Preclinical Quality Assurance Technician 1

il y a 3 jours

Paris, Île-de-France Veranex, Inc. Temps plein

Veranex est le seul fournisseur de services technologiques véritablement complet et mondial dédié à l'industrie des technologies médicales. Veranex offre des conseils d'experts de la conception à la commercialisation, y compris la conception et l'ingénierie des produits, le développement préclinique et clinique, la gestion des données, l'accès au marché, les affaires réglementaires et l'assurance qualité. Veranex permet d'accélérer la mise sur le marché, de contrôler les coûts de développement, d'atténuer les risques de développement et d'accélérer l'évaluation de la viabilité du marché. À chaque étape, les clients de Veranex réalisent des gains de temps et d'argent, tandis que nos solutions complètes unifient l'ensemble du processus de développement. Veranex s'associe aux entreprises les plus influentes du monde dans le domaine des sciences de la vie et des dispositifs médicaux pour rechercher, concevoir, développer et commercialiser de nouvelles technologies et de nouveaux traitements dans le domaine de la santé, afin de faire progresser les soins aux patients. Your MissionsUnder the supervision of the Quality Service Manager, you will be responsible for the following tasks:Ensure HSE monitoring, as well as update the Single Occupational Risk Assessment Document (DUERP) for our two sites, and play an active role in occupational risk prevention among staff.Plan and carry out audits of the installations and processes on our sites, record findings in our eQMS, and provide periodic reporting of these audits to management.Participate in conducting audits of technical phases carried out as part of regulatory studies, and provide support during audits of final reports in the event of increased activity.Represent Quality Assurance at our two sites, ensure the application of the quality policy defined by Management, provide quality support to staff, and deliver related training.Contribute to the design, deployment, and monitoring of the quality management system, as well as to updating quality documentation.This description includes the main responsibilities and is not exhaustive.The Profile We Are Looking ForYou have a BAC+2 (associate degree or equivalent) in qualityYou have mandatory experience in GLP/OECD (Good Laboratory Practice) of at least 2 years in a research laboratoryYou have at least a B2 level in EnglishYou are proficient in auditing technical documents and study reports, and you have the scientific knowledge needed to adapt quicklyYou are recognized for the following qualities: good organization, proactivity, rigor, team spirit, strong interpersonal skillsConditionsPermanent contract (CDI)Position based in Fontenay-lès-Briis (91) – 80%, with occasional travel to Paris – 20%Start date: as soon as possibleVeranex a souscrit au principe de l'égalité des chances et interdit toute forme de discrimination. Tous les candidats qualifiés seront pris en considération pour un emploi, sans distinction de race, de couleur, de religion ou de croyance, de sexe (y compris la grossesse, l'identité de genre ou l'expression de genre), d'orientation sexuelle, de statut parental ou marital, de handicap, d'âge, de statut d'ancien combattant protégé, d'origine, sociale ou ethnique, ou de toute autre caractéristique protégée par la loi.

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