QA Engineer

• Sep 2021 - Present

-As a key member of an agile team, I structurally improve and validate the overall product quality with a focus on mindset, test activities, environments, coaching, and automation. Fully responsible for the quality of the document delivery and document stability. -Actively involved in the entire QA process, from design to development, testing, and release into production to guarantee the right quality. -Testing the complete process flow (document, different scenarios, e-invoice, archiving...) of the document. -Preparation, revision, protection, distribution of all SOP's in the Quality Management System. -Preparation, revision, protection, distribution of "how-to-validate" documents to improve the validation process and spread the knowledge among all businesses.

IT QA Engineer

• Sep 2021 - Present

-As a key member of an agile team, I structurally improve and validate the overall product quality with a focus on mindset, test activities, environments, coaching, and automation. Fully responsible for the quality of the document delivery and document stability. -Actively involved in the entire QA process, from design to development, testing, and release into production to guarantee the right quality. -Testing the complete process flow (document, different scenarios, e-invoice, archiving...) of the document. -Preparation, revision, protection, distribution of all SOP's in the Quality Management System. -Preparation, revision, protection, distribution of "how-to-validate" documents to improve the validation process and spread the knowledge among all businesses.

Quality Assurance Coordinator

• Jan 2021 - Sep 2021

- Monitor all activities, processes, and procedures of the Quality team.- Preparation, revision, protection, distribution of all SOP's in the Quality Management System.- Define the standards of the expected product quality for the team allowing them to identify, prevent and treat nonconformity in alignment with the customers quality policies.- Responsible for internal and external incidents or nonconformity detected by the Quality team. Make necessary analysis to deeply investigate complaints within the predefined time-range. Examine root causes and conclude findings to upper management. - Ensure all quality management systems implemented in the warehouse are in line with ISO 9001 requirements.- Responsible for regulatory changes according to the ISO 13485 Medical Devices with a correct application and awareness throughout the organization.- Manage the block-release requests of the customer and perform accordingly. - Initiate and follow regulatory corrective and preventive actions (CAPA) to eliminate nonconformity detected during the internal and external audit.-Set KPIs and the measurements. -Plan and execute WMS Validation-Prepare training programs and training materials per each task with their qualification methods.-Organize and lead the training sessions.-Plan Internal Audits and Self-Inspection Program with their CAPA and Investigation methods.

Inventory Control Specialist and SAP Key User

• Mar 2019 - Jan 2021

-Controls inbound, outbound and internal warehouse stock movements. -By applying the standard procedure for over-under delivery, ensures the necessary correction and organizes the declaration of this to the sender.-Investigates WMS-related issues and takes necessary actions to prevent re-occurrences. -Examines the errors in stock entry and exit documents and works in coordination with the IT department for systemic correction.-Making year-end stock profit-loss study and declares it to the management.-Organizes monthly/yearly stock count. -Creates necessary reports on stock and organizes it to their distribution among customer management,-Ensures that all inventory control activities inside and outside the operation are organized.

Research Assistant

• Jan 2017 - Sep 2017

Volunteer

• Jun 2012 - Jun 2015

Summer Intern

• Jul 2013 - Sep 2013