Job Description Summary-Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. Prepare Documentation for Batch Release of commercial PharmaceuticalsJob DescriptionMajor accountabilities: Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person – Executes batch release in compliance with registration -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)Key performance indicators: On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand -Successfully support continuous improvement projects -Executes batch release in compliance with registration Minimum Requirements: Work Experience: Functional Breadth.QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &.Collaborating across boundaries.cleanliness zones.Skills: Continuous Learning.Dealing With Ambiguity.Gmp Procedures.Qa (Quality Assurance).Quality Control (Qc) Testing.Quality Standards.Self Awareness.Technological Expertise.Technological Intelligence.Languages :English.Skills DesiredContinued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological IntelligenceSummaryLocation: Milano; RemoteType: Full time