191 English-speaking jobs in Emilia-Romagna

Spare Parts Sales Specialist supports spare part supply, managing inventory and coordinating with customers and internal teams. Requires an Engineering degree or Technical Diploma, experience in spare parts management, and B2 English proficiency.

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.

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.

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 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.

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.

Senior Process Scientist needed for gRNA process development. Lead process development and manufacturing oversight for gene therapy programs, specializing in synthetic nucleotide and gRNA development. Requires 5-10 years in biotech with expertise in gene editing and GMP.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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 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.

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.