

Quality Control Specialist with proven experience in pharmaceutical quality systems and regulatory compliance. Skilled in implementing and maintaining quality standards including ISO requirements and Good Manufacturing Practices (GMP). Experienced in documentation control, Good Documentation Practices (GDP), and supporting deviation handling and continuous improvement processes. Actively contributed to regulatory processes, including coordination and documentation preparation for Saudi Food & Drug Authority (SFDA) accreditation.
(Commercial Drug Warehouse) | 2022 – 2025
• Managed pharmaceutical operations including procurement coordination and client interactions within healthcare sector
• Ensured compliance with pharmaceutical quality standards across procurement and distribution processes
• Reviewed product specifications and verified alignment with regulatory and quality requirements
• Managed documentation in accordance with Good Documentation Practices (GDP)
• Monitored product quality, identified deviations, and reported discrepancies for corrective action
• Participated in supplier evaluation and product acceptance processes
• Supported implementation of quality procedures while maintaining daily operational responsibilities
• Collaborated with internal teams to ensure alignment between business operations and quality standardsregulatory expectations and quality standards
• Maintained excellent relationships with procurement departments across assigned hospitals
• Conducted scientific presentations for physicians and healthcare professionals on drug mechanisms of action, proper usage, dosage, and safety profiles
• Provided detailed explanations of adverse effects and ensured safe and effective product use
• Reported observations and potential issues to internal teams to support product monitoring and continuous improvement
• Achieved 146% of sales target in the first year
Good Documentation Practices (GDP)
Regulatory Compliance & Quality Standards
Deviation Handling & Root Cause Analysis
CAPA (Corrective and Preventive Actions)
SOP Implementation & Process Standardization
Audit Support & Quality Inspection
Documentation Review & Quality Reporting
HPLC-UV Method Development & Validation
Analytical Method Validation & Verification
Instrumentation: HPLC, GC, FTIR, UV-Vis Spectroscopy
Data Analysis & Interpretation of Analytical Results
Quality Control Testing & Laboratory Procedures
• Pharmaceutical Good Manufacturing Practice (GMP) Training
• ISO 9001:2015 Internal Auditor Certification
• ISO 17025: Laboratory Quality Management Systems
• Quality Assurance in Pharmaceuticals
• CAPA & Deviation Management
• Good Documentation Practices (GDP)