Quality Operation
il y a 1 jour
locations- Louvain-la-Neuve- time type- Full time- posted on- Posted Today- job requisition id- JR00014604- Zoetis est le leader mondial de la santé animale, voué à accompagner ses clients et leurs entreprises. S'appuyant sur plus de 70 ans d'expérience en santé animale, Zoetis découvre, développe, fabrique et commercialise des vaccins et des médicaments vétérinaires, complétés par des produits de diagnostic et des tests génétiques, ainsi que par une gamme de services. Zoetis est au service des vétérinaires, des éleveurs d’animaux de rente et de ceux qui élèvent et prennent soin des animaux de compagnie et de rente, avec la vente de ses produits dans plus de 100 pays. - Zoetis compte environ 11.000 collègues qui soutiennent nos activités dans les domaines des ventes, de la recherche et du développement, de la fabrication et de diverses fonctions mondiales. Lorsque vous rejoindrez Zoetis, vous aurez l’opportunité d’apprendre, de développer vos compétences et d’enrichir votre carrière de nombreuses manières : formation sur le terrain, travail sur des projets ambitieux ou simple apprentissage entre pairs et managers. Nous bâtissons notre prochaine génération de leaders en investissant dans le développement de nos collègues. - Zoetis is an American drug company, the world's largest producer of medicine and vaccinations for pets and livestock. - The Zoetis Louvain-la-Neuve site is specialized in the aseptic manufacturing of vaccines, monoclonal antibodies, antibiotics and hormonal product for pets as well as livestock animals. - Position summary - The job consists in the release of veterinary medicinal products and intermediate products in compliance to the marketing authorization and within relevant cGMP/GDP guidelines. This includes the review and approval of the master batch instructions in compliance with the validation data. - You will work in close cooperation with the manufacturing dept by providing quality oversight and floor support including GMP guidance for manufacturing operations. - As part of a very diversified job, you will also be in charge of: - Follow up on quality incidents, defines and follows up on CAPA’s in order to optimize overall performance and to minimize adverse impact on Zoetis products.- - Coordination of investigation linked to quality incidents or capability improvements for finished product- - Management of complaints coming from external customer- - Communication with the distribution centre and with Zoetis Global supply chain dept- - Creation and maintenance of quality procedures- - Attendance as QA representative in project linked to the manufacture of new products- - Attendance as QA representative in audits performed by FAMHP, USDA, FDA or external customers.- You will be part of the quality team, and you will enjoy a high degree of independence. - Requirements - BS Degree in science related field - >3 years of experience in pharma health industry and preferably in a release/QA position - Knowledge of cGMP - Proven ability to work cross-functionally with other departments as well as independently - Ability to manage multiple projects simultaneously and prioritize work, goals and tasks Proficiency in English and French - Quality oriented - Why would you join the Quality Team? - You will join a fast-growing company that has become the international market leader in the veterinary vaccine/pharmaceutical product. - You will benefit from a great autonomy in your work, with plenty of room for initiative, challenges and possibility to take ownership of your work. Full time
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Operations Engineer
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QA Batch Record
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QA Batch Record
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QA Batch Record
il y a 1 semaine
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