About Soufiane
French
Native or bilingual
Arabic
Native or bilingual
English
Fluent
Experience
- Hitachi EnergyConsultant SME Quality ManagementOctober 2022 - September 2023 (11 months)Charleroi, Belgium-Deployment of a new Quality process flow-Collaboration with various contacts at Hitachi sites worldwide-Review of the entire quality department database-Manage the QM module of SAP REIWA and the QM of the DPS DIGITAL passport system-Management of major defects and minor deviations-Integration of all SAP REIWA quality management functions-Writing specifications and procedures Data migration Review All of Preload and Post load files, Inspection plan, inspection lot, Quality info record, Integration and Creation of work center Manage deployment of SAP S/4 HANA “REIWA” Quality management and DPS DIGITAL passport system QM.-Deployment Training for USERS, Coaching communication Follow-up and resolution of technical problems Manage defect major and minor deviations.-Deployment PPAP Notification Creation, requirement Drafting of specification. Integration of all SAP REIWA S4 HANA quality management functions QM Review the quality database. Collaboration with different contact persons at Hitachi sites around the world and Solution designers Infosys
- Lonza AGConsultant Technical Services SMEPHARMACEUTICALS INDUSTRYMay 2022 - September 2022 (4 months)Verviers, BelgiumAnalysis of the existing situation-Change management, Lean management-Coordination and information sharing - Planned changes-Task planning in collaboration with impacted departmentsAddition of the UDI field (barcode on labels)-Software Changes Deployment: replacement of Access and Codesoft 9 with Nicelabel software-Revision and standardization of all other Lonza labels-Coordination and data sharing with the Lonza US site in Walkersville-Consider an action plan-Plan and organize training test new printers- Test, Printer Qualification,-Writing and introduction of the Change Request CRB/URS user requirement specification-Ensure IT data integrity
- CatalentConsultantMEDICALJanuary 2022 - March 2022 (2 months)Bruxelles, BelgiumRemediation project following an FDA inspection Baseline assessment of quality systems Periodic audits, manufacturing oversight and batch record review and approval. Review and evaluation of deviations from calibration and preventive maintenance, facilities The review and evaluation of production procedures, dressings, qualifications and validations of vision systems and visual inspection of syringes
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Education
- Specialized Master's Degree, Manager of Continuous Improvement and Industrial PerformanceEI.CESI - Engineering School of CESI2016Mastère Spécialisé, Responsable Amélioration Continue et Performance Industrielle
- Master's degree, Industrial Systems Engineering specializing in Production Systems Management and LogisticsUniversity of Lorraine2015Master's degree, Génie des Systèmes Industriels option gestion des systèmes de production et Logistique
Certifications
- GREEN BELT LEAN SIX SIGMACESI2016