194 English-speaking jobs in Emilia-Romagna

SAP FI-CO Application Specialist to support IT strategy alignment with business strategy in Finance, Controlling, and Industrial areas. Requires 5+ years in IT support with deep SAP FI/CO knowledge and S/4HANA experience.

Mechanical Operations Quality Specialist to lead problem-solving for manufacturing issues and ensure quality standards. Responsibilities include audits, root cause analysis, and continuous improvement using structured methodologies. Requires 3+ years in quality control and an Engineering degree.

Manufacturing Technology Specialist needed for process engineering. Define production equipment, validate concepts, and implement manufacturing processes for new product development. Requires Mechanical/Automation Engineering background and Lean Manufacturing knowledge.

Commercial Sales Controller supports HQ Finance by steering business operations. Responsibilities include sales reporting, managing commercial performance forecasts, and preparing P&L variance analyses. Requires a Master's degree and 6-8 years of relevant experience.

Detail-oriented Buyer Far East to manage supplier relationships and negotiate contracts for materials from Taiwan, South Korea, or other Eastern suppliers. Develop sourcing strategies and secure favorable terms.

Brand Communication Manager to define and promote brand image and identity. Develop cohesive communication strategies across channels, manage brand assets, and support sales and institutional activities. Requires 5+ years in Brand Identity roles.

Principal Regulatory Writer for Global Rare Diseases. Author, review, and manage regulatory documents for global health authorities, translating clinical and CMC data for drug submissions and lifecycle activities.

Manage the Pharmacovigilance System Master File (PSMF) and ensure compliance with regulatory requirements. Evaluate guidelines, update PSMF documentation, and contribute to PV KPI definition and reporting.

Lead global post-marketing pharmacovigilance operations, ensuring data quality and compliance across Chiesi's portfolio. Oversee safety data collection, literature review, and regulatory adherence.

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.

Define and execute the global publication strategy and tactical plan for all global studies. Ensure timely, compliant dissemination of scientific data via congress presentations and peer-reviewed publications.

This role ensures control and validation of software systems in GXP processes. Responsibilities include drafting validation plans, managing changes, and acting as a Technical Expert in audits. Requires 5+ years in CSV in the pharmaceutical industry.

Maintenance Engineer responsible for equipment reliability and continuous improvement in a manufacturing environment. Duties include mechanical/electrical repairs, procedure development, and fault diagnosis. Requires 5+ years of experience, preferably in pharmaceuticals.

The Patient Safety Science Lead provides safety-scientific expertise for safety science activities and clinical development. This role manages safety surveillance and risk management, ensuring proactive, science-driven safety evaluation.

Develop data visualization to transform complex data into understandable formats. Responsibilities include data analysis, creating visual representations, and developing tools using Python or R. Requires a degree in Data Science or Computer Science.

Senior Director, Clinical Biometrics & Analytics, leads Data Management, Biostatistics, and Statistical Programming within Global Clinical Development. This role drives clinical data strategy, ensuring scientific rigor and regulatory compliance across drug development phases.

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.

Support decision-making with data-driven insights and long-term projections for the R&D pipeline. Elaborate analyses on pipeline value, timelines, and resource demand. Manage standardized project cards and support R&D strategy definition.

Provide legal support to Staff and Global R&D functions, including contract drafting, negotiation, and risk evaluation. Requires a Master's in law and 2-3 years of experience in pharma or a top law firm.

This role supports Lifecycle Management & Launch Excellence by providing operational, analytical, and governance support. Responsibilities include driving execution, KPI reporting, and business analyses across priority markets.