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Experiences

Past Experience

  • Pharmacist, Analytical Scientist, PhD Candidate Ghent, Belgium

    October 2012 --- September 2016

    currently i am pursuing my doctoral thesis at the drug quality and registration (druquar) Laboratory of the faculty of Pharmaceutical Sciences, ghent University, belgium. druquar, a medicines Quality Control Laboratory, is one out of only two belgium University labs with a current accredited GMP license. at druquar, fundamental and applied Research is carried out in the fields of pharmaceutical Analytics and Regulatory Affairs, with our general Research goal being the study of the functional quality of Pharmaceuticals and related products. besides my own Research, i am head responsible for the implementation of the Quality System and Quality Assurance of our Lab. moreover, as a University Member, i also contribute to the Education of Pharmaceutical Sciences students by giving practical sessions and supervising thesis students. druquar, under the lead of mentor/promotor prof. bart de spiegeleer, creates a unique learning environment for phd students, as we are not only focussing on our own Research but we are also in close contact with the Pharmaceutical Industry and government, since we are performing contract services such as Quality Control analyses for the belgium federal agency for medicines and Health products, as well as Consulting services regarding analytical method development and Validation.

  • Interim Pharmacist Aalst, Kruishoutem, Oudenaarde, Eeklo

    July 2012 --- August 2012

    during the summer of 2012 (directly after obtaining my masters degree in Pharmaceutical Sciences and before starting my phd) i worked in four different pharmacies (located in: aalst, kruishoutem, oudenaarde and eeklo) all owned by ‘de lindeboom apotheken’. i was either working together with other Pharmacists or i was the sole responsible Pharmacist, working alone or together with pharmaceutical technical assistants. giving Pharmaceutical Care and managing prescriptions and orders. since i switched a lot between different pharmacies (i was Interim/replacing Pharmacist) during a very short time span, fast adaption to a new environment was a quality highly appreciated by my superiors and by the patients as well.

  • Order Picker Kruishoutem, Belgium

    July 2007 --- August 2010

    during the summer holidays of my Higher Education studies i was an order picker at belspeed, a clothing distribution company.

  • Waitress Kruishoutem, Belgium

    January 2005 --- December 2007

    during my secondary education i was a Waitress in the weekends.  i quit this weekend job because it was difficult to combine with my Higher Education studies.

  • Playground supervisor Kruishoutem, Belgium

    July 2005 --- July 2005

    during the summer of 2005 i was a playground Supervisor/monitor. it was my responsibility to take care of children (3 to 14 years old) while their parents were working. we organised i.a. games, activities and excursions (from 8h to 18h).

Personality

Self Assessment :
AdaptabilityAnalytical thinkingAttention to detailAssertivenessCharmCommunicativeCritical thinkingCoordinationCuriosityDominanceEfficiencyFlexibilityIndependenceInterest in knowledgeOrganizationProblem solvingProactivityResiliencyResponsibilityResult OrientedSelf-confidenceSelf-disciplineSociabilityTrust

Knowledge

Self Assessment :
R&D Labtechnician Scientific writingActions and modes of action of drugs in the human speciesAnalysisAnalytical ChemistryAnalytical Method ValidationAnalytical methodsAnalytical proceduresAnalytical techniquesAnimal ModelsAssay developmentAuditingBioanalysisBiological Drug DevelopmentcGMPChromatographyCMC Regulatory AffairsCommunication SkillsCurrent Good Manufacturing Practice (CGMP)Data AnalysisData entryData ManagementDermatologyDrug DevelopmentDrug regulatory authoritiesDrug metabolismDrug substanceseCTDEnglishGalenicsgas chromatographyGMPGood Manufacturing Practice (GMP)Grant PreparationGrant WritingGraphPad PrismHospitalsICH guidelinesIn VitroIn VivoKnowledge of the drug development processLaboratoryLaboratory ResearchLaboratory ManagementLaboratory SkillsLaboratory study designLaboratory TechniquesLC-MSLeadershipLife SciencesLiquid Chromatography-UV (LC-UV)Liquid chromatographyMedicineMetabolismMicrosoft ExcelMicrosoft OfficeMicrosoft PowerpointMicrosoft WordOutlookPharmaceutical DevelopmentPharmaceutical IndustryPharmaceuticalsPharmaceuticsPharmacistsPharmacokineticsPharmaceutical ResearchPharmaceutical SciencesPharmacyPowerPointPresentation SkillsProblem SolvingProject ManagementProtocolPublic SpeakingQA complianceQualificationQuality Assurance (QA)Quality AuditingQuality Control (QC)Quality ManagementR&DRegistration of the productRegulatory affairsRegulatory ComplianceRegulatory RequirementsRisk AssessmentScientific CommunicationsScientific WritingSocial SkillsSpectroscopySPSSStability testsStandard Operating Procedure (SOP)Statistical Data AnalysisStudy protocolsTeam BuildingTeam LeadershipTime ManagementTroubleshootingWriting Study Procedures and SOPs
LinkedIn Assessment :
Scientific WritingscienceMicroscopyLifesciencesBioinformaticsIn VitroSpectroscopyAnalytical ChemistryHPLCMass SpectrometryFDCgas chromatographyDLCCommunication SkillsUPLCAnalytical Method ValidationAnalytical Methods DevelopmentQuality ControlGMP

Skills and Expertise

Self Assessment :
Analytical skills Analyze data Assure medical quality Control data Create SOPs Develop protocols Guide students Interpret data Report data Search literature on clinical trials Use a confocal microscopy Write papers Write protocolsAssemble regulatory applicationsAssess product quality issuesAssign activitiesAttend seminars, courses and meetings within and outside the companyAttend seminarscollaborate in research projects at universitiesCollaborate with principal investigatorCollaborate with project teamCollect dataCommunicationCommunicate with sponsorCommunicate with investigatorConduct university research Conduct research at universitiesConduct studiesCoordinate projectsCreate SOPsCreate standard operating procedure (SOP)Creates a collaborative team environmentCoordinationcoordinating research projectsData miningData validationData verificationData entryDesign protocolsDesign protocolDesign studiesDesign studyDevelop ICH/GCP compliant processesDevelop protocolsDevelop strong internal relationships with stakeholdersDevelop study timelinesEstablish professional relationships with partnersEvaluate physico-chemical dataEvaluate protocolsEvaluate stability data Follow up training programsFollow-up of external auditsFollow-up of internal auditsFollow-up of quality assurance activitiesFollow-up of Quality Management System (QMS) processesGuide studentsInteract with pharmacistsInteract with regulatory stakeholdersInteract with statisticiansInterpret analytical resultsInterpret datalifescienceMaintain strong relationshipsManage global quality standardsManage laboratory proceduresManage multiple projectsManuscript preparationManuscript preparation and reviewManuscript reviewNetworkOral presentationPlan work to meet objectives and deadlinesPrepare external auditsPrepare final reportPrepare internal auditsPrepare manuscriptPrepare regulatory documentsPresent data at congressPublication of articlesQuality control processQuality testing of Investigational Medicinal Products (IMPs)R&DRead medical literatureRead medical literature to maintain current awareness and knowledgeRegulatory documentationResearch at universitiesRespond to audit findingsReview data interpretationReview protocolsReview quality control activitiesReview quality policiesReview study protocolsReview the interpretation of dataSolve problemsStatistical analysisUse laboratory techniquesValidate dataVerify dataUnderstand protocolsWork under specific instructionsWrite final reportsWrite papersWritten presentation

Education

  • Doctor in Pharmaceutical Sciences in Pharmaceutical Sciences from Ghent University in 2016
  • Master of Science in Drug Development in Pharmaceutical Sciences from Ghent University in 2012
  • Bachelor in Pharmaceutical Sciences in Pharmaceutical Sciences from Ghent University in 2010

Training and Certification

  • 9th World Mycotoxin Forum and XIVth IUPAC International Symposium on Mycotoxins, Winnipeg (Canada) in 2016 Training
  • 26th Pharmaceutical and Biomedical Analysis Symposium, Tbilisi (Georgia) in 2015 Training
  • Economic evaluations of medical interventions: specific training for researchers, Leuven (Belgium) in 2015 Training
  • 10th Drug Analysis and 25th Pharmaceutical and Biomedical Analysis Symposium, Liège (Belgium) in 2014 Training
  • 33rd European Peptide Symposium, Sofia (Bulgaria) in 2014 Training
  • Leadership Foundation Course, Ghent (Belgium) in 2013 Training
  • HPLC/UHPLC method development seminar, Brussels (Belgium) in 2012 Training
  • Mycoday, Liège (Belgium) in 2012 Training
  • Design of experiments (Umetrics Modde), Ghent (Belgium) in 2012 Certification
  • Multivariate data analysis (Umetrics Simca), Ghent (Belgium) in 2012 Certification

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Full Proficiency
French
Elementary Proficiency
German
Elementary Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Associate Scientist Biomedical Scientist Chemical Analyst Team Leader Team Assistant Senior Scientist scientific collaborator Scientific Advisor Scientific Associate Scientist Scientific Researcher Reviewer Clinical Data Reviewer Clinical Project Manager (CPM) Clinical Research Associate (CRA) Clinical Research Consultant Clinical Research Coordinator Clinical Research Manager Data Reviewer Data Manager Global Clinical Project Manager (GCPM, GTM) Global Data Manager Junior Consultant Junior Scientist Pharmacist QA Consultant QA Engineer QC/QA Manager Quality Assurance (QA) Manager QA Officer R&D Scientist Regulatory Affairs Officer Regulatory Affairs Consultant Regulatory Affairs Associate Project Manager Preclinical Scientist Preclinical Research Manager Preclinical Project Manager
  • Work From Home:
    No
  • Work Regime:
    Permanent position :    100% FTE
    BrightOwl employee :    100% FTE
  • International:
    Yes

Publications

    Expert has 13 publications (Will be avalible with full profile)

Area / Region

Waregem, Belgium

Others

Driving License
  • Yes

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