194 English-speaking jobs in Emilia-Romagna

Order to Cash Team Leader manages end-to-end processes, overseeing Accounts Receivable, DSO, and collections. This role requires experience in O2C/AR, strong organizational skills, and knowledge of VAT and financial processes.

Lead Molding operations for a global medtech company, managing a large production organization. Ensure production targets, quality standards, and operational performance are met while driving continuous improvement.

Senior System Verification Engineer to lead system-level verification of integrated hardware and software medical devices. Define strategies, execute testing (functional, safety), and ensure compliance with international standards.

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.

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 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.

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.

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 Technical Leader, GRD CMC, manages CMC development and IMP supply strategy for rare disease projects. Requires 10+ years in pharma, expertise in drug substance/product development, and experience with EMA/FDA regulatory interactions.

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.

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 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.

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 Technical Leader in GRD CMC with end-to-end responsibility for CMC strategy, execution, and risk management. Expertise includes analytical method development, validation, and control strategy for biological products.

Manage QMS, inspections, and site compliance ensuring GMP adherence to FDA and EU regulations. Develop procedures, analyze quality data, and drive continuous improvement in pharmaceutical manufacturing.

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.

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.

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.

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.

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.