Research & Development

Forensic Toxicology , Equine doping control , Food Safety Analysis , Pharmaceutical Analysis & Environmental Testing. Application development : 1- Analysis of pesticides residues in food and feed by LC-MS-MS , UHR-LC-MS-MS & GC-MS-MS.2-Analysis of Peptide & Protein based drugs in equine urine and blood samples.3- Development of drugs screening and confirmation methods by Q-Exactive UHR , LC-MS-MS & GC-MS-MS in equine blood and urine samples.4-Analysis of PCBs and PAHs in drinking , river & waste water.5-Anaysis of Aflatoxins in Food.6-Analysis of VOCs by Headspace GC-MS.Managing laboratory equipment and facilities :*Thermo Q-Exactive Plus -Accurate mass LC-MS*Thermo TSQ Endura Triple Quad LC-MS.*Thermo ISQ GC-MS FID Headspace injection.*Thermo ICAPQ ICP-MS.*Thermo Flash Protien Analyzer.*Thermo Ion Chromatography. *Agilent GCMSMS.*Agilent GCMS MSD.*DMA Direct Mercury Analyzer.Employing adequate staff Managing and training of junior chemists and technicians.Analytical method development and validation.Analysing test methods with control charts.  Technical validity of results. Compliance of quality checks at different levels. Liaising with the Quality Manager in relation to quality matters affecting testing.Managing R and D projects.

Advising on technical issues faced by the accreditation body during laboratories ISO 17025 audits and assessments .

Forensic Doping control Working on :• Waters UPLC/MS/MS TQD• Bruker maXis 4G LC/MS-QTOF- Accurate Mass• Bruker GC/MS/MS. 320 MS• Bruker Scion TQS• Shimadzu GC/MS-QP 2010 Ultra• Agilent 7890A GC-MS MSD.· Thermo Orbitrap - Exactive Plus - Accurate mass· Thermo TQS-Quantum Ultra LC-MS/MS Screening biological samples for drugs of abuse , performance enhancement drugs and their metabolites. Confirmation of positive findings according to AORC criteria. Training of junior analysts and technicians . Following up maintenance and tuning of the instruments.AORC Professional Member

• Working on HPLC Shimadzu systems ,Mass Spectrometry API 3200 LC/MS/MS and Dissolution apparatus . Pharmacokinetics research ; developing HPLC and LC/MS/MS methods including Plasma extractions, selection of internal standard ,chromatographic parameters for separation and establishing linearity. Method Validation. Determination of C-Max , AUC . Ensuring continuous organized work flow and accurate following of SOPs according to ISO 17025 requirements . Ensuring enough amount of consumables , chemicals , columns to cover the laboratory needs.