Activities Supervise all Manufacturing Activities for production of cosmetics, antisepticand detergent products. Prepare new SOP that related to production activities. Prepare the operation and cleaning SOP for the production equipment. Prepare Batch Manufacturing Record for all products. Prepare the following productsPage 2 of 4 Cosmetics products such as:-Shower GelHand SoapShampooHair OilsHair CreamSkin moisture CreamMassage… Show more Activities Supervise all Manufacturing Activities for production of cosmetics, antisepticand detergent products. Prepare new SOP that related to production activities. Prepare the operation and cleaning SOP for the production equipment. Prepare Batch Manufacturing Record for all products. Prepare the following productsPage 2 of 4 Cosmetics products such as:-Shower GelHand SoapShampooHair OilsHair CreamSkin moisture CreamMassage CreamHair conditionerHair MaskWhiting CreamFacial CleanserHair Waxes Disinfectant and Antiseptic Products such as :-Hand GelHand Sanitizing SolutionSurface Disinfectant SolutionFarm DisinfectantEthyl Alcohol 70%Povidone Iodine Vet. Shampoo Detergent products such as :-Dish wash SoapStain RemoverDegreaser RemoverAutomatic laundry detergentWhite ChloreColor ChloreFloor CleanerClothes Softener and FragranceGlass PolisherAir FresherDescale RemoverAlkaline CleanerAcidic CleanerFlash Training operators on production process. Calculate the yield after each production process (Reconciliation) Calculate the productivity of the production line. Show less

Activities Supervise all Manufacturing Activities for production of antiseptic and disinfectant products.Povidon Iodine 10% AntisepticPovidone Iodine 10% Vaginal DouchePovidone Iodine 1% Mouthwash Povidone Iodine 7.5% Skin CleanserPovidone Iodine 7.5% Surgical ScrubPovidone Iodine 4% Shampoo Hand Gel & Solution SanitizingChlorhexidine Digluconate 4% SolutionO-phthaldehyde 0.55% Solution Ethanol 80% SolutionIsopropyl Alcohol 75% SolutionSavlon… Show more Activities Supervise all Manufacturing Activities for production of antiseptic and disinfectant products.Povidon Iodine 10% AntisepticPovidone Iodine 10% Vaginal DouchePovidone Iodine 1% Mouthwash Povidone Iodine 7.5% Skin CleanserPovidone Iodine 7.5% Surgical ScrubPovidone Iodine 4% Shampoo Hand Gel & Solution SanitizingChlorhexidine Digluconate 4% SolutionO-phthaldehyde 0.55% Solution Ethanol 80% SolutionIsopropyl Alcohol 75% SolutionSavlon Disinfectant Solution Glutaraldehyde 2.5% SolutionEthyl Alcohol 70%Sonar Gel Show less

Establish quality documentation system for INTERPHARM. Issuance and implementation of VMP (Validation Master Plan). Preparing an Annual Product Review (APR). Issue and review process validation protocols with risk assessment. Validation of manufacturing process, review analytical data and issue validation reports with statistical conclusions and recommendation for improvement. Participated in the establishment of new departments and matching them to theGMP.… Show more Establish quality documentation system for INTERPHARM. Issuance and implementation of VMP (Validation Master Plan). Preparing an Annual Product Review (APR). Issue and review process validation protocols with risk assessment. Validation of manufacturing process, review analytical data and issue validation reports with statistical conclusions and recommendation for improvement. Participated in the establishment of new departments and matching them to theGMP. Follow up calibration for all equipments, utilities. Final review Batch Record (Batch Release) and archiving Batch Record. Receiving, review and complete PQ, IQ and OQ for HVAC and water station system. Ensure the implementation GMP and GDP. Participated to prepare formula for new product Disinfectant, Antiseptic and Medical Products. Show less

o Activities Make Trend Analysis for all product 2015 by use Minitab Program. Revision of processing and packaging orders according to approved bill of materials. Issuing Manufacturing and Packaging Batch Records. Revision of the different certificates of each step of the product before moving to the next step.  Final review batch record (Batch Release) and archiving Batch Record. Revision of the different certificates of each step of the product before moving to… Show more o Activities Make Trend Analysis for all product 2015 by use Minitab Program. Revision of processing and packaging orders according to approved bill of materials. Issuing Manufacturing and Packaging Batch Records. Revision of the different certificates of each step of the product before moving to the next step.  Final review batch record (Batch Release) and archiving Batch Record. Revision of the different certificates of each step of the product before moving to the next step. Checking the status of the raw materials in the stores (quarantine , released or rejected) Follow up coding change control and deviation. Follow up processing from receiving raw and packaging materials. Ensure the implementation GMP and GSP. Ensure the implementation Sanitation and Hygiene. Show less

o Activities: Revision of processing and packaging orders according to approved standard order. Preparing batch record and SOPs. Make Internal audit according to ISO 9001/2008, ISO 14001/2004, ISO 18001/2007 and GMP checklist.  Final review batch record. Follow up preparation of sterile eye drops , condition of preparation, sterilization charts for machine parts and garment, particle count for class (A,B,C) and integrity test for filters.  Follow up GMP… Show more o Activities: Revision of processing and packaging orders according to approved standard order. Preparing batch record and SOPs. Make Internal audit according to ISO 9001/2008, ISO 14001/2004, ISO 18001/2007 and GMP checklist.  Final review batch record. Follow up preparation of sterile eye drops , condition of preparation, sterilization charts for machine parts and garment, particle count for class (A,B,C) and integrity test for filters.  Follow up GMP (personal, material, machine and method) and GSP. Show less

o Sterile Eye drops (Ophthalmic)o Sterile Cephalosporin's Area (Parenteral (Vials)) o Solid Dosage Form, Liquid Dosage Form and Central Packaging.o Activities: Follow up environmental of aseptic filling.  Ensure the application of GMP rules application in all production processes and personal hygiene. Review product condition at the various departments. Follow up processing from receiving raw and packaging materials. Supervising the preparation process step… Show more o Sterile Eye drops (Ophthalmic)o Sterile Cephalosporin's Area (Parenteral (Vials)) o Solid Dosage Form, Liquid Dosage Form and Central Packaging.o Activities: Follow up environmental of aseptic filling.  Ensure the application of GMP rules application in all production processes and personal hygiene. Review product condition at the various departments. Follow up processing from receiving raw and packaging materials. Supervising the preparation process step by step & ensure following the steps of the MBR. Make the routine tests during the production process according to the SOP. Revision of the different certificates of each step of the product before moving to the next step. Follow up Line clearance according to GMP rules for all production lines. Withdraw samples for testing and retain samples from production areas. Review the quantities, batch no., and right labels of the finished product before deliver it to the warehouse. Checking the log books for processing, balances calibration& cleaning in the production area. Checking the status of the raw materials in the stores (quarantine , released or rejected) Ensure the application of GSP rules (coding &recording of raw materials, storage conditions, transportation of raw materials in the stores, cleaning procedures, recording temp & humidity in the stores personnel gowning…etc.) Show less

Working at Laboratory El-Nour El-Fatemy for Medical Analysis and Blood Researching and Virology