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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 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

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

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