203 English-speaking jobs in Emilia-Romagna

Senior System Test Engineer to lead testing of Construction and Machine Control solutions. Plan bench, lab, and field testing, investigate technical issues, and collaborate with global teams. Requires QA/system testing experience and strong analytical skills.

Embedded Software Test Engineer to support testing and validation of advanced GNSS products for construction, geospatial, and agriculture. Requires a degree in related fields or Geometra diploma, plus practical experience with survey-grade GNSS equipment.

Senior Software Engineer to develop field survey applications using Java and C++. Develop and maintain software for GNSS receivers and surveying equipment across multiple platforms. Requires 3+ years of experience and strong OOP skills.

Financial Controller supporting the Core Markets Business Unit. Responsibilities include month-end/year-end close, financial reporting, planning, and performance monitoring across international markets. Requires 4+ years in international finance.

Provide legal support to Staff and Global R&D functions, including contract drafting, negotiation, and risk evaluation. Responsibilities cover finance, procurement, sustainability, and clinical/preclinical studies. Requires a Master's in law and 2-3 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.

Manage GCP compliance, CAPAs, and quality metrics within Global R&D. Execute first and second-party audits and finalize quality documents. Requires 3+ years in Pharma/CRO QA with strong GCP knowledge.

Manage training and documentation across Global TechOps & Supply. Oversee EDMS, training systems, and document control, ensuring regulatory compliance. Requires 5+ years in pharma QA with scientific degree.

Senior Process Scientist needed for gRNA process development. Lead process development and manufacturing oversight for gene therapy programs, focusing on in vivo LNP programs. Expertise in gRNA development, synthetic nucleotide manufacturing, and CRO/CDMO management is required.

Senior Manager to drive R&D digital transformation by designing and implementing data-driven processes using platforms like Veeva Vault. This role orchestrates process excellence, digital innovation, and change management across functions.

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 Regulatory Writer for Global Rare Diseases. Author, review, and manage regulatory documents for global health authorities, translating clinical and CMC data into compliant submissions across the product lifecycle.

Manage the Pharmacovigilance System Master File (PSMF) and ensure compliance with regulatory requirements. Evaluate guidelines, update PSMF documentation, define KPIs, and report on PV system performance. Requires a Master's degree and 5+ years in international Pharmacovigilance.

Lead global post-marketing pharmacovigilance operations, ensuring data quality and compliance for Chiesi's portfolio. Oversee safety data collection, literature review, and stakeholder engagement.

Senior Clinical Project Manager coordinates operational management for assigned projects to develop compounds. Responsibilities include managing clinical trials, CRO oversight, budget adherence, and ensuring compliance with SOP and GCP.

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.

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 Technical Leader for GRD CMC is accountable for CMC development and IMP supply strategy from nomination to commercial launch. Requires 10+ years in pharma, experience with regulatory interactions (EMA/FDA), and leadership of internal/external teams.

Manage pharmacovigilance operations for interventional clinical trials, ensuring compliance with PV legislation. Support safety data collection, process maintenance, and CRO oversight within R&D. Requires a Master's degree and 3+ years in Pharmacovigilance or Clinical Research.

Manage inspections, training, documentation, and site compliance for the Quality Management System. Ensure GMP adherence to FDA and EU regulations while improving quality KPIs. Requires a scientific degree and 5+ years in pharma QA/Production.