Mohamed Mousa Email & Phone Number

Saudi Arabia

Riyadh, Saudi Arabia

• 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.

Al-Riyadh Governorate, Saudi Arabia

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.

Al-Kharj Governorate, Saudi Arabia

• 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.

Egypt

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.

Egypt

Ensure cGMP procedures are reviewed and staff is training on relevant curriculaFacilitate technical transfer of company processes to manufacturing. Review and approve batch records, change controls and project plansCoordinate 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 recommendationsDelegate or lead the writing of deviations, planned variance, change control forms or CAPAs as requiredParticipate in production and planning meetings as requested

Egypt

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.