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Experiences

Current Experience

  • Associate Scientist
    Since January 2011
    Parenterals and Liquids group: department of Pharmaceutical Development and Manufacturing Sciences -Drug Product Development (PDMS-DPD). Responsible for end-to-end drug product development for large and small molecules including: - Formulation development activities for oral and parenteral administration for early, mid and late stage molecules - Process development activities for oral and parenteral formulations - Formulation and process transfer activities to pilot and manufacturing plants - Life cycle management and support of operations at pilot and manufacturing plants. - Development of liquid formulation technologies to enhance patient compliance such as pediatric formulations and injectable sustained delivery systems

Past Experience

  • Associate Scientist
    November 2014 --- July 2015
    Phamaceutical and Material Sciences - Particle and Powder Characterization: department of Pharmaceutical Development and Manufacturing Sciences -Drug Product Development Characterization activities related to particle properties (such as size, morphology, surface area, brittleness etc.) and powder behavior (such as powder flow, wettability, etc.) in support of crystallization development & milling activities, drug product development, troubleshooting activities and LCM.

  • Research Assistant
    January 2011 --- October 2014
    Parenterals and Liquids group: department of Pharmaceutical Development and Manufacturing Sciences -Drug Product Development (PDMS-DPD).

Personality

Self Assessment :
DiligenceAttention to detailInterest in knowledgeProblem solvingStrategic thinkingEfficiencyCuriosity

Knowledge

Self Assessment :
Validation
LinkedIn Assessment :
Formulation developmentPharmaceutical process developmentKnowledge ManagementPharmaceutical ManufacturingGMPDrug ProductPharmaceutical IndustryGood Laboratory Practice (GLP)Particle CharacterizationProject ManagementNanotechnologyDrug DevelopmentFormulationProcess improvement

Education

  • Clinical Research in Biomedical Sciences, General from Katholieke Universiteit Leuven in 2012
  • Bachelor in Biomedical Laboratory Technology in Pharmaceutical and Biological Siences from Katholieke Hogeschool Leuven in 2011

Training and Certification

  • Drug development process: From discovery to commercialization (CFPIE) in 2014 Training
  • Parenteral Products (European Continuing Education College) in 2014 Training
  • BePCIS: Particle Characterization in 2013 Training
  • Method Development on Malvern Mastersizer 3000 in 2014 Certification
  • Stat-Ease: Designed experiments for Pharma in 2014 Certification

Languages

BrightOwl Assessment:
Self Assessment:
English
Full Proficiency
Dutch
Native

Area / Region

Geel, België

Others

Driving License
  • Yes