594 English-speaking jobs in Emilia-Romagna

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.

Mechanical Engineer to design and develop advanced mechanical and mechatronics systems for precision agriculture equipment. Minimum 5 years experience, Master's degree in Mechanical Engineering, and strong CAD and PLM skills required.

The Global Commercial Analytics & Customer Insights Manager generates, collects, and analyzes business, customer, and commercial data to drive strategic value. This role acts as the global source of truth for commercial data, enabling data-driven decisions across Chiesi brands and markets. Responsibilities include developing analytics solutions, leading customer insights projects, and supporting strategic decision-making. The ideal candidate has 5-7+ years of experience in commercial analytics, customer insights, or BI within global healthcare organizations.

The R&D Patient Engagement & Projects Intern will support the R&D Patient Engagement team in maintaining and increasing awareness of Patient Engagement impact throughout Chiesi AIR, RARE and CARE franchise projects. The intern will support the implementation of digital campaigns, identify and contribute to global initiatives for promoting innovation in clinical research, and act as the main point of contact between R&D Patient Engagement and internal functions.

Intern to support planning, developing, and executing internal communications strategies and initiatives. Responsibilities include managing communication channels, supporting corporate events, and collaborating with stakeholders.

Intern will support competitor and target analyses and contribute to research projects across Chiesi's therapeutic areas. Responsibilities include monitoring scientific information, conducting bibliographic research, and supporting strategic exercises.

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

Develops a range of pharmacovigilance documents for global products, including Periodic Safety Reports and Safety Strategy Documents. Supports the Coordinator in global planning and monitors compliance for submitted reports.

The Real World Evidence Lead will shape and execute the organization's RWE vision, building and improving RWE capabilities, establishing robust processes, and driving impactful evidence generation. Responsibilities include leading the development and implementation of RWE strategies, overseeing RWE studies conducted through CROs, and providing strategic oversight for study design, initiation, and execution. The ideal candidate will have an advanced degree in epidemiology, public health, health economics, or a related field, significant experience in RWE, observational research, or related disciplines, and proven ability to lead and execute RWE projects.

The Operational Excellence Manager leads and implements initiatives to drive continuous improvement, enhance operational efficiency, and ensure high-quality standards across pharmaceutical manufacturing processes.

The IT Application Manager & Functional Business Analyst partners with Track & Trace and HSE teams to translate business needs into IT solutions. Responsibilities include functional analysis, application ownership, and solution evolution within a regulated pharmaceutical environment. The role requires 5+ years of IT experience, preferably as a Functional Analyst and/or Application Manager, with solid knowledge of Manufacturing processes and experience working in regulated environments (GxP).

The Quality & Compliance System Senior Specialist manages inspections, training, documentation, site compliance, quality KPIs, and master document preparation. This role ensures GMP compliance with standards, regulations, and guidelines. Responsibilities include developing and implementing QMS, monitoring quality data, preparing reports, collaborating with cross-functional teams, investigating quality issues, and promoting continuous improvement.

Manages and coordinates the life cycle management of external platforms, ensuring production outputs align with annual requirements. Optimizes and validates injection molding and assembly processes, acting as technical authority in these areas. Leads capital projects related to equipment installation or refurbishment. Supports validation activities and manages tool and assembly line refurbishment. Drives operational engineering evolution programs and monitors maintenance KPIs. Requires a degree in Mechanical Engineering and at least 5 years of experience in an engineering environment. Fluent English is required.

Senior clinical development leader responsible for shaping and executing global clinical development strategy for Bronchiectasis, Pulmonary Hypertension, and Interstitial Lung Diseases. Leads a team of Clinical Development professionals and oversees clinical trial design, execution, and regulatory submissions. Requires 8-10 years of experience in pharmaceutical R&D with a track record of driving programs from early development through approval. MD required, board certification in pulmonology preferred. Fluency in English required.

The Global Medical Information Specialist Intern will support the Global Medical Information function in providing accurate and scientifically sound medical information. The intern will assist with preparing responses to medical inquiries, conducting literature searches, and drafting medical information materials.

Supports the full Organic Campaign cycle, collaborating with clients to deliver digital advertising campaigns. Assists with campaign implementation, monitoring progress, and optimization. Provides support to the Sales Team in identifying campaign targets.

Full Stack Developer needed for a multinational group in the industrial sector. Responsibilities include product requirements analysis, software development, maintenance, and validation for embedded systems and SCADA systems.

Technogym seeks an Electronic Supplier Quality Engineer to manage, monitor, and improve supply chain performance. Responsibilities include coordinating supplier development, managing quality documentation, and promoting corrective actions. The ideal candidate has a Master's Degree in Engineering (preferably Electronic), 3-5 years of relevant experience, and knowledge of APQP, PPAP, and 6sigma methodologies.

Senior HR Reward will develop and manage competitive compensation and benefits programs. Requires 5+ years of experience in a similar role, HR ERP system knowledge, and strong analytical and relational skills.