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 11000 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.
Mission
As part of the Quality department and acting as team leader, you will organize the release of unlabeled vaccines/monoclonal antibodies/pharmaceutical products purchased and/or manufactured by Zoetis Belgium sa Louvain-la-Neuve in compliance with the requirements of the registration dossier/marketing authorizations and guidelines of Good Manufacturing Practices.
Key accountabilities
The job consists in:
* Ensuring the leadership of the team including decision-making, coaching, mentoring, developing the team’s skills.
* Acting as Deputy Qualified Person.
* Organizing the review and approval of executed manufacturing batch records.
* Providing quality oversight and floor support including GMP guidance for manufacturing operations.
* Ensuring the review and approval of Manufacturing and Laboratory investigation including CAPA's implementation.
* Managing customer complaints.
* Overseeing the management of Product Quality Review process.
* Acting as a key quality operations liaison between functional departments in Production, Quality and Supply Chain.
* Driving continuous improvement initiatives which positively impact cycle time, productivity, efficiency and quality of work through lean methodology.
Who are we looking for?
* At least 5 years of experience in a pharmaceutical industry.
* QP registration number (AFMPS) and a first experience as QP.
* Knowledge in guidance needed for QP release.
* Quality-oriented and rigorous mind with a high level of flexibility.
* Ability to manage priorities, to plan and coordinate different activities.
* Good communication skills (oral and written).
* Fluent in French; full professional proficiency in English.
* Knowledge in electronic batch record is an asset.
Why would you join the Quality Team?
You will join a fast-growing company that has become the international market leader in the vaccines/monoclonal antibodies/pharmaceutical products.
You will benefit from a great autonomy in your work, with initiatives, challenges and possibility to take ownership of your work.
Full time
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