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i am currently working as a Regulatory Affairs officer and i am on the lookout for a new Career direction.

i am particularly interested by the regulatory framework of medicines and Health products, that’s why participating in the Clinical Development and Market access of innovative products motivates me.

i am eager to develop my skills in Regulatory Affairs and ready for a new challenge.


Current Experience

  • Regulatory Affairs Officer

    Since January 2015
    • writing Marketing authorisation dossier for homeopathic medicinal products • Compliance with national and european regulatory frameworks • reviewing scientific and legal documentations • compiling modules 3 and 4 of the ctd • participation in Strategy meetings • Writing marketing authorisation dossier for homeopathic medicinal products • Compliance with national and european regulatory frameworks • Reviewing scientific and legal documentations • Compiling modules 3 and 4 of the CTD • Participation in strategy meetings

Past Experience

  • Research Scientist

    February 2012 --- July 2014
    Clinical research: participation to the raidgbs project funded by the walloon region : development and Validation of a new test for the rapid and easy identification of group b streptococcus in pregnant women • Quality Assurance : Validation files and SOP writing for Analysis that will be accredited by belac under the standard ISO 15189 in the Laboratory of infectious serology • involvement to the activities and development of the national reference centers for streptococcus agalactiae and mycoses • evaluation and Validation of new tests in Bacteriology and molecular biologySupervisor of Microbiology practicals

  • Research Scientist

    October 2009 --- January 2012
    • development of a Preclinical model of cystic fibrosis and Characterization of In Vivo efficiency of a new antibiotic Treatment • development of new therapeutic strategies against bronchial carcinoma


Self Assessment :
Analytical thinkingAttention to detailCollaborationSociabilityFlexibility


LinkedIn Assessment :
Regulatory affairsQA/QCClinical researchReport WritingProtocol WritingMicrobiologymolecular biologyAnalytical Method ValidationAnimal handlingBiologie molBiotechnologie


  • in Regulatory Affairs Manager from GIGA Biotechnology Training Center in 2014
  • Master's degree in Biomedical sciences from University of Liege in 2009


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Locations I am interested in:
    Walloon Region, Belgium
  • Work From Home:
  • International:

Area / Region

Liège, Belgium


Driving License
  • Yes

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