Freelancer profile translated to English.
Back to original languageAbout Elmahdi
Pharmaceutical Quality Control Consultant | Analytical Validation | Regulatory Affairs
With 6 years of experience in the pharmaceutical industry, I support pharmaceutical laboratories in their quality control, analytical method development and validation, analytical transfer, and regulatory compliance projects.
Specializing in chromatographic techniques (HPLC/UPLC) and the requirements of international standards (ICH, USP, European Pharmacopoeia, GMP), I work to ensure the reliability of analytical methods and the compliance of technical files.
French
Native or bilingual
Arabic
Native or bilingual
English
Fluent
Remote only
Primarily works remotely
Experience
- Pharma 5|Analytical Development AnalystMay 2025 - Today (1 year and 3 months)• Analytical method development and validation.• Solubility-Compatibility-Dissolution kinetics studies.• Forced degradation and validation report writing.
- Cooper pharmaQuality Control Laboratory AnalystJuly 2024 - April 2025 (9 months)• Finished product quality control and process validation.Regulatory watch, staff training, audit preparation, and other regulatory activities.
- Pharma 5Quality Control AnalystMarch 2020 - July 2024 (4 years and 4 months)• Raw material, stability, and finished product quality control.• HPLC-GC&UPLC• Infrared, Potentiometry, Kjeldahl, UV-visible, and other analytical techniques.• Report writing, balance calibration, equipment cleaning...
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Education
- Professional Master's in "International Regulatory Affairs for Health ProductsMohammed VI Faculty of Pharmacy2025Mastère Professionnel "Affaires Réglementaires Internationales des Produits de Santé