579 English-speaking jobs in Emilia-Romagna

About the Company G. D is a leading organization headquartered in Bologna, Italy. As a key player in the high‑tech machineries production, we specialize in cutting‑edge technologies, shaping the future of industrial automation. Our business portfolio encompasses a wide range of innovative making and packing solutions, in particular for Modern Oral and Next Generation products.

About the Company ACMA is a leading organization headquartered in Bologna, Italy. As a key player in the consumer goods industry for over 100 years, we specialize in manufacturing packaging machines for a range of sectors, including Food, Personal Care, Home Care, Chemicals and E-Commerce.

The Senior Director, Global Quality Integration & Alliances defines, leads, and executes global quality integration activities for mergers, acquisitions, divestments, and growth initiatives. This role ensures acquired or partnered entities are integrated into the global Quality Management System (QMS) in a compliant, risk-based, and business-enabling manner. The position also provides global oversight of quality governance for external partners and alliances.

Process Engineer to manage and optimize pharmaceutical manufacturing processes, ensuring compliance with GMP and regulatory standards. Responsibilities include process validation, technology transfer, process improvement, and collaboration with cross-functional teams. Requires a Bachelor's or Master's degree in a relevant field and 8+ years of experience in pharmaceutical manufacturing or process engineering.

The Global Commercial Effectiveness Manager ensures a robust, data-driven customer engagement strategy built on the omnichannel go-to-market model. Responsibilities include leading global coordination of affiliates in the definition and execution of the Customer Engagement Impact Plan, defining the optimal channel mix, and driving definition of AS-IS and TO-BE omnichannel models. The role also involves defining and maintaining application success, customer success, and engagement effectiveness metrics, acting as the global data owner for Customer Engagement data, and collaborating with Global Marketing, Medical, Commercial Operations, Digital, IT, and Data teams.

Develops a range of pharmacovigilance documents for global products, including Periodic Safety Reports, Safety Strategy and Core Benefit-Risk Documents. Responsible for writing, consolidating, updating, and distributing aggregates for global products. Supports the Coordinator in global planning for both molecules under development and those with a Marketing Authorisation.

Subject Matter Expert for Process Validation and technical maintenance activities, supporting industrialization, product technology transfer and life cycle management for Respiratory, Orals & Small Molecules products. Provide specialist technical support to R&D, Operations, Quality and external stakeholders.

The Global Engineering Compliance & Risk Management Lead defines and maintains global engineering and maintenance compliance standards, ensuring alignment with regulatory requirements and industry best practices. The role provides technical leadership across all manufacturing sites, drives continuous improvement initiatives, and leads risk mitigation strategies.

The Training & Documentation Coordinator manages training and documentation for Global TechOps & Supply. Responsibilities include analyzing training needs, organizing courses, managing the documentation system, and supporting projects. Requires a degree in scientific subjects and at least 5 years of experience in pharmaceutical manufacturing.

The Real World Evidence Lead will shape and execute the organization's RWE vision, building and improving RWE capabilities and driving impactful evidence generation. Responsibilities include leading the development and implementation of RWE strategies, establishing processes, and overseeing studies conducted through CROs. The ideal candidate will have an advanced degree in a relevant field, significant experience in RWE, and proven ability to lead and execute RWE projects.

The Global Health Execution Intern will support the implementation and operational execution of Chiesi's Global Health strategy. The role supports cross-functional activities to enable sustainable and inclusive access to essential medicine in low-income countries.

Carries out GMP/ISO audits of GMD contractors, drafts quality agreements, and ensures supplier qualification and validation. Ensures the quality of global suppliers and monitors their performance. Collaborates in internal/external audit activities, participates in investigations into non-conformities, and evaluates change control in relation to suppliers. Conducts component supplier validation and qualitatively evaluates contractors. Requires a degree in scientific disciplines and 5 years of experience in auditing activities of sterile, biological medicinal products. Knowledge of national and international pharmaceutical legislation is necessary. Expertise in pharmaceutical products, sterile products manufacturing and control, biotechnology products, and auditing practices is required.

Global R&D QA Senior PV Auditor will manage PV audits of Chiesi Pharmacovigilance System, including planning, execution, and monitoring CAPA implementation. Responsibilities include contributing to the global PV audit strategy, reviewing PV SOPs, and providing expert inputs in projects. Requires at least 5+ years experience as a Pharmacovigilance Auditor or in Global PV System management and/or Quality Management System compliance.

The Global IBP Manager supports the execution and continuous improvement of the global Sales & Operations Planning process. The role prepares, structures, and facilitates the S&OP cycle, ensuring transparency and alignment between Demand, Supply, and Finance. The Global IBP Manager supports cross-functional alignment and contributes to the development and stabilization of the S&OP process.

This role drives the end-to-end planning and performance of assigned rare disease brands, balancing revenue delivery with patient supply continuity. The Global Junior Brand Planner will translate demand signals into supply plans, ensuring uninterrupted patient access and supporting revenue realization.

IT Finance and Administration Manager collaborates with business stakeholders to define IT strategy, identify requirements, and facilitate adoption of global solutions. Optimizes end-to-end Record to Report processes, particularly General Ledger Closing and Inventory valuation within SAP and Microsoft Power BI.

This 6-month internship supports R&D activities focused on shelf-stable pasta-based meal solutions. The intern will collect, organize, and analyze market and technical data, contribute to product development, and participate in testing new concepts.

Intern - Scientific Knowledge supports the development and implementation of Therapeutic Area Strategies. Responsibilities include assisting with competitor and target analyses, contributing to ad hoc research projects, and supporting Scientific Intelligence activities.

Develops a range of pharmacovigilance documents for global products, including Periodic Safety Reports, Safety Strategy and Core Benefit-Risk Documents. Responsible for writing, consolidating, updating, and distributing aggregates for global products. Supports the Coordinator in global planning for both molecules under development and those with a Marketing Authorisation. Minimum 1 year of experience in pharmacovigilance with practical knowledge of drafting PSUR/PBRER, PADER, ACO, RMP and DSURs. Master's degree in science, PhD or similar. Fluent in English.

Subject Matter Expert for Process Validation and technical maintenance activities, supporting industrialization, product technology transfer and life cycle management for Respiratory, Orals & Small Molecules products. Provide specialist technical support to R&D, Operations, Quality and external stakeholders.