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Danfeh BouhDB

Danfeh Bouh

Document Management Expert Consultant

€700/day
Lyon, FR
3-7 years

Average response time: 1 hour

Freelancer profile translated to English.
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About Danfeh

Experienced IS functional administrator with proven expertise in managing technical and administrative documentation on complex projects, particularly in the automotive, R&D, and pharmaceutical industries. I possess a strong command of information and document management systems, as well as experience in database administration, ensuring optimal information management throughout the project lifecycle.
  • French

    Native or bilingual

  • English

    Fluent

Can work on-site
Lyon (up to 50km)

Experience

  • Sanofi
    Independent Consultant AMOA Doc Controller
    PHARMACEUTICALS INDUSTRY
    January 2024 - Today (2 years and 5 months)
    Neuville-sur-Saône, France
    Sanofi launched an innovative project named 'EVF' (Evolutif Vaccine Facility), renamed 'Modulus' after its official inauguration by institutional representatives. This ambitious project aims to build a revolutionary vaccine production site in Neuville-sur-Saône, with a second site in Singapore, designed with the same configurations. This initiative marks a significant step in optimizing and modernizing vaccine production globally.

    Responsible for deliverables management for engineering systems (C&Q).
    • Analysis and data management of various tools.
    • Monitoring of review/approval deadlines and management of supplier DEDs.
    • Creation of Power BI dashboards for KPIs and documentation processes.
    • Collaboration with PMOs and engineers for optimal workflow management.
    • Expertise in document management to ensure the integrity, traceability, and compliance of technical documents throughout the project lifecycle.
    • Monitoring of equipment qualifications (Gxp, Non Gxp, HSE etc.) up to installation (OQ, IQ, PQ).
    • Management of change controls with quality assurance, maintenance, production, automation, etc..
    Tools: SharePoint, Veeva Vault, GEDMS, Kneat, Power BI, One Lims, Gaje Insights
    GxP Microsoft SharePoint Veeva Vault GEDMS Commissioning & Qualification
  • EFOR
    Consultant Lead Doc Controller
    PHARMACEUTICALS INDUSTRY
    January 2023 - January 2024 (1 year)
    Lyon, France
    Consultant as commissioning and qualification document controller at Sanofi, EVF project.

    Responsible for deliverables management for engineering systems (C&Q).
    • Analysis and data management of various tools.
    • Monitoring of review/approval deadlines and management of supplier DEDs.
    • Creation of Power BI dashboards for KPIs and documentation processes.
    • Collaboration with PMOs and engineers for optimal workflow management.
    • Expertise in document management to ensure the integrity, traceability, and compliance of technical documents throughout the project lifecycle.
    • Monitoring of equipment qualifications (Gxp, Non Gxp, HSE etc.) up to installation (OQ, IQ, PQ).
    • Management of change controls with quality assurance, maintenance, production, automation, etc..
    VSI V-Cycle BPF LIMS Veeva Vault
  • CGI
    Consultant IS Functional Administrator
    PHARMACEUTICALS INDUSTRY
    February 2022 - December 2022 (10 months)
    Lyon, France
    Consultant as IS functional administrator for the Servier group

    Management of documentary systems for regulatory affairs and pharmacovigilance.
    • Management of user and administration documentation (guides, memocards, training materials, etc.)
    • Database administration and quality control of user access.
    • Analysis of client data for reporting and decision-making.
    • Management of IS evolutions and user support.
    • Administration of chemical, documentary, and regulatory databases.
    • Quality control of files before submission to the State in regulatory databases.
    Regulatory Affairs Functional Administration Data Analysis eTMF User Support

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Education

  • Master of Scientific and Technical Information
    ENSSIB - Lyon 1
    2017

Certifications

  • Pharma Computer System Validation (CSV & Quality)
    Udemy
    2025
    V-Cycle Data Integrity & ALCOA+ (Documentation & Records)
  • Good Manufacturing Practices (GMP – EU GMP)
    E-Learning
    2024
    SOP BPF GMP GxP

Skill set

Categories