Site Documentation

Manens S.p.A. cerca una risorsa per l’ufficio Direzione Lavori a Salerno, con ruolo di supporto alla gestione documentale del cantiere e al coordinamento con il Direttore dei Lavori e i cantieri.Si richiede diploma o laurea in ingegneria, almeno 3 anni di esperienza in cantieri complessi, conoscenza della normativa di settore e uso del pacchetto Office....

Manens S.p.A. cerca una risorsa per l’ufficio Direzione Lavori a Salerno, con ruolo di supporto alla gestione documentale del cantiere e al coordinamento con il Direttore dei Lavori e i cantieri.Si richiede diploma o laurea in ingegneria, almeno 3 anni di esperienza in cantieri complessi, conoscenza della normativa di settore e uso del pacchetto Office....

Manens S.p.A. cerca una risorsa per l’ufficio Direzione Lavori a Salerno, con ruolo di supporto alla gestione documentale del cantiere e al coordinamento con il Direttore dei Lavori e i cantieri.Si richiede diploma o laurea in ingegneria, almeno 3 anni di esperienza in cantieri complessi, conoscenza della normativa di settore e uso del pacchetto Office....

Overview In this role you will lead on-site installation, commissioning and testing of LV/MV power-system equipment, ensuring full operation per project requirements. You will collaborate with internal teams and partner suppliers to validate performance, support after-sales activities, and generate detailed commissioning and final status reports. You will...

Sr. Site Contracts Associate IQVIA Biotech Italy - HomebasedOverviewWe are seeking an experienced Senior Site Contracts Associate to manage contract strategy and oversee all start‑up contracting activities for selected sponsors. In this role, you will support complex studies and multi‑protocol programs, ensuring high‑quality delivery and operational...

Overview As an RSU Specialist, you will lead country-specific site activation and regulatory activities within IQVIA's FSP team in Italy. You will act as the primary liaison for investigative sites and project teams, ensuring compliant, timely site activation and regulatory documentation. You will leverage local regulatory expertise to support timelines,...

OverviewAs a Principal Medical Writer, you will lead high-quality scientific documents to support regulatory submissions and publications. You collaborate with clinical, regulatory, and medical affairs teams to translate data into clear narratives. The role is on-site in a collaborative environment that values expertise and innovation. You will shape...

Overview In this role you will lead and optimize the Quality Management System to ensure GMP, FDA and EU compliance across the site. You will partner with cross-functional teams to drive quality improvements, manage inspections, training, and documentation, and report on QMS performance. You will enable a culture of quality and continuous improvement,...

Overview Senior Electrical Engineer in Milan leading electrical design, coordination, and site execution for a data centre project. You will drive technical leadership, ensure compliance with standards, and oversee testing, commissioning, and safety. You’ll collaborate with cross-functional teams to integrate LV/MV systems and deliver a mission-critical...