193 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.

Senior Systems Engineer - Battery Systems manages systems engineering in battery development and test projects. Responsibilities include designing battery systems, integrating subsystems, and ensuring compliance with standards throughout the lifecycle. Requires 4-7 years in related engineering fields.

Electrical Systems Design Engineer responsible for electrical design of industrial plants, special systems, and machinery for engine and vehicle testing. Requires Electrical Engineering degree and 3+ years in industrial electrical system design.

Senior High Voltage E/E Engineer responsible for systems engineering of high voltage systems. Focus includes design, integration, verification, and validation of battery and HV systems, ensuring compliance with safety standards.

EFSA invites Guest Scientists and Professionals to join projects at the European Food Safety Authority. Open to candidates from public administration, universities, or IGOs with B2 English knowledge.

FP&A Business Partner for an industrial company. Support planning, forecasting, and performance management across European operations. Requires 4-6 years in Big Four/international manufacturing FP&A.

Accounting & Tax Manager for a multinational industrial company. Oversee accounting, tax, and administrative processes across Italy, France, and Spain. Manage financial closings, compliance, and Group reporting.

Supply Chain & Logistics Engineer to support continuous improvement of logistics processes across the manufacturing network. Responsibilities include optimizing material flows, leading packaging initiatives, and supporting transportation management. Requires a degree in a related field and 1-2 years of experience.

Lead Statistical Programmer responsible for SAS programming for clinical and safety data systems. Develop work-plans, ensure data integrity, and create CDISC-compliant deliverables for regulatory submission. Requires 7+ 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.

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 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.

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.

Bio-analytical Scientist develops and optimizes analytical methods for protein-based products. Requires 8+ years in chemical/biochemical lab work with protein products or 5 years with a PhD.

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.

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.

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.

GCP Specialist in R&D Auditing responsible for ensuring compliance and managing GCP CAPAs. Duties include executing first and second party audits, managing quality metrics, and finalizing audit reports. Requires 3+ years in Pharma/CRO QA with strong GCP knowledge.

Senior Technical Leader for Protein Biologics Development in GRD CMC. Lead CMC strategies for recombinant protein therapeutics, covering expression, upstream/downstream process development, and quality attributes.