186 English-speaking jobs in Emilia-Romagna

Senior Firmware Engineer to develop and maintain embedded software for GNSS receiver products. Requires 5+ years in embedded development, strong C/C++ skills, and experience with embedded Linux.

Hands-on System Test Engineer to validate advanced construction and machine control technologies in real field conditions. Test hardware, firmware, and software releases, troubleshooting technical issues with international teams. Requires experience in testing or field support.

Senior Software Engineer specializing in Field Survey Applications using C++. Develop cross-platform software for Windows, Linux, Android, and iOS, integrating with field devices like GNSS receivers. Requires 3+ years of C++ experience.

Field Service Specialist to diagnose and resolve technical issues for Foundation Equipment. Responsibilities include installation, troubleshooting hydraulic/electrical systems, and providing customer training. Requires 3+ years of experience and technical knowledge.

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.

Trevi S.p.A. seeks Helpers for construction sites in Italy. Responsibilities include manual labor, drilling, excavation, and concrete pouring. Duties involve assisting with equipment positioning, loading/unloading materials, and maintaining a clean workplace while following all safety procedures.

Field Service Specialist to diagnose and resolve technical issues for Foundation Equipment. Responsibilities include installation, troubleshooting hydraulic/electrical systems, and providing customer training. Requires 3+ years of experience and technical knowledge.

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.

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.

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.

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.

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.

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, 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.

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.

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.

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.