About Danfeh
French
Native or bilingual
English
Fluent
Experience
- SanofiIndependent Consultant AMOA Doc ControllerPHARMACEUTICALS INDUSTRYJanuary 2024 - Today (2 years and 5 months)Neuville-sur-Saône, FranceSanofi 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 - EFORConsultant Lead Doc ControllerPHARMACEUTICALS INDUSTRYJanuary 2023 - January 2024 (1 year)Lyon, FranceConsultant 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..
- CGIConsultant IS Functional AdministratorPHARMACEUTICALS INDUSTRYFebruary 2022 - December 2022 (10 months)Lyon, FranceConsultant as IS functional administrator for the Servier groupManagement 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.
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Education
- Master of Scientific and Technical InformationENSSIB - Lyon 12017
Certifications
- Pharma Computer System Validation (CSV & Quality)Udemy2025
- Good Manufacturing Practices (GMP – EU GMP)E-Learning2024