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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 StewardshipEHSREAChPolymersChemical 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 in 0000 Certification
  • Basic Course in Laboratory Animal Science (cat. C) in 0000 Certification
  • Doctor in Sciences: Biochemistry in 0000 Certification
  • Master of Biotechnology in 0000 Certification
  • Methods in Molecular Biotechnology (MaNaMa) in 0000 Certification

Area / Region

Hertsberge, Oostkamp, Belgium

Others

Driving License
  • No

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