This document is a curriculum vitae that summarizes the professional experience and qualifications of Saeed Adel El-sayed. It outlines his education credentials which include a Bachelor's degree in chemistry and biochemistry from Helwan University in Egypt. It also lists his work experience in water treatment and quality control roles for Nestle Waters Jeddah and as a chemist for a beverage company in Egypt. His responsibilities and skills include chemical, physical, and microbiological analysis, quality control systems, and process supervision.
Biological indicators for /certified fixed orthodontic courses by Indian dent...Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and offering a wide range of dental certified courses in different formats.
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Bionext Pharma Pvt. Ltd., a dedicated manufacturing facility for Liquid Orals is pledged to Ethics for manufacturing of quality drug products that consistently meet the standards by adhering to current Good Manufacturing Practices (cGMP) in its facility, it also endeavors to delight the customers through its unique and cost effective formulations and timely quality services? .
Biological indicators for /certified fixed orthodontic courses by Indian dent...Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and offering a wide range of dental certified courses in different formats.
Indian dental academy provides dental crown & Bridge,rotary endodontics,fixed orthodontics,
Dental implants courses.for details pls visit www.indiandentalacademy.com ,or call
0091-9248678078
Bionext Pharma Pvt. Ltd., a dedicated manufacturing facility for Liquid Orals is pledged to Ethics for manufacturing of quality drug products that consistently meet the standards by adhering to current Good Manufacturing Practices (cGMP) in its facility, it also endeavors to delight the customers through its unique and cost effective formulations and timely quality services? .
Microbial analysis of water system and endotoxin estimationashapatel676
In Pharmaceutical different grades of waters are used and they all must be tested firest before using it for manufacturing any products. Products sometimes get contaminated because of presence of endotoxins so they mus be checked by performing BET test
Commercializing antibody-drug conjugates: a CMO’s journeyMerck Life Sciences
Watch the webinar here: https://bit.ly/2YLDzTE
This webinar will take you through the story of a CMO preparing for the manufacture of a Commercial Antibody Drug Conjugate (ADC).
Join us to learn about how we grew as a CMO to develop a Commercial ADC program. We will walk through the full timeline from development, process risk assessment and control strategy development and validation, finishing off with preparation for a Commercial ADC Pre-Approval Inspection Audit.
In this webinar you will learn how to:
• Properly structure your development work
• Perform a thorough process risk assessment
• Prepare for pre-approval inspection
EU GMP Annex 1 Draft: Implications on Sterilizing Grade Filter ValidationMilliporeSigma
Watch the presentation of this webinar here: https://bit.ly/3kk0Qs1
In this webinar, you will learn:
- About the GMP Annex 1 draft regulatory overview
- How to incorporate the integrity testing & PUPSIT in the filtration systems validation
- How to design a bacterial retention test in terms of organism selection and single vs multiple use validation
Detailed description:
In this webinar we will discuss the implications of the EU GMP Annex 1 draft on the filtration of medicinal products and how this impacts the validation studies.
Bacterial Retention Testing is a critical part of the manufacturing validation process and is required by all regulatory bodies worldwide. Using case studies, our experts will explain how the Annex 1 draft is incorporated into the filtration systems validation exercise, specifically for integrity testing & PUPSIT (Pre-Use Post Sterilization Integrity Testing), the selection and justification of the appropriate test organism, and validation implications of single versus multiple use.
Validation may be defined as
“ Establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality attributes.”
Dry Heat
Moist Heat
Gas (Ethylene oxide)
Radiation (Gamma or Electron)
Filtration
Others - UV, Steam and formaldehyde, hydrogen peroxide
Quality by Design Principles Applied to Sterilizing Filtration by Michael PayneMilliporeSigma
Key regulatory documents and regulatory thinking now includes quality by design (QbD). This webinar focuses on how to integrate practical QbD activities into the process and analytical aspects of sterile medicinal product sterilizing filtration and qualification.
In this webinar, you will learn to:
• Focus on practical QbD terms and approaches
• Highlight critical product quality aspects of sterile medicinal products
• Develop design and control spaces for sterilizing filtration
• Easily integrate QbD into the process and analytical operations in early phase development and into manufacturing phase production
Abstract:
Final sterilizing filtration is the last operation in downstream processing to assure the sterility of medicinal products. Poorly defined product attributes process parameters may attract regulatory scrutiny, affect final product sterility and patient safety. A better understanding of QbD concepts and principles allows for better process and analytical monitoring and control at both early and final phase production. The webinar will show how currently available process cGMP information can be practically incorporated into QbD product quality attributes and process parameters. This is especially vital for the third party conducted laboratory work such as bacterial retention and leachable studies.
Next-Generation Bioprocessing Monitoring to Enable Smart Data Management and ...MilliporeSigma
Watch this webinar here: https://bit.ly/2ZpV3GU
Biopharmaceutical processes are complex and highly variable in nature. This can result in inconsistent and unpredictable process outcomes. To manage complexity and better understand causes of variability, in-depth knowledge and thorough understanding of the process is critical. Bio4C™ ProcessPad provides the data integration, analysis and sharing across the manufacturing network and end-to-end data management throughout the process lifecycle required for continued process verification, reporting, and analytics.
Bio4C™ ProcessPad is a data visualization, analytics, and process monitoring platform that enables bioprocess lifecycle management, reporting, investigations, and continued process verification (CPV). Intelligently combining process data from batches, Enterprise Resource Planning (ERP), Manufacturing Execution System (MES), Laboratory Information Management System (LIMS), Historian, process equipment, and manual sources into a single, validated data source, Bio4C™ ProcessPad ensures data is current, complete, and contextual throughout the product lifecycle.
In this webinar, you will learn:
• Introduction to Next Generation BioContinuum™ Digital Platform and Bio4C™ Software Suite
• Overview of Bioprocess lifecycle and present biomanufacturing data management challenges
• Introduction to the Bio4C™ ProcessPad digital platform and its modules and features
• Benefits of Bio4C™ ProcessPad in investigations, process monitoring, continued process verification (CPV) and CDMO operations
Describes Megan Rose (Pr.Sci.Nat.) an employee at Neopak R&D, situated in Cape Town, South Africa. Contact details are given. Neopak Research and development. Neopak RnD.
I am Seeking an opportunity in gulf area & Egypt , multinational organization
where I can gain practical experience and develop my skills to achieve professional and personal targets.
I have got advanced experiences at QMS ( ISO9001-ISO17025- ISO22000 / HACCP ) and processes establishing, compliance verification and systems auditing
Quality and Food Safety Auditor, GLP, GMP, Hygiene.
. I am14 year Experienced in Quality, HSE, R&D & Manufacturing Operations , Exposure in Multiproduct category i.e Pure natural Mineral water , Juices Beverages,Dairy, Fruit & Vegetable canning, Tomato concentrate processing,
I am Seeking an opportunity in Gulf area & Egypt , multinational organization where I can utilize my experience and my skills to enrich and develop my professional and personal targets."
A Dynamic Professional with over 14 years’ experience in Quality Management, Food Safety & Lab & CHAMICAL & MicrobiologyFOOD, innovation Management, , Cost saving & Supplier Development, Packaging Development, Co- manufacture & Co-Pacer Health and Nutrition, Food Regulations, Crisis Management, Contours improvement and People Management, leadership management, Team work
Expert in Quality Management Systems, GMP, HACCP,ISO 22000, Crisis Management,Risk Assessment,, Innovation, Management, Consumer Complaint, Product & Process Validation & Supplier development & Compliance and Regulatory
Smooth functioning of Microbiology section. Ensure quality of analytical tests performed. Provides technical assistance to market on Microbiology issues
Microbial analysis of water system and endotoxin estimationashapatel676
In Pharmaceutical different grades of waters are used and they all must be tested firest before using it for manufacturing any products. Products sometimes get contaminated because of presence of endotoxins so they mus be checked by performing BET test
Commercializing antibody-drug conjugates: a CMO’s journeyMerck Life Sciences
Watch the webinar here: https://bit.ly/2YLDzTE
This webinar will take you through the story of a CMO preparing for the manufacture of a Commercial Antibody Drug Conjugate (ADC).
Join us to learn about how we grew as a CMO to develop a Commercial ADC program. We will walk through the full timeline from development, process risk assessment and control strategy development and validation, finishing off with preparation for a Commercial ADC Pre-Approval Inspection Audit.
In this webinar you will learn how to:
• Properly structure your development work
• Perform a thorough process risk assessment
• Prepare for pre-approval inspection
EU GMP Annex 1 Draft: Implications on Sterilizing Grade Filter ValidationMilliporeSigma
Watch the presentation of this webinar here: https://bit.ly/3kk0Qs1
In this webinar, you will learn:
- About the GMP Annex 1 draft regulatory overview
- How to incorporate the integrity testing & PUPSIT in the filtration systems validation
- How to design a bacterial retention test in terms of organism selection and single vs multiple use validation
Detailed description:
In this webinar we will discuss the implications of the EU GMP Annex 1 draft on the filtration of medicinal products and how this impacts the validation studies.
Bacterial Retention Testing is a critical part of the manufacturing validation process and is required by all regulatory bodies worldwide. Using case studies, our experts will explain how the Annex 1 draft is incorporated into the filtration systems validation exercise, specifically for integrity testing & PUPSIT (Pre-Use Post Sterilization Integrity Testing), the selection and justification of the appropriate test organism, and validation implications of single versus multiple use.
Validation may be defined as
“ Establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality attributes.”
Dry Heat
Moist Heat
Gas (Ethylene oxide)
Radiation (Gamma or Electron)
Filtration
Others - UV, Steam and formaldehyde, hydrogen peroxide
Quality by Design Principles Applied to Sterilizing Filtration by Michael PayneMilliporeSigma
Key regulatory documents and regulatory thinking now includes quality by design (QbD). This webinar focuses on how to integrate practical QbD activities into the process and analytical aspects of sterile medicinal product sterilizing filtration and qualification.
In this webinar, you will learn to:
• Focus on practical QbD terms and approaches
• Highlight critical product quality aspects of sterile medicinal products
• Develop design and control spaces for sterilizing filtration
• Easily integrate QbD into the process and analytical operations in early phase development and into manufacturing phase production
Abstract:
Final sterilizing filtration is the last operation in downstream processing to assure the sterility of medicinal products. Poorly defined product attributes process parameters may attract regulatory scrutiny, affect final product sterility and patient safety. A better understanding of QbD concepts and principles allows for better process and analytical monitoring and control at both early and final phase production. The webinar will show how currently available process cGMP information can be practically incorporated into QbD product quality attributes and process parameters. This is especially vital for the third party conducted laboratory work such as bacterial retention and leachable studies.
Next-Generation Bioprocessing Monitoring to Enable Smart Data Management and ...MilliporeSigma
Watch this webinar here: https://bit.ly/2ZpV3GU
Biopharmaceutical processes are complex and highly variable in nature. This can result in inconsistent and unpredictable process outcomes. To manage complexity and better understand causes of variability, in-depth knowledge and thorough understanding of the process is critical. Bio4C™ ProcessPad provides the data integration, analysis and sharing across the manufacturing network and end-to-end data management throughout the process lifecycle required for continued process verification, reporting, and analytics.
Bio4C™ ProcessPad is a data visualization, analytics, and process monitoring platform that enables bioprocess lifecycle management, reporting, investigations, and continued process verification (CPV). Intelligently combining process data from batches, Enterprise Resource Planning (ERP), Manufacturing Execution System (MES), Laboratory Information Management System (LIMS), Historian, process equipment, and manual sources into a single, validated data source, Bio4C™ ProcessPad ensures data is current, complete, and contextual throughout the product lifecycle.
In this webinar, you will learn:
• Introduction to Next Generation BioContinuum™ Digital Platform and Bio4C™ Software Suite
• Overview of Bioprocess lifecycle and present biomanufacturing data management challenges
• Introduction to the Bio4C™ ProcessPad digital platform and its modules and features
• Benefits of Bio4C™ ProcessPad in investigations, process monitoring, continued process verification (CPV) and CDMO operations
Describes Megan Rose (Pr.Sci.Nat.) an employee at Neopak R&D, situated in Cape Town, South Africa. Contact details are given. Neopak Research and development. Neopak RnD.
I am Seeking an opportunity in gulf area & Egypt , multinational organization
where I can gain practical experience and develop my skills to achieve professional and personal targets.
I have got advanced experiences at QMS ( ISO9001-ISO17025- ISO22000 / HACCP ) and processes establishing, compliance verification and systems auditing
Quality and Food Safety Auditor, GLP, GMP, Hygiene.
. I am14 year Experienced in Quality, HSE, R&D & Manufacturing Operations , Exposure in Multiproduct category i.e Pure natural Mineral water , Juices Beverages,Dairy, Fruit & Vegetable canning, Tomato concentrate processing,
I am Seeking an opportunity in Gulf area & Egypt , multinational organization where I can utilize my experience and my skills to enrich and develop my professional and personal targets."
A Dynamic Professional with over 14 years’ experience in Quality Management, Food Safety & Lab & CHAMICAL & MicrobiologyFOOD, innovation Management, , Cost saving & Supplier Development, Packaging Development, Co- manufacture & Co-Pacer Health and Nutrition, Food Regulations, Crisis Management, Contours improvement and People Management, leadership management, Team work
Expert in Quality Management Systems, GMP, HACCP,ISO 22000, Crisis Management,Risk Assessment,, Innovation, Management, Consumer Complaint, Product & Process Validation & Supplier development & Compliance and Regulatory
Smooth functioning of Microbiology section. Ensure quality of analytical tests performed. Provides technical assistance to market on Microbiology issues
The all the content in this profile is completed by the teachers, students as well as other health care peoples.
thank you, all the respected peoples, for giving the information to complete this presentation.
this information is free to use by anyone.
Agricultural Commodity Analysis and Trade Issues for ShippingMathew Conoulty
David Conoulty of Commodity Inspection Services outlines the various factors involved with testing for the quality of agricultural commodities during the shipping process. The presentation covers the analysis process, the reliability of results, analytical methods and the improved equipment used to perform quality laboratory analysis.
I am working at Best Cheese Company Kaliob (Lactel & Nestle Egypt) for dairy product as a Food Technologist with the mission of Product & industrial performance development.
STANDARD OPERATING PROCEDURES FOR PARENTERAL DOSAGE FORM PREPARATIONAVIJIT BAKSHI
PRESENTATION CONTAINS THE INFORMATION ABOUT STANDARD OPERATING PROCEDURES FOR PARENTERAL DOSAGE FORM PREPARATION FOLLOWED BY PHARMACEUTICAL MANUFACTURING COMPANIES.
1. Curriculum Vitae
Personal
Saeed Adel El-sayedName
Martial state married
Religion Muslim
Job Chemist
Nationality Egyptian
Age 29 year
Birth day 01/08/1985
Mobile number +966542824113
Address Jeddah
e-mail saeedadel85@yahoo.com
Objective
Seeking a responsible position in your company that is proposed to suit my abilities
With scientific and satisfy my desire to work and self-realization.
certifications
Graduation:
• Bachelor of science, Faculty of science, class chemistry and biochemistry - may 2006
• From Helwan university.
• Grade: very good Percentage: %79.03
Certificate of Course Completion:
• ICDL syllabus version 4 endorsed by ministry of communication and information tech.
• Elementary part 3 certified by education department in sharkia.
• training in water treatment system from NESTLE centre vittel .
• Training in microbiological and chemical analysis from nestle quality
assurance centre vittel.
• Training in 850 professional IC
• Food Safety Principles Training Course in Al Arkkan Training Center for 3 Days
Courses studies
• Analytical chemistry
• Organic chemistry
• inorganic chemistry
• bio chemistry
• Polymers
2. top skills
• HACCP.
• GMP.
• GLP.
• FOOD PROCESSING
Water treatment process.
Desalinated water process.
Soft drink process.
Work Experiences
I worked as chemist in quality & pure company water desalination in Egypt for 2
years.
I worked as water treatment supervisor in Nestlé Waters JEDDAH for 4 years.
Work Description
Analysis of product water (PH - EC- salinity/TDS-O3- CL2- TOTAL ALKALINITY-
TOTAL HARDNESS- TURBIDITY- Ca-Mg-HCO3- SO4- CL—
F- NO3 - NO2- Fe- NH4- MN-
Na- Bro3)
Analysis and monitoring of chemicals use in Bottle Washer (Spearhead Liquid and
H2O2)
Supervision of Water Treatment Plant/Process (Water chlorination, Reverse
Osmosis Operation, Remineralization Process, Ozonation process
Responsible for Nestle Proficiency Test in Chemistry ( ph, EC, BrO3-, NO3-, NO2-
Fe2+, Mn2+, F- ,NH4+)
DO some of Microbiological analysis (TPC, Pseudomonas aeroginusa, Sulfite
Reducing Anaerobic Spores, Yeast and Mould, Coliforms and E.Coli)
Sensory Test Coordinator
Sensorial training coordinator.
Maintaining and implementing the Food Safety Management System (ISO 22000)
Maintaining and implementing the Quality Management System (ISO 9001)
Analysis of Customer Complaints products.
Implementation of GLP and LI’s in the laboratory.
Implementation of GMP and 5’s in the production line and water treatment plant.
Prepare quarterly and yearly samples for external analysis in PTC France.
Responsible for Chemical Storage of the lab.
Responsible for the comprehensive ICP (Internal Control Plan).
Do all water chemical analysis on DR2500, DR2800 spectrophotometer &
NOVA 60 spectroquant.
Instruments Handled:
• Spectrophotometer (HACH DR 2500, HACH DR 2800, MERCK NOVA 60)
• pH meter (Mettler Toledo, HACH SenION3, MYRON pH meter, WTW pH 3210)
• conductometer (Myron USA, HACH sension5, HACH sension EC71)
• Color comparator for chlorine
• Turbidimeter (TURB 355 IR )
• Turbidimeter (TURB 430 IR )
• Autoclave
3. • Incubators
• thermometers
• Digital burettes
• Micro pipette
• Balances (Mettler GB6001-6, Mettler B204-S-phoenix AB-224 )
• Digital caliber
• Ion chromatography(850 professional IC)
Work Experiences in soft drinks
I worked as chemist in Mahmood Saeed Beverage Industry till now.
Work Description in soft drinks
• Chemical analysis
Analysis of finished product (co2 volume - brix -air content – temperature
-weight- titratable acidity - ph)
Collecting reference samples and retention samples and following the chemical
analysis of reference samples during product shelf life time.
Do chemical analysis of boiler water ( chloride - ph - iron - TDS ).
• physical analysis (closure testing)
Removal Torque.
Secure seal test.
• Perform testing
Visual inspection.
Dimensional check
• Bottle testing
Bottle sectional weight.
Bottle wall thickness.
Bottle volume.
Bottle top load
Bottle drop test
Bottle burst test.
Bottle stress crack test.
Bottle thermal stability test.
Carbon Dioxide Retention Testing.
odor and appearance analysis of PET bottles
• Process line
Visual inspection of filtec working in a continuously manner.
Checking the bottle temperature inlet and outlet of warmer.
Control the settings of warmer temperature.
Monitoring date code(production / expiry date) and label of labeller machine.
Monitoring good quality correct label of label machine.
Before loading check code-appearance-correct label of each pallet.
• Microbiological analysis of CSD
4. Do Microbiological analysis (TPC, Yeast and Mould, total Coliforms)
Using sartorius Nutrient pad sets for colony counting by the membrane filter
method.
Instruments Handled in soft drinks:
• Secure seal tester.
• Anton Baar DMA 4500 M.
• Electronic torque tester.
• Mettle Toledo DL22 F& B titrator.
• Branson 3510 (Ultrasonic bath).
• Purelab flex 3 for ultra pure water
• Digital caliber
• Vernier Caliper for bottle height
• Mitutoyo Digimatic Height Gage
• Hot wire bottle cutter
• Digital Top Load tester
• INNOPRO PARAMIX (KHS 2000) TYP CMX 35/T20
• KRONES CONTIMOL MIXER(KRONES AG 2005)