Ahmad sarakbi
Senior Research And Development Scientist @ invoX
About
Senior R&D Scientist with 20+ years of experience in analytical chemistry across academia and industry, spanning pharmaceutical development, medical devices, and inhalation products.I involved in the analytical activities for Soft Mist Inhaler (SMI) development, including analytical method development, validation, and transfer in GMP/GLP environments. My role includes leading and overseeing analytical work performed by external GMP partners (CROs), ensuring scientific robustness, data integrity, and compliance with ICH Q2, EP, USP, ISO 13485, and FDA expectations.I have strong experience in defining and leading validation strategies, reviewing GMP data packages generated by partners, managing deviations and OOS/OOT investigations, and contributing to regulatory‑ready documentation and Quality Management Systems.Technical focus: HPLC/UPLC, NGI, Spraytec, Mass Spectrometry (QDM), Empower, JMP, analytical validation, and GMP partner oversight.
Belgium
Brussels
Pharmaceuticals
Analytical Skills, SAP Environment, Health, and Safety Management (EHS), Troubleshooting, Defining Requirements, Research and Development (R&D), University Teaching, Research, French, Arabic, English, Electrochemistry, Liquide chromatography, UV/Vis, Atomic Absorption, Chemistry, Physics, Teacher-assistant in different universities, Supervisor in differents laboratories for undergraduated stuents, Analytical Chemistry, High-Performance Liquid Chromatography (HPLC), Science, Analytical Method Validation
Experience

Senior Scientist
Belgium
• Development of analytical methods received from clients (improve the separation –selectivity, capacity, efficiency…etc.-, and LOQ • Routine work: Check the quality of API, intermediate and raw materials used in (ex: methanol as raw and intermediate material) • Participate in writing protocols for qualification (pre-validation) of HPLC/UPLC/Uv-Vis to check the method criteria (LOD, LOQ, range) • Writing SOP for validation, then execute experimental work as defined in the protocol • Reporting and presenting results • Transfer method to between departments • Follow up the stability • Participate in the laboratory quality system activities such as internal audits, writing standard operating procedures, and documentation review • Driving the deviation • Ensure compliance with company policies and SOPs as well as FDA and GMP guidelines • Ensure compliance with the validation of analytical procedures guideline ICH Q2 (R1) and GLP • HPLC, UPLC, , Uv-Vis, IR, GMP, GLP, ICH Q2 R1

Scientific Collaborator
Brussels Area, Belgium
Scientific collaborator: Faculty of pharmacy, ULB, Belgium • Improvement of an (HPLC/electrochemical detector) analytical method for the determination of amino-thiol molecules in order to widen the applicability of the method in more complex medium (brain) • Review scientific papers (intra-department) in order to publish them in journals • Reviewer at Talanta international journal for judging the work of researcher who would to publish their work in the journal • HPLC, UPLC, Electrochemistry, Uv-Vis, IR)

Visiting Researcher
Brussels Area, Belgium
• Supporting researches • Coordinating analytical method development activities • Development methods for small molecules (amino-thiols) and some heavy metals according • HPLC, UPLC, Uv-Vis, IR, Electrochemistry

Internship
VUB

Professor Assistant
Aleppo University
• Research and Lab teaching ; Analytical chemistry, Organic, Inorganic chemistry, and Biological chemistry • Liquid chromatography, Uv-Vis, Potentiometry, Electrochemical analysis, Quantitative and quantitative techniques • Lab manager of analytical chemistry

QC Chemist
AECS

Professor Assistant
AlBaath university
Homs, Syria
• Research and Lab teaching; Organic chemistry, General chemisty and Instrumental analytical chemistry • Liquid chromatography, Uv-Vis, Potentiometry, electrochemical anaysis, atomic absorption, flame emission spectroscopy • Lab manager of analytical chemistry
Education

Pharmaceutical and biomedical sciences
Development a new electrochemical methods for the analysis of pharmaceutical molecules such as Biothiols as Cysteine, Glutathione, and Homocysteine, Acetaminophen, Ascorbic acid....etc. New methods using different electrochemical detectors such as silver and screen printed electrodes, the detectors were coupled with a chromatographic system. Different columns were used such as aninic, cationic, C18, and C8. Classic and monolithic. Title " Contribution of the development of electrochemical methods for liquid chromatographic analysis and drug quality monitoring "
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