247 English-speaking jobs in Emilia-Romagna

Design, develop, and maintain software for diagnosing and monitoring complex systems using C/C++. Requires proficiency in C/C++, object-oriented design, and experience with Linux Embedded systems.

Electrical System Engineer designs ETO projects like Static Transfer Switches and Power Switches. Responsibilities include creating designs, drawings, and BOM, while meeting schedule, manufacturability, and cost goals.

Power Converter Engineer to assess new converter architectures and components. Analyze and test conversion topologies, verify performance via lab tests, and define product specs. Requires Electrical/Electronic Engineering degree and 3+ years in UPS or power conversion.

Provide thought leadership for Large Power UPS offerings, owning the full lifecycle from ideation to End of Life. Develop market direction, business cases, and sales enablement tools. Requires technical expertise and strong analytical skills.

Customer Engineer AC Power responsible for startups, maintenance, and emergency repairs of Vertiv UPS and power equipment. Requires technical service experience with AC Power, strong communication, and ability to work under pressure.

Lead EHS programs for large-scale construction and infrastructure projects. Oversee safety strategy, regulatory compliance, and risk mitigation. Requires 8-10 years of construction safety experience and relevant certifications.

Product Engineer for Energy Storage acts as design owner for large battery backup products using lithium-ion or other battery chemistry. Requires Electrical/Electronic Engineering degree and 2+ years of experience.

Design, analyze, and troubleshoot firmware code for embedded systems. This role involves hardware understanding, defining firmware tests, and producing technical documentation. Requires C language experience and knowledge of communication protocols.

Senior Firmware and Control Engineer to design, analyze, and troubleshoot embedded firmware code. Responsibilities include defining tests, technical documentation, and providing customer support. Requires C language skills and knowledge of DSP/MCU architecture.

Manage the lifecycle of server rack solutions, enclosures, and physical infrastructure. Define product roadmaps, analyze EMEA demand, and drive product launches. Requires 5+ years of experience in a comparable role.

Principal Regulatory Writer for Global Rare Diseases. Author, review, and manage regulatory documents for global health authorities, translating clinical and CMC data for drug submissions and lifecycle activities.

Develop data visualization to transform complex data into understandable formats. Responsibilities include data analysis, creating visual representations, and developing tools using Python or R. Requires a degree in Data Science or Computer Science.

This role supports Lifecycle Management & Launch Excellence by providing operational, analytical, and governance support. Responsibilities include driving execution, KPI reporting, and business analyses across priority markets.

Define and execute the global publication strategy and tactical plan for all global studies. Ensure timely, compliant dissemination of scientific data via congress presentations and peer-reviewed publications.

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

Manage the Pharmacovigilance System Master File (PSMF) and ensure compliance with regulatory requirements. Evaluate guidelines, update PSMF documentation, and contribute to PV KPI definition and reporting.

Maintenance Engineer responsible for equipment reliability and continuous improvement in a manufacturing environment. Duties include mechanical/electrical repairs, procedure development, and fault diagnosis. Requires 5+ years of experience, preferably in pharmaceuticals.

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.

Senior Director, Clinical Biometrics & Analytics, leads Data Management, Biostatistics, and Statistical Programming within Global Clinical Development. This role drives clinical data strategy, ensuring scientific rigor and regulatory compliance across drug development phases.

Support decision-making with data-driven insights and long-term projections for the R&D pipeline. Elaborate analyses on pipeline value, timelines, and resource demand. Manage standardized project cards and support R&D strategy definition.