192 English-speaking jobs in Emilia-Romagna

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 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 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.

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.

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.

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.

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.

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 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.

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.

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, 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.

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.

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, 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.

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

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.

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.