We are seeking a motivated CSV Engineer to join our team. The ideal candidate will be responsible for ensuring that computerized systems are validated in compliance with industry regulations (Gx P, FDA 21 CFR Part 11, EU Annex 11) and internal company procedures. Responsibilities Develop, review, and execute validation documentation (URS, FS, DS, IQ, OQ, PQ, traceability matrices, validation reports, etc. Ensure systems' compliance with applicable regulatory requirement Participate in risk assessments and define validation strategie Provide expertise and support during internal and external audit Liaise with Quality, IT, and business teams to coordinate validation activitie Monitor and maintain validated state of computer systems over their life cycl e Train end-users on relevant procedures and systems,



if require Qualification Bachelor's or Master's degree in Life Sciences, Engineering, Computer Science, or related fie ld Prior experience in computer system validation, preferably in regulated industries (pharma/biotech/medical device s)Strong understanding of Gx P guidelines and relevant regulations (e.g., 21 CFR Part 11, Annex 1 1)Experience with validation of laboratory, manufacturing, or quality syste ms Excellent documentation, organizational, and communication skil ls Ability to work on multiple projects simultaneously and as part of a te #J-18808-Ljbffr

📌 Ingénieur diplômé (Italia)
🏢 EFOR
📍 Italia