Job descriptionHands-on experience in GMP-compliant manufacturing environmentExposure to regulatory audits (e.g. USFDA, MHRA, WHO).Deep understanding of GMP, ICH guidelines, and local / international regulatory requirementsSkilled in preparing for and facing customer audits.Root cause analysis, CAPA implementation, and continuous improvementFamiliarity with QMS software, oracle, SAP, Minitab, LIMS, and other electronic documentation systems.Involvement in quality systems : deviations, CAPA, change control, and batch releaseExperience in document control & validationsManaging QA teams, mentoring staff, and cross-functional collaboration