Quality Officer – Tissue & Hygienic Paper Manufacturing at Fine Hygienic Holding (2025-01 – Present)
- Monitoring production lines to ensure compliance with product specifications, GMP, and hygiene standards.
- Inspecting in-process materials and addressing deviations with production teams.
- Verifying machine settings and product attributes (strength, softness, absorption, dimensions).
- Conducting physical tests on tissue products (tensile strength, softness, absorption, grammage, thickness).
- Testing raw materials and verifying compliance with acceptance criteria.
- Recording and validating test results; ensuring equipment calibration and accuracy.
Quality Assurance Supervisor at lamis Detergents Co. (2024-01 – 2025-12)
Quality Assurance Supervisor in Detergents & Cosmetics Industry
- Implementing and maintaining QA systems to ensure full compliance with GMP, ISO 9001.
- Overseeing production operations to verify adherence to quality specifications and hygiene controls.
- Reviewing and approving batch records, COAs, and product release documentation.
- Conducting internal audits and leading corrective & preventive actions (CAPA).
- Coordinating with Production, R&D, and QC to resolve non-conformities and improve process performance.
- Managing all quality documentation and ensuring regulatory compliance.
- Supervising testing of raw materials, in-process samples, and finished products.
- Validating and verifying analytical and physical test methods.
- Ensuring calibration, maintenance, and proper function of laboratory instruments.
- Reviewing test results and authorizing product release based on specifications.
- Training laboratory staff on testing protocols, data integrity, and quality procedures.
Qualite Assurance IPC and GMP at Dar Aldawa pharmaceutical industries (2023-01 – 2024-12)
For Liquids and semi solid
- Ensured full compliance with GMP requirements throughout manufacturing processes.
- Conducted in-process quality checks for liquids, creams, and suppositories to ensure adherence to approved specifications.
- Reviewed and verified batch manufacturing records (BMR) for accuracy and completeness.
- Monitored critical process parameters and ensured consistency in production quality.
- Performed line clearance and ensured proper cleaning and sanitation procedures.
- Identified, documented, and reported deviations, and supported investigation processes.
- Collaborated with Production and QC teams to resolve quality issues and implement corrective actions (CAPA).
- Ensured proper documentation practices in line with regulatory and internal quality systems.
- Supported continuous improvement initiatives to enhance product quality and process efficiency.
senior Quality control Analyst at Itqan pharmaceutical industries (2020-01 – 2023-12)
- Practical training was conducted on laboratory instruments, including HPLC, UV, and IR, with a focus on understanding how each device works and its various applications.
- Report any problems or devotion or OOS and Quality Team.
- Prepare Working Standard.
- Receiving standard materials, whether from Edqm or USp or other private companies, entering them into the system and making consumption sheet.
- Communicating with warehouse employees, coordinating notifications of the arrival of raw materials or packaging materials, printing special labels and managing materials on logbook Receving.
- Preparation of Molar and Normal Volumetric Solutions Liquid and Solid.
- Carrying out chemical and physical tests (Assay, Related manual titration, water content, IR, loss on drying, loss on ignition, melting point, Sulphate Ash, SOR and other test in USP & EP).
- Water Analysis: (TOC, Nitrate, PH, Cond, Chlorine hardness, TDS).
Quality control analyst at UNITED Pharmaceutical Company (2017-01 – 2019-12)
- Analysis of active and inactive raw materials.
- Carrying out chemical and physical tests: Assay, Related, manual titration, water content, IR, Loss on drying, loss on ignition, melting point, Sulphate Ash, SOR and other test in USP & EP.
QA (IPC) Packaging at TQ PHARMA Company (2016-01 – 2017-12)
Performing all required tested for Raw Material and Finished products 'all forms'
- Practical training was conducted on laboratory instruments, including HPLC, UV, and IR, with a focus on understanding how each device works and its various applications.
- Report any problems or devotion or OOS and Quality Team.
- Prepare Working Standard.
- Receiving standard materials, whether from Edqm or USp or other private companies, entering them into the system and making consumption sheet.
- Communicating with warehouse employees, coordinating notifications of the arrival of raw materials or packaging materials, printing special labels and managing materials on logbook Receving.
- Preparation of Molar and Normal Volumetric Solutions Liquid and Solid.
- Carrying out chemical and physical tests (Assay, Related manual titration, water content, IR, loss on drying, loss on ignition, melting point, Sulphate Ash, SOR and other test in USP & EP).
- Water Analysis: (TOC, Nitrate, PH, Cond, Chlorine hardness, TDS).
