Mohamed Abd El Moniem
About
Mohamed Abd El Moniem is from Saudi Arabia. Mohamed works in the following industries: "Cosmetics". Mohamed is currently Production Manager at Modern Beauty for investment, located in Riyadh, Saudi Arabia. In Mohamed's previous role as a Production Manager at Vona Pharma, Mohamed worked in Al-Riyadh Governorate, Saudi Arabia until Feb 2020. Prior to joining Vona Pharma, Mohamed was a Production Manager at Suncare pharma and held the position of Production Manager at Al-Kharj Governorate, Saudi Arabia. Prior to that, Mohamed was a Senior Production Specialist at DABUR EGYPT LIMITED, based in Egypt from Sep 2010 to Mar 2016. Mohamed started working as Senior Production Specialist at Adwic - El Nasr Pharmaceutical Co. in Egypt in Sep 2007. From Sep 2004 to Sep 2007, Mohamed was Production Specialist at Waki Pharma, based in Egypt.
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Mohamed Abd El Moniem's current jobs
• Rolled out online registration at E-Cosma, Ghad and Saber platforms. • Collect Required Documents For MDEL, MDNR to Registry in MDIL and CIMD to get MDMA Certification and get free sales Certificate of Medical Devices, Specially Cosmetics Contact lenses. • Review implementing Rules of MD, Requirements and Conditions, SASO, ISO, SFDA Standers to Communicate with suppliers to avoid any malfunction in receiving the shipment. • Contacting suppliers to get the best prices and highly quality to obtain the rights of partnerships as exclusive agency or distributor for their products. • Contact with USA, Poland, Korean, China OEM companies to produce our Private brands. • Contact with a specializing companies in automatic equipment used for cosmetics manufacturing to know the budget prices for new project were planning.
Mohamed Abd El Moniem's past jobs
Renovation of Raw materials, equipment and processes. Prepare pre-qualification requirements and questionnaires to writing RFPs, RFQs documentation package and technical Data and running an RFI to select an RFQ winner for production lines of plastic factory (Bottles&Caps) and Cosmetics & Detergents chemical & Microbiology laboratories and utilities (RO water purification unit, waste water treatment unit, steam boiler, Air compressors, power station and HVAC system), production area desging and supervision of Construction works and ERP system. Established SOPs in performance of job and adheres consistently to GMPs. Established QA/QC, Auditing, Validation and production planning systems. Established R&D Team to originate new products in concert with customer needs and business model.
• Develop new products formula and improve products formula (Simple Syrups , Suspensions , Mouth Wash , Antiseptic Solutions , Lotions , Emulsions , Creams , Ointments & Suppositories) • Established Quality systems, (QA & C. functions) as cGMP, FDA & regulatory std. Quality Review, Vendor dev., preparation of related SOP’s, Stability Studies, and preparation of Validations protocols & Reports. • Follow-up to all acts of quality control and production department. • Product registration in SFDA (E COSMA). • SFDA Regulatory Affairs.
Responsible for numerous production lines with various speed ie.120 BPM/120PCS. Control and effectively use production capacity, equipment, manpower and outside resource through planning, organizing and scheduling to minimize losses. Manage and ensure the reduction in spoilage or wastage where and when Possible. Analyzing Processes / applications & recommending Process modifications to enhance Operational efficiency. Training Program Conduction related of the operation, quality aspects like GMP, HACCP, 5S, TPM, TQM and ERP. Apply the QMS to find out the areas of rejection, failures and take corrective action, plan preventive Action accordingly. Responsible for daily MIS Reporting to production manager. Ensuring compliance with the production and dispatch plans by minimizing breakdowns and wastages in the packing section. Ensuring maximum efficiency of the packing machines in consultation with the packing engineer to minimize breakdown and down time. Reviewed company operations - evaluated their efficiency, effectiveness and compliance with procedures.
Ensure cGMP procedures are reviewed and staff is training on relevant curricula Facilitate technical transfer of company processes to manufacturing. Review and approve batch records, change controls and project plans Coordinate with different departments to ensure the production priorities and ensure that the required raw material is available to deliver products in time. Supports investigations and is involved with CAPA recommendations Delegate or lead the writing of deviations, planned variance, change control forms or CAPAs as required Participate in production and planning meetings as requested
Supervises the day-to-day production, safety, scheduling, staffing, material management, compliance, training and auditing activities – to meet customer requirements including deadlines, quality, GMP and FDA standards. Represents the company during FDA inspections; provides information as necessary to FDA that establishes credibility and demonstrates compliance with cGMPs. Reviews, approves, and manages documentation for batch and system records; assists in release of product for distribution; assists in meeting product release time goals.