OverviewExperteer OverviewIn this role you will own process knowledge across the product lifecycle, ensuring robust, validated manufacturing processes.
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You will act as a single point of contact for process knowledge across sites, supporting data-driven decisions and cross-functional collaboration.
You will lead QRAs, monitor critical variables, and drive continuous improvement through CAPAs and product optimization.
You will support product transfers and validation activities, shaping reliable, scalable processes that meet regulatory expectations.
This is a mission-driven role at a global pharma leader focused on patient impact.ResponsibilitiesMaintain process knowledge across the commercial lifecycle and act as SPOCCreate and maintain product-specific Quality Risk Analyses (QRAs)Monitor critical variables via statistical analysis and data trendingEnsure inspection readiness for process aspects of productsTrack product performance, trends, and CAPA-driven improvementsLead/support root cause investigations and cross-functional improvement projectsMaintain ongoing validation state (process, cleaning, verification)Provide data for product transfers and support receiving sites as neededDesign and manage optimization projectsQualificationsDegree xjrgpwk in Pharmacy, Pharmaceutical Technology, Chemistry, Chemical Engineering or equivalent scientific degree6-8 years of experience in Process Support/Process Expert roles within MS&T in a pharmaceutical companyExtensive knowledge of GMP and analytical methods validationExperience with data handling and applied statisticsFluent in English and ItalianNotesRequisiti fondamentali
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