194 English-speaking jobs in Emilia-Romagna

  • Technogym
  • Diegaro
  • August 10
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.
  • Technogym
  • Diegaro
  • August 10
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.
  • Technogym
  • Diegaro
  • August 10
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.
  • Technogym
  • Diegaro
  • August 10
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.
  • Technogym
  • Diegaro
  • August 10
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.
  • Technogym
  • Diegaro
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
Lead global post-marketing pharmacovigilance operations, ensuring data quality and compliance across Chiesi's portfolio. Oversee safety data collection, literature review, and regulatory adherence.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
  • Chiesi
  • Parma
  • August 10
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.
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