Mohamed Gamal

As a project manager in quality and IT in the pharmaceutical field, I combine in-depth project management expertise with a solid knowledge of the specific regulations of the pharmaceutical industry. My role is to ensure that IT systems and quality processes comply with GxP standards, Good Manufacturing Practices (GMP), and regulatory requirements such as the FDA (21 CFR Part 11).

I oversee the implementation of complex projects, ensuring data integrity, regulatory compliance, and IT system validation. With an approach focused on risk management and quality, I ensure that each project meets the strictest standards, while facilitating technological innovation and continuous improvement of internal processes.

My experience in laboratories and on production lines has allowed me to acquire a solid understanding of quality processes and IT standards in the pharmaceutical sector.

Furthermore, being trilingual, I have been able to manage several projects with different stakeholders from various backgrounds and cultures. I am open to travel to best lead projects.