Driving Quality &
Innovation in Pharma
A dedicated Quality Control Manager and Biotechnology expert with over a decade of experience in world-class pharmaceutical environments.
My professional journey represents a steadfast commitment to patient safety and product excellence. From leading validation protocols at GSK to managing complex QC operations for formulations like Eye Drops, I integrate rigorous scientific standards with strategic operational efficiency.
I specialize in bridging the gap between strict regulatory compliance (cGMP, ICH) and dynamic R&D innovation.
Core Expertise
QC Management
Ensuring product excellence through rigorous testing and compliance oversight. Managing lab operations efficiently.
View DetailsMethod Validation
Developing and validating analytical methods compliant with ICH guidelines. Precision and accuracy guaranteed.
View DetailsCompliance & GxP
Steering operations through complex regulatory landscapes including cGMP, GLP, and ISO 17025 audits.
View DetailsR&D Formulation
Innovation in liquid and eye drop formulations. Bridging the gap between concept and commercial scale-up.
View DetailsTechnical Toolkit
Advanced proficiency in analytical instruments, software, and regulatory standards.
Analytical Techniques
Software & Data
Professional Journey
QC Manager
GenericLab
Leadership in QC operations, ensuring compliance and driving operational excellence across all dosage forms. Implementing new quality workflows.
R&D Manager
PharmAlliance
Spearheaded research initiatives for novel formulations, managing the full lifecycle from bench to pilot scale-up and validation.
QA Responsible
AFROPHARM
Managed QA processes, validation protocols, and regulatory documentation. Oversaw batch release procedures.
QC & Analytical Validation
GlaxoSmithKline (GSK)
Specialized in analytical validation and adherence to global pharmaceutical standards at one of the world's leading companies.
Education
Master's Degree in Biotechnology
USTHB - University of Science and Technology
Snr Technician in Computer Science
Institute of Computer Science
Languages
Resources & Downloads
Analytical Method Validation Protocol (ICH Q2)
PDF • 850 KB
Stability Study Planner Template
XLSX • 1.2 MB
These documents are for demonstration purposes.
Get in Touch
Open for opportunities in Quality Control management and consultancy.