Ibrahim Shehab
quality r&d director at batterjee pharma cqi irca - qms lead auditor@ Batterjee Pharma
Jeddah, Makkah, Saudi Arabia
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Ibrahim Shehab is a highly experienced Quality/R&D Director with 19 years of expertise in quality control, sampling, packaging materials, raw materials, and microbiology. He has a strong background in R&D, validation, and quality assurance activities. Ibrahim has held various roles in validation, validation, and BE studies, including formulation development for generic pharmaceutical products, Tablet manufacturing techniques, and bioequivalence studies. He is skilled in analytical method validation, root cause analysis, and data integrity. Ibrahim has also worked in the pharmaceutical industry, gaining valuable experience in product development and lifecycle management.
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@batterjee.com
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Quality / R&D Director with 19+ years experience in quality control ( sampling, packaging materials, Raw materials, Finished products, Microbiology ) , R&D (Methodology, Stability studies, Comparative dissolution studies, Bio equivalence studies, New product development), Quality assurance (( Validation, Qualification and Calibration ) activities, IPC, GMP Compliance and QRM).Responsibilities :All Quality control, Quality assurance, R&D and BE Studies activities.Courses :Formulation Development for Generic Pharmaceutical Products.Tablet Manufacturing Techniques.Bioequivalence Studies.Comparative Dissolution Testing & Preparing Biowaiver Reports.Cleaning Validation Towards Complete Compliance.Deviation, Root Cause Analysis (RCA) Tools & Corrective & Preventive Action (CAPA).Auditing.Data Integrity.Data Integrity & Computer System Validation.Qualification.Validation.Validation & Air Conditioning (HVAC) System.Quality Risk Management.Water System.Latest Techniques for Water & Water Waste Analysis.Water Testing Solutions.Good Manufacturing Practices for Pharmaceuticals (GMP).Analytical Method Validation & Development.Validation, Verification & Transfer of Analytical Procedures.Pharmaceutical Stability.Stability Studies & Requirements.Manufacturing & Product Quality.Six Sigma Yellow Belt Course.Compendial HPLC Practice.HPLC Operation, Maintenance & troubleshooting.Basic of HPLC Techniques ,LC Solution & Lab Solution Software.HPLC Concepts.Value Stream Mapping & Waste Identification.BLS course.Chromatography & MS Solutions in Food Safety, Environment, Forensics, Clinical & Toxicology.Design of Stability Studies for Biotechnology Product Development & lifecycle Management.Dissolution Apparatus Qualification: USP Guideline on Procedures for Mechanical Qualification & Performance Verification Test.Drug Dissolution Technology & physical Testing.Active Pharmaceutical Ingredient (API).Final Dosage Forms.Innovative Measuring Solutions.Latest Techniques in Titration & ion Chromatography Instruments.Sanitation & Hygiene.Solutions in Clinical Toxicology & Research.TOC Operation, Maintenance & troubleshooting.Unlock the Value of your Data.

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Work Experience

Phase 4 Industrial City, Jeddah, Makkah, 21443, SA

Pharmaceutical Manufacturing

139

Ibrahim Shehab's Professional Milestones

  • Research And Development Quality Control Director (2012-08-01~): Implementing a comprehensive quality control system to enhance product integrity and enhance customer satisfaction.
  • Manager Quality Control (2012-08-01~2012-08-01): Developed and implemented a comprehensive quality management system, ensuring regulatory compliance and adherence to industry standards.
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