192 English-speaking jobs in Emilia-Romagna

Senior GDP QA Specialist to strengthen the Good Distribution Practice Quality Management System. Responsibilities include managing deviations, change control, audits, and temperature excursions while ensuring regulatory compliance.

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.

Manage training and documentation across Global TechOps & Supply. Oversee EDMS and training systems, ensuring regulatory compliance. Requires 5+ years in pharma QA with knowledge of EU/FDA guidelines.

The Global New Product Planning Manager will complete strategic commercial assessments to drive early pipeline development and due diligence for the AIR franchise. This role involves assessing market landscapes, competitive dynamics, and developing investment stories.

This role ensures control and validation of software systems in GXP processes, managing computerized system validation. Responsibilities include drafting validation documentation and managing change control. Requires 5+ years in CSV within the pharmaceutical industry.

Clinical Partnership Manager to optimize governance and operations of strategic partnerships with CROs. Develop trust-based vendor relationships, manage performance, and ensure high-quality clinical trial delivery. Requires 8-10 years in Clinical Operations.

Support Chiesi's Global Workplace and Real Estate strategy across affiliates. This role manages workplace standards, office transformations, location evaluations, and real estate portfolio visibility. Requires a Master's degree and 3-6 years of relevant experience.

Bio-analytical Scientist develops and optimizes analytical methods for protein-based products. Requires 8+ years in chemical/biochemical lab work with protein products or 5 years with a PhD.

GCP Specialist in R&D Auditing responsible for ensuring compliance and managing GCP CAPAs. Duties include executing first and second party audits, managing quality metrics, and finalizing audit reports. Requires 3+ years in Pharma/CRO QA with strong GCP knowledge.

Senior Manager, CMC Regulatory Affairs, Global Rare Diseases. Direct experience in post-approval CMC activities to support the GRD portfolio worldwide. Responsible for authoring/reviewing CMC sections for global submissions.

Senior Manager to shape R&D digital transformation by designing data-driven processes using platforms like Veeva Vault. This role orchestrates process excellence, digital innovation, and change management across the drug development lifecycle.

Lead Statistical Programmer responsible for SAS programming for clinical and safety data systems. Develop work-plans, ensure data integrity, and create CDISC-compliant deliverables for regulatory submission. Requires 7+ years of experience.

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.

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.

This role designs application solutions by analyzing user needs, defining functional requirements, and mapping business processes. The specialist monitors development, participates in testing, and coordinates with ICT functions for successful implementation.

The Real Estate & Facility Coordinator ensures building systems operate across the lifecycle. This role involves first-level technical troubleshooting, managing maintenance, and overseeing infrastructure at various Italian branches.

The Export Area Supervisor implements brand distribution activities and contributes to sales objectives. Responsibilities include supporting sales development, supervising the distribution network, leading the sales team, and managing customer portfolios.

Senior R&D Industrial Controller to act as finance business partner for R&D projects. Responsibilities include monitoring costs, supporting budgeting, and managing R&D cost reporting. Requires a business degree and 5+ years in controlling.

Manage domestic and international shipments, coordinating logistics, customs documentation, and liaising with freight forwarders. Requires 5+ years in Import/Export, knowledge of transport modes, and SAP experience.

Buyer for Mechanical Custom Parts to manage procurement for custom-designed components. Responsibilities include supplier selection, negotiations, and purchase order management. Requires 5-7 years in purchasing mechanical components.