In the frame of a maternity replacement, You should manage several Compliance related aspects in order to ensure that products produced in the site and materials used and /or product meet the appropriate Quality Standards in Line with Company, cGMP requirements as well registration files: deviation management and related timely and effective investigation management including a follow up on CAPA plans; encourage a continuous improvement culture, and review of the relevant documentation (e.g. validation protocols, reports and investigations carried out during processing problems and deviations). Who you are: Scientific degree (e.g., Pharmacy, Biology or Chemistry)Languages: Fluent in Italian and EnglishExperiences: less than 1 years’ experience in the pharmaceutical industry. Knowledge of Quality systems (e.g. Quality Risk Management, Deviations, Aseptic techniques, Root Cause Analysis, CAPA management, Validation skills) is a plus.Job related skills & Knowledge: Good inter-personnel relationship inside the plant and prompt reaction to problemsProfound customer-orientation with an eye for the company’s own interestsFlexibility and keen pursuit of innovation throughout all processes in the continuous search of sustainable new ideasStrong desire to develop and grow by way of taking responsibility and engaging in additional tasks and operations