Biography

About the Instructor

Dr. Yomna Ahmed Adel Mohammed is an accomplished Industrial Pharmacy professional and Ph.D. holder, with extensive experience bridging pharmaceutical research, quality management, and regulatory compliance. She has worked across R&D, reference laboratories, and quality assurance roles, specializing in pharmaceutical development, GLP/GMP inspections, ISO 17025 auditing, stability studies, and regulatory project management.

Dr. Yomna is recognized for her ability to translate complex scientific concepts into practical, industry-ready skills. Her experience in both Egyptian regulatory authorities and pharmaceutical manufacturing environments gives her learners unique insights into real-world quality, compliance, and analytical practices.

At PharmaCores, Dr. Yomna’s courses focus on practical pharmaceutical R&D, quality management, and regulatory strategies, equipping learners with the tools, methodologies, and confidence needed to excel in industrial and regulatory pharmacy roles.

---

Education

• Ph.D. in Industrial Pharmacy – Faculty of Pharmacy, Cairo University, Egypt (2024)

• M.Sc. in Industrial Pharmacy – Faculty of Pharmacy, Cairo University, Egypt (2022)

• B.Sc. in Pharmaceutical Sciences – Faculty of Pharmacy, Cairo University, Egypt (2016), Very Good

Professional Qualifications

• Total Quality Management (TQM) Diploma – American University in Cairo (2018)

• Certified Six Sigma Black Belt – IQF (2022)

• ISO 9001:2015 Lead Auditor – IRCA (2023)

---

Professional Experience

• Senior International Cooperation Coordinator – Chairman Office, Egyptian Drug Authority (EDA)

• Technical Bureau Member & Project Manager – WHO PQ Labs & CRO Projects, EDA

• GLP Inspector & Quality Assurance Specialist – EDA, WHO GBT Project

• Quality Control Specialist – NODCAR & Evapharma

• Community & Training Roles – Various pharmacies and pharmaceutical companies, including Janssen, Vacsera, and Sultan Pharmacy

---

Areas of Expertise

• Pharmaceutical R&D & Industrial Pharmacy Practices

• Quality Management Systems (ISO 9001, ISO 17025) & GLP/GMP Compliance

• Stability Studies, Analytical Evaluation & HPLC Troubleshooting

• Regulatory Project Management & CRO/WHO PQ Projects

• Staff Training, Mentoring & Scientific Workshops

• Risk Assessment, Documentation & Quality Assurance

---

Academic & Industry Contributions

• Conducted workshops and training for postgraduate students and industry staff on Six Sigma, Quality Management, and Regulatory Compliance

• Managed WHO prequalification laboratory projects and CRO projects within EDA

• Published peer-reviewed research articles on transdermal and intranasal drug delivery systems

• Actively contributed to the development of quality assurance protocols, audits, and analytical standards in Egyptian pharmaceutical operations

Courses