About Mamadou
Senior Consultant specialising in Quality Applications and Digital Transformation in GxP-regulated environments, with more than 10 years of experience in the pharmaceutical and life sciences industries.
Extensive experience acting as Business System Owner and Subject Matter Expert for Quality applications, including Veeva Vault QMS and QualityDocs, supporting global organisations in system deployment, lifecycle management, validation readiness, and process optimisation.
Proven ability to translate business requirements into scalable digital solutions, coordinate system changes and releases, and drive continuous improvement of regulated Quality platforms
French
Native or bilingual
English
Fluent
Can work on-site
Orléans (up to 50km)
Experience
- SanofiSenior Consultant – Business System OwnerPHARMACEUTICALS INDUSTRYJanuary 2021 - October 2025 (4 years and 9 months)Lyon, FranceProject: Global deployment and optimisation of to replacePhenix : legacy Quality systems. Key responsibilities:• • Acted as Business System Owner for Quality applications, ensuring alignment between IT, Quality teams and external vendors.• • Managed application lifecycle activities, including configuration workshops, change requests, and system improvements.• • Collected and analysed business requirements from Quality stakeholders, translating them into functional specifications and system configurations.• • Coordinated system validation activities within an Agile environment (JIRA), ensuring compliance with GxP requirements.• • Led testing phases including FUT, SIT and UAT, ensuring validation readiness and regulatory compliance.• • Delivered training sessions and supported global adoption for more than 250 users.
- Parfums Christian DiorDocument Management & QMS Deployment LeadFASHION AND COSMETICSJanuary 2018 - January 2020 (2 years)Orléans, FranceProject: Implementation of Veeva Vault QMS to replace Open Text : legacy document management systems and Doc manager
- Air Liquide Medical SystemsQuality TechnicianMEDICALJanuary 2017 - January 2018 (1 year)Antony, France• • Supervised Device History Record (DHR) release activities.• • Analysed non-conformities and quality control data.• • Led problem-solving activities (A3, 5 Why, Ishikawa, 8D).• • Contributed to continuous improvement initiatives to strengthen regulatory compliance.
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Education
- Specialized Master's in Quality ManagementArts et Métiers ParisTech2021Specialized Master's in Quality Management
- TOSA CertificationIFIS PharmaTOSA Certification