216 English-speaking jobs in Emilia-Romagna

Junior Analyst supporting consulting projects in Wealth Management. Tasks include functional analysis, financial model development, and drafting evaluation reports. Requires a post-graduate degree in Math, Physics, Finance, or Financial Engineering and proficiency in Python.

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.

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.

Manage GCP compliance, CAPAs, and quality metrics within Global R&D. Execute first and second-party audits and finalize quality documents. Requires 3+ years in Pharma/CRO QA with strong GCP knowledge.

Develop, optimize, and execute analytical methods for protein-based products. Requires 8+ years in chemical/biochemical lab work with protein products or 5 years with a PhD. Knowledge of various analytical techniques is essential.

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.

Ensure pharmacovigilance quality system compliance with regulations and standards. Manage deviations, monitor CAPAs, and review SOP/WIs. Requires Life Sciences degree and 3-5 years in pharmacovigilance/QA.

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.

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.

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 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.

Senior Manager, CMC Regulatory Affairs, Global Rare Diseases. Requires 7+ years of Regulatory CMC experience, 3+ in Biologics/Biopharmaceuticals, and advanced knowledge of global CMC regulations.

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

Senior Technical Leader in GRD CMC with end-to-end responsibility for CMC strategy, execution, and risk management. Expertise includes analytical method development, validation, and control strategy for biological products.

Manage training and documentation across Global TechOps & Supply. Oversee EDMS, training systems, and document control, ensuring regulatory compliance. Requires 5+ years in pharma QA with scientific degree.

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.

Senior GDP QA Specialist to strengthen the Good Distribution Practice Quality Management System. Responsibilities include managing deviations, change control, complaints, and risk assessments to ensure regulatory compliance.

Manage pharmacovigilance operations for interventional clinical trials, ensuring compliance with PV legislation. Support safety data collection, process maintenance, and CRO oversight within R&D. Requires a Master's degree and 3+ years in Pharmacovigilance or Clinical Research.

Senior Technical Leader for Protein Biologics Development in GRD CMC. Lead CMC strategies for recombinant protein therapeutics, covering expression, upstream/downstream process development, and quality attributes.