*Quality monitoring * Customer Complaints * CAPA preparation * New vendor Audit and approval* FSSC audit, ISO audit, GMP audit and customer audit.* New product Development

• Implementing and Practices of TQM (Total Quality Management system)• Ensuring the GLP and GMP in every step of the Quality Control and Production floor.• Collaborating with production teams to rectify production and maintain high-quality final products.• Implementing ISO 9001 2015 (QMS)• Expanding cross-functional organizational capacity by collaborating across departments on priorities, functions and common goals.• Supervising production workers to identify areas in need of improvement for high-quality production• Inspecting and packaging products meticulously according to malfunctioning specifications.• Conducting Quality Guideline training to employees (ISO, GRS, FSSC, US-FDA guideline, GMP, GLP, Good Documentation Practices, SOP, Protocol, Manual, ISO implementations, Chemical Handling procedure).• Analyzing any chemical products (Food and Beverages, Drugs, Plastic, Cosmetics, Oil, Chemical Plant product, Packaging materials).Key Achievements: • Maintained and monitored 19 team members and conducted 30 to 35 training yearly.• Implemented ISO, GRS, EFSA (EU), and FSSC certifications.• Reduced laboratory costs by 26% yearly.• Implemented and invented new laboratory types of machinery and analytical process. • Developed 64 new SOP for all kinds of quality, production and warehouse.

• Analyzed products and oversaw the product development process to ensure that products meet quality standards.• Handling a variety of Quality Control instruments, such as GC, HPCL, NIR, UV, FTIR, IV & AA-Analyzer.• Conducted Out-of-Specification (OOS), Out-of-Trend (OOT), Limit of Instrumental Recovery (LIR), and deviation analysis for raw and finished goods, packaging materials, and water analysis.• Ensured Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP) and Six Sigma methodologies are maintained throughout production and laboratory processes.• Developed and implemented quality control and assurance processes to ensure product.• Conducted regular inspections & tests to ensure that products and services meet established standards.• Oversee the creation and maintenance of quality records, such as inspection reports and test results.• Collaborated with other departments (such as product development and production, IT) to ensure that quality standards are integrated into all product development and production processes.• Developed and conducted quality training programs for employees to ensure they understood and adhered to established quality standards.• Conducted root cause analysis to identify the source of quality problems and implement corrective action to prevent reoccurrence.• Ensured products and services complied with relevant regulations and standards US-FDA, WHO, UK-MHRA, and KSA.• Staying up-to-date with the latest quality control and assurance methodologies and technologies.• Monitored quality performance & implemented improvement initiatives to drive quality excellence.• Representing the company in external quality-related audits and assessments.Key Achievements:• Developed R&D work, method validation, process validation, and cleaning validation.