628 English-speaking jobs in Emilia-Romagna

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.

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.

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 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.

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 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.

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.

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.

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.

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.

At PwC, our people in audit and assurance focus on providing independent and objective assessments of financial statements, internal controls, and other assurable information enhancing the credibility and reliability of this information with a variety of stakeholders. They evaluate compliance with regulations including assessing governance and risk management processes and related controls.

Procurement Specialist needed for maternity leave replacement. Manage purchasing activities for raw materials, components, and parts, ensuring cost-effectiveness, quality, and timely delivery. Collaborate with suppliers and internal stakeholders to optimize purchasing processes.

Develop and expand ARAG's presence in international markets, focusing on Europe. Identify and pursue new business opportunities, build relationships with OEM customers and distribution networks, and drive market penetration.

Communication Officer to support content development and promotion for the EFSA 2027 conference. Responsibilities include drafting and publishing website updates, social media promotion, and preparing responses for media inquiries. Requires excellent English (C1 level), experience in scientific and institutional content creation, social media management, and EU institutional communication.

Senior Director, Clinical Biometrics & Analytics will lead Data Management, Biostatistics, and Statistical Programming functions. This role defines and executes data and statistical strategies across all phases of drug development, ensuring scientific rigor, operational efficiency, and regulatory compliance.

PwC seeks a Junior Financial Services Auditor to provide independent assessments of financial statements, internal controls, and other assurable information. The role requires a learning mindset, strong communication skills, and the ability to apply professional and technical standards.

Intern will support the FP&A team in tasks such as monthly reporting, budget forecasting, and business performance analysis. The intern will collaborate with various departments and affiliates within Chiesi Group.

Intern to support the planning, development, and execution of internal communications strategies and initiatives. Responsibilities include managing communication channels, supporting corporate events, and collaborating with stakeholders.

Manages the implementation and optimization of technologies for first-party data collection, enrichment, and activation in paid media and direct marketing. Leads cross-functional collaboration between digital, media, data, legal, and IT teams. Supports operational activities for omnichannel marketing automation, reporting, and data projects. Collaborates with stakeholders to improve first-party data collection technologies and ensure compliance with privacy regulations. Provides day-to-day support for technical activities related to consumer promotions and coordinates with agencies and vendors.