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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.

i earned my degree in Pharmacy in 2006 and i have earned my phd in Biotechnology in 2013 from ghent University (ghent, belgium).

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. 


Past Experience

  • Lab manager Shiraz, Fars, Iran

    January 2014 --- December 2014

  • Research Scientist Ghent, Belgium

    January 2009 --- June 2013

  • Quality control scientist Tehran, Iran

    May 2006 --- December 2008

  • Pharmacy manager Shiraz, Fars, Iran

    April 2004 --- March 2006


Self Assessment :
Attention to detailProactivityOrganizationInterest in knowledgeFlexibilityCuriosityCreative thinkingCompetitivenessCollaborationAdaptabilitySociability


Self Assessment :
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

Self Assessment :
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


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Notice Period:
    2 weeks
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position
    BrightOwl employee
  • International:

Area / Region

Ghent, Belgium


Driving License
  • Yes

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