Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dell’industria farmaceutica e dei Medical Devices? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie alle oltre
Overview In this role you lead AI validation and governance across traditional ML and GenAI/agentic AI, shaping the group’s model risk framework. You provide independent oversight through the full AI lifecycle and stay hands-on with design, validation, and
Would you like to start a new professional adventure as an IT Project Manager (Finance experience) in one of our opportunities in the Finance industry in Milan, Turin, Rome or Bologna ? Your missions? • Lead
Teoresi S.p.A. - 35+ years of history, 8 companies across Italy, the United States, Germany, and Switzerland, 1200+ professionals, 4 acquisitions in a single year, 1 partner, and one comprehensive solution. LOCATION: USA, Michigan We are
POSITION SUMMARY We are looking for a C++ Developer (freelance/P.IVA) to consolidate LivGemini’s existing medical imaging, computational and analytical components into a unified C++ software platform. The selected contractor will be responsible developing a new application
We are seeking an iGaming Platform Quality Engineer to join our team on a contractual basis. The role is fully remote, with occasional travel required to our headquarters in Málaga, Spain. This is 6 months extendable
Role: AI/ML Engineer (Remote) Location: Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking an AI/ML Engineer to work on a Full-Time basis. The role involves developing and deploying machine
Role : Data Specialist (Remote) Location : Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking a Human Data Manager, New Grad to work on a full-time basis. The role
Role: AI Specialist (Remote) Location: Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking an AI Evaluation Specialist to work on a full-time basis. The role involves evaluating AI models
Overview In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional