Validation Or Lavori In Siena Tos - 30 Job Positions Available

Pramac, parte di Generac, cerca un Project Engineer per unirsi al team di Ingegneria presso la sede di Casole dElsa (Siena). Compito principale: gestire lo stato avanzamento progetti e guidare miglioramenti del prodotto, assicurando la soddisfazione

Process & Computer System Validation Specialist (GCP) Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti‑tumor therapies, is looking for a highly motivated and qualified Process

A leading biotech company in Italy is seeking a highly motivated Process & Computer System Validation Specialist (GCP) to join their QA department. The role involves validating computerized systems to ensure compliance with GMP/GCP regulations, contributing to

Pramac, part of Generac, is seeking a Project Engineer to join the Engineering Team at our Casole dElsa headquarters in Siena, Italy. You will manage all technical aspects of products, drive improvements, and ensure customer satisfaction

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

Direct message the job poster from Philogen S.p.A. Philogen S.p.A. is a biotechnology company whose mission is the development of biologic products for the imaging and therapy of life‑threatening diseases, with a strategic focus on cancer

Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is looking for a highly motivated and qualified GMP Quality Assurance Specialist ” who will

Role : Human Data Specialist (Remote) Location : Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking a Senior Human Data Manager to work on a full-time basis. This role

Siamo Humans.tech. Creiamo interfacce intelligenti che risolvono tematiche complesse e migliorano esperienze, oltre a essere, ovviamente, belle! Collaboriamo con aziende globali come Airbnb , Amazon , Angelini … e siamo solo alla lettera A. In 10

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

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

Project Engineer page is loaded# Project EngineerPresenta candidaturalocations: Casole dElsa, Italytime type: A tempo pienoposted on: Offerta pubblicata oggijob requisition id: JR15614 S iamo Pramac, unazienda Generac, leader nellevoluzione verso soluzioni energetiche più resilienti, efficienti e

# Project EngineerApplylocations: Casole dElsa, Italytime type: Full timeposted on: Posted Yesterdayjob requisition id: JR15614 We are Pramac, a Generac Company, leading the evolution to more resilient, efficient, and sustainable energy solutions. Established in 1966, we

Overview In this backend-focused role, you will help build and scale Deel’s APIs and services used by global customers. You’ll work with cross-functional teams to design robust features, optimize performance, and ensure a customer-centric engineering approach.

Overview As Metrology Manager at Sanofi’s Goa GMP site, you lead the site-wide metrology and calibration program to ensure instruments stay accurate, traceable and compliant. You will collaborate with Engineering, Quality, Validation and Manufacturing to maintain calibration

Overview In this role you will support the deployment of Manufacturing/Warehouse Execution capabilities within the Transcend SAP S/4HANA program. You work closely with cross-functional teams to validate data, configure solutions, and ensure alignment with the global

Overview As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and