Dr. Lydia Eshak
QUALITY ASSURANCE / REGULATORY AFFAIRS SPECIALIST
MSc in MBA (Strategic Planning), Bachelor Degree in PharmacyAbout Me:
I am a highly dedicated and meticulous Quality Assurance and Regulatory Affairs Specialist with a robust background in clinical pharmacy, regulatory compliance, and quality assurance. My experience spans over several years in managing regulatory affairs, ensuring compliance with industry standards, and improving the quality of healthcare services. My expertise in project management, drug development, and complex problem-solving equips me with the skills necessary to excel in high-pressure environments. I am committed to maintaining the highest standards of medical ethics and regulatory compliance, driving continuous improvement in clinical and regulatory practices.
Education:
| Year | Degree | Institute |
|---|---|---|
| 2017-2019 | Master of Business Administration - MBA, Strategic management - Grade: Excellent with honor, Rank: 1st in class | Arab Academy for Science, Technology and Maritime Transport |
| 2007-2012 | Bachelor of Pharmacy - BPharm, Pharmacy - Grade: Excellent with honor | Ahram Canadian University - ACU |
QUALITY ASSURANCE / REGULATORY AFFAIRS SPECIALIST
| Year | Department | Position | Hospital |
|---|---|---|---|
| 2024 | Quality Assurance / Regulatory Affairs Specialist | Cliniquest Research Site | |
| 2019-2024 | Pharmacy Store Procurement Manager | Coptic Mission Hospital | |
| 2013-2019 | Regulatory Affairs Specialist | Egyptian Drug Authority (EDA) |
Appointmnet Schedules:
| Day | Time | |
|---|---|---|
| Sun | 8:00am - 1:30pm | Appointment |
| Mon | 11:30am - 2:30am | Appointment |
| Thu | 12:30am - 2:30am | Appointment |
I am a highly dedicated and meticulous Quality Assurance and Regulatory Affairs Specialist with a robust background in clinical pharmacy, regulatory compliance, and quality assurance. My experience spans over several years in managing regulatory affairs, ensuring compliance with industry standards, and improving the quality of healthcare services. My expertise in project management, drug development, and complex problem-solving equips me with the skills necessary to excel in high-pressure environments. I am committed to maintaining the highest standards of medical ethics and regulatory compliance, driving continuous improvement in clinical and regulatory practices.
CERTIFICATIONS
- Evaluation of Clinical Trials
- Anti-Microbial Resistance Certificate
- Common Technical Documentation (CTD)
- New Trends and Basics of Clinical Pharmacy
- ITP-GCP Transcelerate Equivalent Modules, Statistical Analysis-Audit Inspection Readiness