{"id":884,"date":"2026-09-11T09:32:21","date_gmt":"2026-09-11T07:32:21","guid":{"rendered":"https:\/\/madeconseil.com\/?post_type=offres&p=884"},"modified":"2026-09-11T09:33:48","modified_gmt":"2026-09-11T07:33:48","slug":"charge-dassurance-qualite-systeme-gestion-documentaire-h-f","status":"publish","type":"offres","link":"https:\/\/madeconseil.com\/en\/offres\/charge-dassurance-qualite-systeme-gestion-documentaire-h-f\/","title":{"rendered":"Charg\u00e9 d’Assurance Qualit\u00e9 Syst\u00e8me – Gestion Documentaire H\/F"},"content":{"rendered":"

\nCharg\u00e9 d'Assurance Qualit\u00e9 Syst\u00e8me - Gestion Documentaire H\/F\n<\/h1>

\nBuild a career that matters.\n<\/h2>

At made., we have built a model that allows consultants to commit to demanding projects without sacrificing either their work-life balance or their professional trajectory.
We see engineering consulting as a true profession, practiced at the heart of our clients\u2019 projects.
We support healthcare industrial players in their most critical quality projects, within demanding regulated environments: pharmaceutical, biotech, medical devices.
Above all, we have chosen to break down silos and unlock career paths by putting people back at the center of consulting.
Here, you work on projects that matter, within a socially committed framework, with a trajectory designed for the long term.<\/p>

\nYour role\n<\/h2>

\nNous recherchons un(e) Charg\u00e9(e) d'Assurance Qualit\u00e9 Syst\u00e8me pour rejoindre nos \u00e9quipes et intervenir au sein d'un environnement pharmaceutique sur des enjeux de gestion documentaire, archivage et audits.
Vous \u00e9voluez dans un contexte de transformation des outils documentaires, avec notamment un projet de migration de WebDoc vers Veeva.

En tant que consultant made., vous contribuez au bon fonctionnement et \u00e0 l'am\u00e9lioration du syst\u00e8me de management de la qualit\u00e9, avec une forte orientation gestion documentaire.

Vous veillez \u00e0 la ma\u00eetrise, \u00e0 la conformit\u00e9 et \u00e0 la tra\u00e7abilit\u00e9 de la documentation qualit\u00e9 et accompagnez les diff\u00e9rents m\u00e9tiers dans l'application des processus associ\u00e9s.

Vous participez \u00e9galement aux activit\u00e9s d'audit et contribuez \u00e0 la pr\u00e9paration de la transition vers un nouvel environnement documentaire.

\n<\/p>

\nYour day-to-day
\n<\/h2>

\nVous serez notamment amen\u00e9(e) \u00e0 :

assurer la gestion et le suivi de la documentation du syst\u00e8me qualit\u00e9
contribuer \u00e0 la cr\u00e9ation, la r\u00e9vision, l'approbation et la diffusion des documents qualit\u00e9
veiller \u00e0 la conformit\u00e9, \u00e0 la tra\u00e7abilit\u00e9 et au respect du cycle de vie documentaire
assurer le suivi des activit\u00e9s d'archivage et garantir la bonne conservation de la documentation
accompagner les diff\u00e9rents m\u00e9tiers dans l'utilisation et l'application du syst\u00e8me documentaire
contribuer \u00e0 la pr\u00e9paration, \u00e0 la r\u00e9alisation et au suivi des audits qualit\u00e9
participer au suivi des actions issues des audits
contribuer \u00e0 l'am\u00e9lioration continue des processus documentaires et du syst\u00e8me qualit\u00e9
participer \u00e0 la pr\u00e9paration et \u00e0 l'accompagnement de la migration de WebDoc vers Veeva
contribuer \u00e0 la fiabilisation et \u00e0 la reprise de la documentation dans le cadre de cette transition
identifier les \u00e9carts ou points de vigilance et coordonner les actions n\u00e9cessaires avec les diff\u00e9rents interlocuteurs
assurer le suivi et le reporting des activit\u00e9s de votre p\u00e9rim\u00e8tre\n<\/p>

\nYour profile\n<\/h2>

\nIssu(e) d'une formation Bac +5 scientifique, pharmaceutique, qualit\u00e9 ou \u00e9quivalent, vous disposez d'une exp\u00e9rience en Assurance Qualit\u00e9 Syst\u00e8me dans l'industrie pharmaceutique.

Vous ma\u00eetrisez les fondamentaux de la gestion documentaire en environnement BPF\/GMP et comprenez les exigences associ\u00e9es \u00e0 la ma\u00eetrise du cycle de vie des documents qualit\u00e9.

Vous disposez de connaissances ou d'une exp\u00e9rience sur plusieurs des sujets suivants :

Assurance Qualit\u00e9 Syst\u00e8me
gestion documentaire
archivage qualit\u00e9
audits internes et\/ou externes
syst\u00e8mes de management de la qualit\u00e9
BPF \/ GMP
outils de gestion \u00e9lectronique documentaire
migration ou \u00e9volution d'un syst\u00e8me documentaire

Une exp\u00e9rience sur Veeva constitue un v\u00e9ritable atout. Une connaissance de WebDoc sera \u00e9galement appr\u00e9ci\u00e9e dans le contexte du projet de migration.

Au-del\u00e0 de la ma\u00eetrise des outils, nous recherchons surtout une personne rigoureuse, structur\u00e9e et capable de comprendre rapidement un environnement qualit\u00e9 et ses processus.

Vous \u00eates \u00e0 l'aise avec la gestion documentaire, savez travailler avec de nombreux interlocuteurs et faites preuve d'autonomie et de pragmatisme pour rechercher l'information et faire avancer vos sujets.\n<\/p>

\nWhy join made.?\n<\/h2>

Joining made. means:

\u2022 practicing consulting as a true profession,
\u2022 working on structuring projects, not opportunistic assignments,
\u2022 growing through the diversity and complexity of client projects,
\u2022 being supported in your development through a simple, direct relationship,
\u2022 building a coherent and evolving professional trajectory.

Want to learn more?

We take the time to talk.
Send us your application in complete confidentiality.<\/p>\nAPPLY\n<\/a><\/div>","protected":false},"template":"","class_list":["post-884","offres","type-offres","status-publish","hentry"],"acf":[],"yoast_head":"\nCharg\u00e9 d'Assurance Qualit\u00e9 Syst\u00e8me - Gestion Documentaire H\/F - Made Conseil<\/title>\n<meta name=\"description\" content=\"Offre d\u2019emploi Ing\u00e9nieur\u00b7e Qualit\u00e9 \u2013 Industrie pharmaceutique (H\/F). 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