i am a Pharmacist/biotechnologist with an extensive knowledge and experiences in molecular biology, Pharmaceutical Biotechnology, Quality Control (qc) of Pharmaceutical products and the development and Validation Analytical methods such as HPLC and gc.
before starting my phd, i had worked as qc Scientist in aburaihan Pharmaceutical company (tehran, iran) for about 3 years. i was scientific and technical expertise in the Quality Control (qc) area. Analysis of active ingredient Pharmaceuticals (api), semi-finished and finished products, development and Validation of Analytical methods, data tracking and record keeping, documented all procedures done in Compliance with gmps and daily calibration of Laboratory instrumentation according to sops were among my main responsibilities.
from january 2014 till october 2014, i have worked as a team Leader of the department of genetic and Biochemistry of a Biomedical Laboratory where i obtained Leadership, management and supervisory experience with outstanding Communication and interpersonal skills. in this role, i supervised a group of five people and i was responsible for mentoring and disciplining of the Lab staff, Training the Lab technicians and assistants on the correct use of Lab equipment and Verification of the test results and report them to the related authorities.
as my resume shows, i have profound knowledge and work experience in molecular biology and Pharmaceutical Biotechnology, i am skillful in qc of Pharmaceutical compounds and operation, development and Validation of several Analytical methods such as GC-MS, HPLC, ft-ir spectrometry, NMR, UV-Vis, ELISA, (q)rt-PCR, Western blot and more other. besides, i am well educated in ICH guidelines, cGMP and glp, and i am familiar with compendia methods such as us, european/british pharmacopeias and national formulary (nf).
i am fluent in writing and speaking in English and i can communicate in French and i have a basic knowledge of dutch. i am a good team player who enjoys working as a team Member as well as independently.
Lab manager Shiraz, Fars, IranJanuary 2014 --- December 2014
Research Scientist Ghent, BelgiumJanuary 2009 --- June 2013
Quality control scientist Tehran, IranMay 2006 --- December 2008
Pharmacy manager Shiraz, Fars, IranApril 2004 --- March 2006
Attention to detailProactivityOrganizationInterest in knowledgeFlexibilityCuriosityCreative thinkingCompetitivenessCollaborationAdaptabilitySociability
In VitroResearch GovernanceDrug metabolismSearch literature on clinical trialsWestern BlottingDrug InteractionWriting Study Procedures and SOPsPharmacyChemistryPharmacodynamicsCell CulturePharmaceutical IndustryBiotechnologyPCRBiopharmaceuticalsNew Drug Application (NDA)BioinformaticsNegotiationBiomarkersMolecular CloningBiological Drug Developmentmolecular biologyBioavailabilityMolecular & Cellular Biology Scientific writingMicrosoft Office R&DMicrosoft ExcelDrug development processMicroscopyELISAPowerPointEnglishPre-clinical researchImmunoprecipitationQuantitative PCR (qPCR)ImmunofluorescenceVerificationICH-GCPValidationICH GCP guidelinesUnderstand levels of research evidenceHPLCUnderstand how results translate to practiceGood Manufacturing Practice (GMP)TransfectionGood Clinical Practice (GCP)Technical reportsGMPTeam LeadershipGood Laboratory Practice (GLP)SOPGCPScientific WritingFluorescence MicroscopyScientific methodologyEnzyme-linked immunosorbent assay (ELISA)RT-PCR BiochemistryR&DKnowledge of the drug development processLaboratoryActions and modes of action of drugs in the human speciesInfectious diseasesBiochemistryIn VitroCMC Drug metabolismData AnalysisDrug InteractionDNA extractionChemistryDrug safety assessmentCell CultureDrug substance developmentBiotechnologyDNABiopharmaceuticalsFDABioinformaticsFluorescent microscopyBiomarkersGeneticsBiological Drug DevelopmentLaboratory study designBioavailabilityMedical writing Scientific writingpeople management R&DPharmacokineticsDrug development processpharmacologyELISAProtein ExpressionEnglishProtocolImmunoprecipitationProject ManagementImmunofluorescenceResearch GovernanceICH-GCPSearch literature on clinical trialsICH GCP guidelinesWriting Study Procedures and SOPsHPLCGood Manufacturing Practice (GMP)Good Clinical Practice (GCP)GMPGood Laboratory Practice (GLP)GCPFluorescence MicroscopyEnzyme-linked immunosorbent assay (ELISA) BiochemistryKnowledge of the drug development processActions and modes of action of drugs in the human speciesBiochemistryCMC Data AnalysisDNA extractionDrug safety assessmentDrug substance developmentDNAFDAFluorescent microscopyGeneticsLaboratory study designMedical writingpeople managementPharmacokineticspharmacologyProtein ExpressionProtocolProject ManagementResearch GovernanceSearch literature on clinical trialsWriting Study Procedures and SOPs
Skills and Expertise
life sciencebiotechnologymolecular biology pharmaceutical sciences
Ph.D. in Biotechnology from Ghent university in 2013
Advanced Master in Pharmaceutical Sciences from Shiraz University of Medical Sciences and Health services in 2006