212 English-speaking jobs in Emilia-Romagna

Design, build, and operationalize data processing systems in a cloud-native environment. This Azure Data Architect role transforms raw data into business value, supporting Big Data projects. Requires experience with Azure, Big Data architectures, and relevant programming.

Databricks Expert needed to bridge Data Science and Data Engineering. Support Big Data projects, delivering data acquisition, transformation, and loading into data lakes. Requires cloud experience (GCP/AWS/Azure) and skills in Spark, Python, and SQL.

Data Architect/Engineer role to design, build, and operationalize data processing systems on GCP. Requires 5-10 years in data engineering, expertise in Scala/Java/Python, and knowledge of GCP services like BigQuery and Dataflow.

Master Data Architect AWS role managing AWS Center of Excellence and leading Data & Analytics projects. Requires 5+ years managing BI/data analysts and experience designing data platforms on AWS.

AWS Data Architect supporting customer AWS Data Platform projects. Design and optimize data pipeline architecture using AWS services like GLUE, Lambda, Redshift, and S3. Requires 5+ years of AWS experience.

AWS Data Engineer role focusing on AWS Data Platform projects. Responsibilities include data acquisition, transformation, and loading into data lakes. Requires experience in cloud environments, Big Data Architectures, and proficiency in Java, Python, or Scala.

Support Big Data projects by delivering data acquisition, transformation, and loading into data lakes. Requires experience in cloud native environments, Big Data Architectures, and tools like Azure Data Factory and Spark.

Senior Data Scientist specializing in GenAI solutions. Requires 3-5 years of experience, strong Python and SQL, and expertise in ML/Deep Learning, including TensorFlow/PyTorch. Focus on full-stack project execution.

Senior Manager to drive R&D digital transformation by designing and implementing data-driven processes using platforms like Veeva Vault. This role orchestrates process excellence, digital innovation, and change management across functions.

Lead Scientist role driving upstream bioprocess industrialization and lifecycle management. Responsibilities include process insourcing, technology transfer, scale-up, and validation, ensuring robust, compliant manufacturing. Requires MSc/PhD and 10+ years in biologics CMC.

Manage the Pharmacovigilance System Master File (PSMF) and ensure compliance with regulatory requirements. Evaluate guidelines, update PSMF documentation, define KPIs, and report on PV system performance. Requires a Master's degree and 5+ years in international Pharmacovigilance.

Provide legal support to Staff and Global R&D functions, including contract drafting, negotiation, and risk evaluation. Responsibilities cover finance, procurement, sustainability, and clinical/preclinical studies. Requires a Master's in law and 2-3 years of relevant experience.

Senior Clinical Project Manager coordinates operational management for assigned projects to develop compounds. Responsibilities include managing clinical trials, CRO oversight, budget adherence, and ensuring compliance with SOP and GCP.

Clinical Partnership Manager to optimize governance and operational models for strategic CRO partnerships. Develop and manage vendor relationships, ensuring high-quality clinical trial delivery and continuous improvement. Requires 8-10 years in Clinical Operations.

Senior Process Scientist needed for gRNA process development. Lead process development and manufacturing oversight for gene therapy programs, focusing on in vivo LNP programs. Expertise in gRNA development, synthetic nucleotide manufacturing, and CRO/CDMO management is required.

Financial Controller supporting the Core Markets Business Unit. Responsibilities include month-end/year-end close, financial reporting, planning, and performance monitoring across international markets. Requires 4+ years in international finance.

The Global New Product Planning Manager will complete strategic commercial assessments to drive early pipeline development and due diligence. Responsibilities include assessing market landscapes, revenue forecasts, and developing investment stories. A medical or scientific background is preferred.

Principal Regulatory Writer for Global Rare Diseases. Author, review, and manage regulatory documents for global health authorities, translating clinical and CMC data into compliant submissions across the product lifecycle.

Senior Analytical Scientist specializing in LNP/RNA analytics. Drive analytical development and control strategy for gene editing products, including mRNA-LNP characterization using UPLC/UHPLC, DLS, and LC-MS. Manage CRO/CDMO activities.

Lead global post-marketing pharmacovigilance operations, ensuring data quality and compliance for Chiesi's portfolio. Oversee safety data collection, literature review, and stakeholder engagement.