNP modalities. Expertise in UPLC, DLS, LC-MS, and NGS is required.

Senior Process Scientist needed for gRNA process development. Lead process development and manufacturing oversight for gene therapy programs, specializing in synthetic nucleotide and gRNA development. Requires 5-10 years in biotech with expertise in gene editing and GMP.

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.

Drive global supplier quality oversight and lifecycle management for APIs, packaging, and critical GxP suppliers. Define strategy, governance, and performance monitoring across the supply chain.

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.

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

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.

This role ensures control and validation of software systems in GXP processes, managing computerized system validation. Responsibilities include drafting validation documentation and managing change control. Requires 5+ years in CSV within the pharmaceutical industry.