Odai Samara

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).

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