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Current Experience

  • Consultante
    Since March 2016

  • Project engineer - Validation & Qualification
    Since March 2016

    I take part of a revamping project of bioreactors, for the qualification and validation. The project is composed of about 20 engineers. I’m part of the SIP team which is responsible for the qualification and validation of all SIP cycles on bioreactors and its associate loops. More specifically, my job is : - Analyze of execution runs and documentation of these runs - Ruling about conformity of execution runs - Management of deviations and CAPA related to protocols - Review and completion of protocols after their execution

Past Experience

  • Finishing Coordinator
    August 2013 --- March 2016

    I coordinate all operations gravitating around the filling line under an isolator, in collaboration with the maintenance, calibration, automation, engineering, validation, supply chain, environment monitoring and quality departments. The team is composed of 2 coordinators, 1 supervisor and 3 foremen with their respective team, one for each shift. We are responsible of the respect of the committed filling capacity on our production line (including implications on vial’s washing machine, sterilization tunnel, filling, stoppering, capping, crimping and printing station, palletizing unit and cleaning out of place). More specifically, my job is - Management of the production planning, including preventive maintenance, calibrations and engineering tests - Creation and management of procedures, in collaboration with validation, maintenance, calibration, automation, engineering, validation, environment monitoring and quality departments - Management of continuous improvement projects in aseptic production areas using DMAIC methodology such as SMED, DDFP, Standard Work and visual aids - Investigation during unusual events via the CAPA management system and associated actions - Coordination of IT changes for the Electronic Batch Management - Active participation in Change Control via the emission, management and coordination of changes - Read and understand different guidelines (FDA, GMP) in collaboration with quality - Training of people to ensure respect of Good Manufacturing Practices and procedures


Self Assessment :
AdaptabilityCollaborationAttention to detailCommunicativeCoordinationEfficiencyFlexibilityIndependenceOrganizationProblem solvingResult Oriented


LinkedIn Assessment :
MaCoordination de projetOutils LeanSecteur pharmaceutiqueLean ManufacturingMatlabIngValidationCAPAChange Management

Skills and Expertise

Self Assessment :
Analytical skills Create SOPs Interpret data Report dataAseptic processingAseptic techniquesAssess quality process issuesAssess product quality issuesCollaborate with project teamCollaborate with principal investigatorCoordinate projectsDesign efficiency studyDesign IT solutionsEnsure data consistencyImplement Key Performance Indicators (KPI's)Interpret dataManage aseptic riskManufacture of GMP batchesMonitor Key Performance Indicators (KPI's)Prepare external auditsproject managementProvide trainingReview protocolsSolve problems


  • Ingénieur Civil in Biomédical from Université catholique de Louvain in 2013

Training and Certification

  • Lean Green Belt Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Biomedical Scientist Business Consultant Business Development Manager Data Manager Data Reviewer Development Manager Engineer Equipment Engineer Field Clinical Engineer Field Service Engineer GMP Coordinator Junior Consultant Junior Scientist Lead Consultant Management Consultant Process Engineer Principal Scientist Product Specialist Production Manager Product Manager Production Supervisor Project Manager Project Leader Project Engineer QA Engineer QA Consultant Project Assistant QA Lead QA Officer QC/QA Manager Quality Assurance (QA) Manager Quality Engineer Quality manager R&D engineer Regulatory Affairs Consultant Scientific consultant scientific collaborator Scientist Supply chain planner Team Leader
  • Locations I am interested in:
  • Work From Home:
    Yes, 0 to 4 days per week
  • International:

Area / Region



Driving License
  • Yes