SANOFI

Informations sur l'entreprise

Nom de l'entreprise : SANOFI
Ville : Val-de-Reuil 27101

Détails du contrat

Type de contrat : cdi
Type de métier : CMC Development
Date de publication: 18/02/2023
Offre

A propos du recruteur

La vocation de Sanofi est d?accompagner celles et ceux confrontés à des difficultés de santé. Entreprise biopharmaceutique mondiale spécialisée dans la santé humaine, nous prévenons les maladies avec nos vaccins et proposons des traitements innovants. Nous accompagnons tant ceux qui sont atteints de maladies rares, que les millions de personnes souffrant d?une maladie chronique. Sanofi et ses plus de 100 000 collaborateurs dans 100 pays transforment l?innovation scientifique en solutions de santé partout dans le monde. Sanofi, Empowering Life, donner toute sa force à la vie. Chez Sanofi, la diversité et l?inclusion sont au c?ur de notre fonctionnement et sont intégrées à nos Valeurs fondamentales. Nous sommes conscients que pour exploiter véritablement la richesse que la diversité nous apporte, nous devons faire preuve d?inclusion et créer un environnement de travail où ces différences peuvent s?épanouir et être développées pour améliorer le quotidien de nos collègues, patients et clients. Nous respectons et valorisons la diversité de nos collaborateurs, leurs parcours et leurs expériences dans un objectif d?égalité des chances pour tous.

Description du poste

Sanofi Pasteur est l’un des leaders de l’industrie du vaccin depuis plus de 100ans et un partenaire mondialement reconnu pour la prévention des maladies infectieuses. Nous croyons à un monde dans lequel personne ne souffre ou ne meurt d’une maladie évitable par la vaccination. ​ Le site de Val-de-Reuil est le site de référence pour la production du vaccin contre la grippe (130 millions de doses produites chaque année) et la fièvre jaune, qui sont ensuite distribués à travers le monde. Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l'anglais étant la langue de travail. ABOUT THE JOB Our Team Our team is part of “Science & Techno Excellence”, which is an entity of Manufacturing Technology. The mission of the Global Manufacturing Technology is to manage and ensure the industrialization of Vaccines to support Sanofi Vaccines ambition. The Scientific and Techno Standards & Best practices team is in this ambition, and is dedicated as a global function to drive the standardization of bioprocesses in the fields of vaccines and to promote its deployment within projects and on industrial sites. Thus, our mission is to develop Sanofi Vaccines’ best practices and standards, particularly in bioprocesses, in order to maintain its progress in innovation, simplification and intensification while maintaining industrial excellence. Job title: Scientific & Techno Standards Project ManagerGrade: 2.1Location: Val de ReuilRemote: Full time job with possible remote Work 2 days/week; Low frequency of Business travelsJob type: CDI de chantier Full time Main responsibilities Under the direction of the Global Scientific & Techno Standard Leader, the Scientific & Techno Standards Project Manager is a transversal function aiming to deploy the roadmap of the Sc&T Standards & best practices, while being the methodology referent for expert teams, coordinating actions & teams to build the Standards, and ensuring the preparation of the evaluation body allowing the endorsement and the diffusion of these standards. The design & implementation of the Scientific & Techno standards built in partnership with the multiple actors (among Research & Development and Industrial Affairs) will maximize from short to long term the industrial landing of new vaccines or current vaccine redesigned processes in new facilities. At Sanofi group level, He/She will contribute to promote, communicate and support the implementation of standards and Best practices as a tool for innovation and performance improvement. The mission described is carried out in a GMP environment, in compliance with health, safety and environmental rules and in compliance with the site's quality procedures. As Scientific & Techno Standards Project Manager Ensure the coordination and the design of new Scientific and Technos standards according to the defined roadmap, etc.Organization and preparation of working sessions and management of the progress of working groups on standardsPreparation of technical topics and presentations with expertsUpdate of the Manufacturability toolMonitoring of the implementation of the Roadmap Standards & Best practicesPrioritization of Scientific & Techno Standards subjects to ensure the achievement of Key Performance IndicatorsPreparation with the team members of the monthly highlights Coordinate scientific working groups (Experts teams) during the evaluation of New Vaccines projects in order to determine their level of Industrial "manufacturability" and standardization according to the defined roadmapConducting Manufacturability/Developability exercises with the global standard leaderWriting corresponding reports Coordinate key bodies and meetings and ensure they are held within the defined deadlinesManaging the bodies/meetingsExpert committees such as the SEC Standards Evaluation CommitteeWorking groups on standards (Kick-off meeting, working group meetings, etc.) Writing of the Reports and implementation/managing of the actions defined into the minutes in collaboration with the experts/co-referents and the Standards manager Guarantee the document management of the Scientific and Technical Standards and the communication on the StandardsImplementation definition, and implementation of standards validated on Quality Corporate DocumentationManaging updatesWebinars design or other way of communication, according to the defined roadmap, in collaboration with the Standards & Best practices team Ensure reporting, within the scope of her/his activities, to direct management, in order to receive feedback, and guarantee effective cross-functional operation with the other functions involved in Standards & Best Practices and site functions ABOUT YOU Experience More than 3 years’ experience in Bio pharmaceutical companyTransversal management experience Soft skills Ability to succeed in a team-oriented environment under very dynamic conditionsAbility to deliver projects with complex requirements and a strong customer focusAbility to influence and communicate with a diverse group of stakeholders and from multiple worldwide sitesTeam spirit/Cooperate Transversally/Strive for Results Technical skills Wide scientific, technical & industrial backgroundTransversal Management (Project management, portfolio management)Network Leadership, CommunicationInnovation spirit, Knowledge transmission Education Engineer or PhD in biosciences (biotechnology, bioprocessing or analytical sciences) or Project Management Languages French & English (spoken and written)English: at minimum B2 level required - C1 ideal

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