Meet the founder behind MENA MedTech and learn about the leadership approach that connects technical quality with dependable project execution.
I bring 15 years of experience across medical device and pharmaceutical environments, with work spanning R&D, quality, manufacturing engineering, design controls, regulatory documentation, and post-market activities.
In addition to my technical background, I am a people manager and CEO-minded business leader. I have managed teams of 50+ people, coordinated cross-functional stakeholders, and focused on executing and delivering projects on time.
My experience also includes traveling with Marketing teams to recruit and engage surgeons for product demonstrations, collect voice-of-customer feedback, and translate clinical workflow needs into product redesign inputs. I use Power BI to build performance dashboards and track device and project metrics, supporting data-informed decisions.
Healthcare service experience across the Kingdom, combining medical-device lifecycle analysis with operational metrics and live Power BI reporting.
Healthcare-sector project experience associated with the Ministry of Health in Riyadh. Visit the official Ministry of Health website for information about the organization and its services.
Official Ministry of Health website ↗Completed services supporting hospitals in AlUla, Riyadh, Madinah, Makkah, Jeddah, and Tabuk.
Analyzed medical devices and connected device data to performance metrics designed to track lifecycle status, utilization, service needs, and failure events. Reported these indicators through live-data Power BI dashboards to help stakeholders monitor device performance, identify trends, and support maintenance and replacement decisions.
Learn about Power BI ↗Organization names and links are provided for professional experience context only and do not imply endorsement or current affiliation. Dashboard wording describes project experience and does not expose confidential hospital or device data.
Select any tool below to open its official website or product overview in a new tab and learn what it does.
Business intelligence dashboards and reports for monitoring performance and trends.
Official website / overview ↗Electronic quality management for medical-device software and regulated product development, including controlled documentation, traceability, and quality workflows.
Official website / overview ↗Electronic Quality Management System software for managing quality processes and records.
Official website / overview ↗Electronic Document Management System for controlled documents, approvals, and revisions.
Official website / overview ↗Life-sciences quality and document applications supporting regulated workflows.
Official website / overview ↗Software that tracks and manages production activity on the manufacturing floor.
Official website / overview ↗Enterprise Resource Planning software that connects business operations such as purchasing, inventory, finance, and production.
Official website / overview ↗Quality and CAPA management software supporting corrective actions, investigations, approvals, and quality-compliance workflows.
Official website / overview ↗Quality management software for nonconformances, CAPA, audits, and compliance workflows.
Official website / overview ↗A language used to query, analyze, and manage data in relational databases.
Official website / overview ↗Spreadsheets for analysis, calculations, tracking, and reporting.
Official website / overview ↗Document creation and review for reports, procedures, and technical documentation.
Official website / overview ↗Presentation software for project updates, reviews, and stakeholder communication.
Official website / overview ↗Digital notebooks for meeting notes, task capture, and reference material.
Official website / overview ↗A programming language used to automate work and analyze data.
Official website / overview ↗Statistical analysis software used for quality improvement and process studies.
Official website / overview ↗CAD/CAM/CAE software for product design, engineering, and manufacturing.
Official website / overview ↗3D CAD software for mechanical design and product development.
Official website / overview ↗Product lifecycle management (PLM) for product data, change, and configuration management.
Official website / overview ↗3D CAD and product design software; Creo is the successor product family to Pro/ENGINEER.
Official website / overview ↗Engineering simulation tools used to evaluate product performance and design.
Official website / overview ↗Computational fluid dynamics software for modeling fluid flow and heat transfer.
Official website / overview ↗21 CFR Part 820 is the FDA Quality Management System Regulation (QMSR) for medical-device quality systems. Effective February 2, 2026, the QMSR incorporates ISO 13485:2016 by reference and includes FDA-specific requirements. It applies to finished-device manufacturers within its scope.
FDA QMSR overview & requirements ↗FDA database: 21 CFR Part 820 ↗My experience spans projects in medical device and pharmaceutical environments. Explore the official company websites and product portfolios below. These links are provided for context and do not imply endorsement or current affiliation.
Note: 3M’s former healthcare business operates as Solventum; the product link directs to Solventum’s official site. Please confirm whether “IPG” refers to IPG Photonics before publishing if you meant a different organization.
From a project charter to design transfer and post-market support, I help teams establish clear plans and workable deliverables.
Project charters, development plans, scope, milestones, and ownership.
Design controls, engineering coordination, manufacturing readiness, and transfer.
Risk files, CAPA/NCR, audit readiness, technical documentation, and remediation.