À propos de Olivier
Français
Bilingue ou natif
Anglais
Capacité professionnelle complète
Espagnol
Capacité professionnelle limitée
Italien
Capacité professionnelle limitée
Expériences
- Smart PhoenixOwneroctobre 2025 - Aujourd'hui (8 mois)Braine-l'Alleud, BelgiqueSociété de consultanceConsultance pour l'industrie pharmaceutique - spécialiséation en assurance qualité et digitalisationOffre de formation et coaching de professionnel pour entreprisesThématiques :- Utilisation de l'IA dans un cadre professionnel- Support à la digitilation et l'automatisation pour les services de département des ressources humaines- Support au repositionnement suite licenciementOffre de formation et coaching pour particuliers- Utilisation IA- personnes en recherche d'emploi
- POLYPEPTIDE,HEAD OF QUALITY ASSURANCEINDUSTRIE PHARMACEUTIQUEaoût 2023 - septembre 2025 (2 ans et 1 mois)BelgiumHeading QA Department in a Contract performing manufacturing and testing Overseeing a team of 50 professionals, including:• Quality Systems, Compliance & Audits team• Technical and qualification team• Quality Shopfloor team• Customer representative team• Continuous improvement teamMain responsibilities:• Ensure robust Quality Management Systems (QMS) are maintained and continuously improved• Define and implement Quality site remediation and improvement plan• Quality legal representative to Belgian Health Authorities (FAMHP)• Oversees inspection readiness and responses to audits from health authorities and commercial partners• Define and implement the overall QA strategy aligned with corporate objectives and site needs• Lead internal and external audits, drive deviation and CAPA management and risk mitigation strategies• Oversee validation activities: equipment, processes, cleaning, and computerized systems• Act as key decision-maker on complex deviation investigations, change controls and product release• Liaise with regulatory authorities and commercial partners on quality-related matters• Participate in cross-functional leadership teams to align quality with operations and supply chain• Quality management of product lifecycle including process transfer from / to other sites• Review and approve commercial product quality annual report (PQR)• Budget management of the QA department
- GSK VACCINES,QC MANAGER - SME DATA INTEGRITYINDUSTRIE PHARMACEUTIQUEmai 2022 - août 2023 (1 an et 3 mois)BelgiumData Integrity (DI) subject matter expert for Quality Control (QC) and Incoming Material (IM) departments – Coverage spans a 1,200 personnel DI representative at the Belgium level memberMain responsibilities:• Supporting DI risk assessments for deviations, CAPA and change control• Owner of risks related to DI topics• Oversight during audits and regulatory inspections• Deploy DI policies and procedures and lead training programs related to data integrity standards• Define and implement the Data Integrity Roadmap for QC & IM departments• Ensure alignment with global regulatory expectations and corporate objectives• Lead DI gap assessments and remediation plans for electronic systems and lab instruments• Establish performance metrics for DI monitoring and reporting• Participate in data & digital initiatives
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Formations
- Biotech EngineerENSTBB2007Biotech Engineer
- BACHELOR OF SCIENCESLE CHESNOY2004BACHELOR OF SCIENCES
Compétences
Catégories
- Autre