193 English-speaking jobs in Emilia-Romagna

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.

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

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.

Senior Technical Leader, GRD CMC, manages CMC development and IMP supply strategy for rare disease projects. Requires 10+ years in pharma, expertise in drug substance/product development, and experience with EMA/FDA regulatory interactions.

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.

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.

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

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.

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.

Senior Clinical Project Manager coordinates operational management of clinical trials to develop compounds. Responsibilities include managing CROs, budget adherence, and ensuring compliance with SOP and GCP standards. Requires 3+ years of experience.

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.

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, preferably in pharma.

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.

Senior Analytical Scientist needed for LNP/RNA analytics. Drive analytical development and control strategy for gene editing products, including mRNA-LNP modalities. Expertise in UPLC, DLS, LC-MS, and NGS is required.

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 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.

Senior Director, R&D Portfolio and Program Management, provides strategic leadership for the Cardiopulmonary R&D pipeline. This role leads the CP R&D Portfolio Management operating model, managing project heads and PMO across global development programs.

Senior System Verification Engineer to lead system-level verification of integrated hardware and software medical devices. Define strategies, execute testing (functional, safety), and ensure compliance with international standards.

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.