o Responsible to manage Receiving Inspection team, inspecting incoming parts, quality papers, performing R&D measurements requests. Generating Inspection Reports.o Microbiology and Environmental monitoring SME. Responsible for Environmental monitoring process (results approval, related deviations, changes in clean room, clean room validation and etc.). Procedures and process improvements in the clean rooms (ISO 7 and ISO 8). Handling all the microbiology related manufacturing deviationo Member of NCR and CAPA team. Handling and investigating of manufacturing deviations, member of MRB.o Quality projects management- implementation of new processes.o Training of employees in relevant fieldso Support in QA and RA projects

o Leading QC-OEM team. Receiving Inspection, In Process inspection, final inspection.o Preparation all quality paperwork, including COC/COA of product.o Handling suppliers negotiation.o Member of MRB, participating in NCRs investigation, supplier evaluation.o Masters approver. Member of FDA audit preparation team.

• Outside warehouses auditor/evaluation team member.