fatima ezzahra samkouk

I managed a team of 30+ Quality Analysts, driving a 10% increase in productivity through cross-location projects. By surpassing SLAs by 6%, I ensured exceptional service delivery. My collaboration with stakeholders facilitated successful implementation of Global/EMEA Frameworks, while my expertise in web-based tools enabled insightful problem-solving strategies. I also streamlined operations through efficient workload forecasting and real-time resource management.

In my mission to ensure the production and availability of PQ Facilities deliverables for the GlaxoSmithKline (GSK) project, I prepared comprehensive facility validation summaries, maintaining a 0% overturn rate. Additionally, I reported and resolved non-conformities, leading root cause analysis and CAPA efforts. Serving as a spokesperson for GSK, I facilitated effective communication and goal alignment between the client and the team

In my mission to contribute to the deployment of HSE standards and risk prevention, I conducted thorough prevention tours, maintaining compliance with safety regulations. I successfully implemented a Risk prevention system, resulting in a significant 20% reduction in incidents in 2019. Additionally, I led a comprehensive safety culture diagnosis, utilizing data-driven methods to enhance safety awareness training and designing user-friendly HSE forms and posters to promote safety guidelines

In my role, I have been dedicated to implementing enhancement strategies and effectively executing CAPA plans, ensuring continuous improvements in our processes. I have actively contributed to our preventive measures, consistently identifying and mitigating potential risks before they escalate. I established and meticulously maintained measurement control charts for tracking key quality parameters, allowing for real-time quality control and ensuring optimal product performance

As part of the ISO 22000 implementation at the KNORR factory, I provided comprehensive training to operators, boosting engagement by 15%. I conducted weekly GMP inspections, leading to a 25% improvement in adherence to quality standards. Additionally, I organized and maintained audit binders, achieving a 100% audit readiness score, and effectively managed micro testing, resulting in a 15% reduction in product contamination incidents.

I implemented robust traceability procedures, ensuring accurate documentation of all operations. Additionally, I conducted comprehensive verification of critical parameters, maintaining stringent product quality standards. Proficient in precise physicochemical analyses, I assessed sample composition and characteristics. Moreover, I interpreted analysis results to diagnose non-conformities, implementing effective corrective actions to uphold product integrity

I conducted quality checks on laboratory reagents to guarantee precise analysis results. Additionally, I demonstrated proficiency in preparing accurate chemical solutions tailored to specific analytical procedure requirements. Furthermore, I conducted comprehensive medical analyses, including bacteriology, biochemistry, and hematology, adhering strictly to established protocols and guidelines.