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Summary

Open for professional challenges and to enlarge my professional expertise. current main responsibilities: ● Dossier compilation, submission and follow up in EU for . * biocides . * veterinary medicines . * detergents . * poison center notifications . Support for rest of EMEA region ● writing of . * stability reports . * environmental risk assessments . * human risk assessments . * clinical export reports ● compilation of safety datasheets in compliance with REACH and CLP ● REACH responsible for EU production sites

Experiences

Current Experience

  • Regulatory Affairs Associate
    Since March 2013

Past Experience

  • Product Regulatory Advisor
    August 2009 --- March 2013

  • PhD student
    August 2004 --- July 2009

  • .
    January 1901 --- January 1901

Knowledge

LinkedIn Assessment :
Regulatory affairsChemistryBiocidesProduct StewardshipEHSREAChPolymersR&DChemical EngineeringPolymer ChemistryTPUVeterinary MedicineCLPGHSLevenswetenschappenBiotechnologie

Skills and Expertise

Self Assessment :
REAch

Education

  • Master of Biotechnology in from University of Ghent in 2003

Training and Certification

  • Bachelor of Biology Certification
  • Basic Course in Laboratory Animal Science (cat. C) Certification
  • Doctor in Sciences: Biochemistry Certification
  • Master of Biotechnology Certification
  • Methods in Molecular Biotechnology (MaNaMa) Certification

Area / Region

Hertsberge, Oostkamp, Belgium

Others

Driving License
  • No