Csv Specialist

Pubblicato il 04-11-2026 · BSP Pharmaceuticals · Provincia di Latina

BSP Pharmaceuticals S.P. A is focused on the development and manufacturing of anticancer drugs with high potency and cytotoxitc characteristics for the Pharmaceuticals Industry.Se i requisiti e l'esperienza richiesti per questo lavoro corrispondono alle sue competenze, la preghiamo di candidarsi tempestivamente.BSP has been at the forefront in the fight agains cancer since 2006.Innovation is the hallmark of BSP with investments in new technologies and production methods in a high containment plant.We are one of the most important Contract Development and Manufacturing Organization (CDMOs) for anticancer drugs.The fight against cancer is ours too.To expand its workforce, BSP Pharmaceuticals is seeking candidates for opportunities within the CSV & Data Integrity areaResponsibilities:Drafting and execution of validation documents for laboratory and production computer systems (analytical instrumentation, HMI,



SCADA...)Validation PlanSystem ConfigurationValidation protocols (IQ/OQ/PQ)Traceability MatricesReportsPerforming testing activities of laboratory and production computerized systems.Performing periodic reviews of computerized systemsParticipation in SAT and FATCollaboration in writing departmental SOPs and the Validation Master Plan for computerized systemsRequisitiExperience in Computer System ValidationMaster's degree in a scientific disciplinesThorough knowledge of 21 CFR Part 11 and Annex 11 regulations and Data Integrity principles. xysqume At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect the diversity, the different backgrounds and experiences and provide equal opportunity for all.#J-18808-Ljbffr
Max. 8 MB. Formati Accettati: PDF, RTF, DOC, DOCX, ODT.