189 English-speaking jobs in Emilia-Romagna

Lead Molding operations for a global medtech company, managing a large production organization. Ensure production targets, quality standards, and operational performance are met while driving continuous improvement.

Order to Cash Team Leader manages end-to-end processes, overseeing Accounts Receivable, DSO, and collections. This role requires experience in O2C/AR, strong organizational skills, and knowledge of VAT and financial processes.

SAP Controlling Business Analyst to optimize global financial and cost management processes. This role designs and configures SAP CO and PS modules, acting as a link between business and IT. Requires 3+ years in SAP CO/PS and fluency in English.

Datalogic seeks a Global R&D Director to lead mobile computing technology strategy and product development. This role owns the full product lifecycle, managing global teams and ODM partners. Requires 10+ years in R&D leadership with expertise in mobile computing and connected hardware.

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.

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 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.

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

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.

Manage QMS, inspections, and site compliance ensuring GMP adherence to FDA and EU regulations. Develop procedures, analyze quality data, and drive continuous improvement in pharmaceutical manufacturing.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.