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9 years experienced, with specific skills in Qualification (equipment and utilities), project management (PRINCE 2 Certified), product transfer, operational quality assurance and EHS subjects for the pharmaceutical and cosmetic industries. Competences on: - Commissioning and Qualification - Project Management (Prince 2 certified) - Team management - Training Specialties: - Qualification and Validation project management - Product transfer - Quality Assurance - Engineering - Process optimization (Lean Manufacturing methodologies) - EHS (internal audit and ISO14001)


Current Experience

  • Validation Engineer via Nalys
    Since May 2016

  • Specialist Consultant - PRISM member
    Since October 2015
    PRISM (PRoject Innovation Services Management) is a Nalys internal department dedicated to innovation As a PRISM member, I am involved in the training support (as internal trainer and coach) and in developing the internal professional library. • Trainer o Planning and lead of training sessions (including Good Distribution Practices, Introduction to Prince 2…) and certification associated o Development of training supports and templates o Technical review of training supports • Training process o Improvement of training process o Managing training partnership with European training organization • Case study support o Creation of practical case study o Coaching during case study period • Professional Library o Creation of an electronic database providing GxP Guidance and Regulatory documents o Managing the internal professional library in selecting professional books and in developing referencing method

Past Experience

  • Decommissioning coordinator consultant (Nalys)
    October 2015 --- November 2015
    Decommissioning coordination for a complete plant after closure.

  • Qualification engineer
    December 2011 --- September 2015
    - Qualification Coordination (equipment, utilities, HVAC with Building Management System, building) - Project leading - Supplier coordination - Calibration coordination - SOPs update and creation - EHS support for local safety manager (CPPT secretary, EHS internal audit, ISO14001 pre-certification, ATEX certification ...) - Emergency coordinator - EPI (First Intervention in case of emergency)

  • Process Validation - Industrialization at GSK Biological
    November 2010 --- December 2011
    - Update of Categorization of Process Parameters documents - Review of validation document - Review of Vaccine transfer document to CMO - Review of transversal documents

  • Consultant
    June 2008 --- December 2011

  • Qualification Engineer at Besins Healthcare
    June 2010 --- November 2010
    o Create decommissioning, FAT and qualification protocol and report template according to the new qualification procedure o For a complete filling line : 1. Writing Qualification Plan 2. Writing decommissioning protocol 3. Writing FAT protocols and reports 4. Realization of FAT tests 5. Writing qualification protocols and reports 6. Realization of qualification tests o Writing part of building qualification protocols and reports (5 areas)

  • Team leader support at Catalent New Product Introduction/Process Validation
    March 2010 --- June 2010
    o Redaction of product plan validation, process validation, BOM, batch records, reports (manufacturing and packaging) o Redaction of regulatory documents and procedure o Sharing documents with internal experts and clients o Implementing comments o Tracking document during final validation.

  • Quality assurance engineer at Baxter R&D Belgium
    April 2009 --- March 2010
    o Participation to creation and updating of action plan defining the planning of procedures and forms creation. o Creation and updating of different indicators to follow the mission advancement. o Follow-up of documents approval. o Redaction of procedures and associated forms for the entire department (General, Mixing, Filling, calibration, …). o Adaptation of existing procedures and forms to integrate the new department. o Training of involved people to procedures and forms used (from managers to operators). o Participation to concrete decision making for the Pilot plant implementation (flux, security equipments, ...)

  • Periodic qualification evaluation coordinator at Baxter Lessines
    June 2008 --- April 2009
    o Participation to periodic evaluation template improvement o Evaluation of existing qualification and validation documentation o Check of installation o Evaluation to conformity with current regulation o Critical assessment o Creation of action plan template o Redaction of action plan (determining action) o Redaction of a Validation Master Plan for the Medical Devices service (Extrusion, Plastic Bag production, Molding) o Research and reading of all the documentation (procedures, qualification and validation reports) about equipments and processes used in the Medical Devices service) o Redaction of Qualification and Validation protocol and report

  • Production Engineer
    March 2007 --- December 2007
    o Spatial and ergonomic modifications o Circulation flux reorganisation under Microsoft Visio o Day by day schedule under Microsoft Project o Relationship with suppliers (Need in test materials, in equipments, in information) o Creation of FAT/SAT template protocols o Equipment validation under the L’Oréal and APAVE standards (FAT, SAT) o Supervision of the packaging line installation by suppliers (from product filling to palletizing robot) o Establishment of continuous improvement and training of the technical staff o Review and redaction of good practice presentation o Improvement and installation of “Zero default” system o Setting of L’Oréal production gauging software program and official presentation


Self Assessment :
AdaptabilityAttention to detailCharmCommunicativeCoordinationCuriosityEfficiencyOptimismProactivityReaction to stressSociability


LinkedIn Assessment :
EPISOPFDAProject ManagementGXPConsultingmanagementValidationQuality AssuranceProcess ValidationCoachingV&VProduct TransferSOPChange ControlEHSATEXEquipment QualificationQualification TestingTeam ManagementPRINCE 2 certifiedBA4 certificationPharmaceutical IndustryGMPTesting

Skills and Expertise

Self Assessment :
Create SOPs Develop protocols Guide students Interpret data Report data Write protocolsAdvise on strategyArchive documentationCoachCollaborate with project teamcontrol different protocol versions and other essential documentsCoordinate projectsCoordinationCreate SOPsDevelop protocolsDevelop training materialsIdentify risksImplement Key Performance Indicators (KPI's)lifescienceManage contractors Oral presentationPeople managementProtocol managementProvide trainingReview protocolsSelect contractors Train off site staffUnderstand protocolsWrite documentsWrite final reports


  • Engineer in Food Industry from Polytech'Montpellier in 2007
  • ERASMUS in Management, Marketing and Communication from Wageningen University in 2007

Training and Certification

  • BA4 Certification
  • Maxer Method (Failure and Breakdown diagnostics method) Certification
  • Prince 2 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Elementary Proficiency

Work Preferences

  • Locations I am interested in:
  • Work From Home:
  • Work Regime:
    Permanent position :    100% FTE
  • International:

Area / Region

Brussels, Belgium


Driving License
  • Yes