GMT Products

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.

The goal of this function is to support the implementation of the projects & the improvements related to production processes topics into our GMP manufacturing facilities.

We are looking for a collaborator who is passionate about their work and eager to take on a challenge.

Job Description

• Support “Products and Processes Technical Support Sr. Mgr” & GMT Project Managers for technical aspects in New Products introduction, Product Transfers projects & improvement or problem resolution projects.
• Provide technical support, including resolution of technical issues, assisting in the identification of root causes, developing recommendations, and supporting implementations (production investigations with repeated occurrences and associated with technical issues).
• Follow up of QC results, trend & capability analysis for projects managed by GMT P&P technical support.
• Share & identify CPP and CQA to support validation process.
• Redaction of technical documents & participate in the interpretation of validation results if needed.
• Participate in the review and approval of internal documents such as monographies describing new processes.
• Ensure that the processes remain under control.
• Participate in technical training/development (coaching) of production members (operators included).
• Stay up to date regarding technical aspects related to the value stream and ensure a technological watch.

Qualifications

Education and experience:

University degree in appropriate discipline (i.e., pharmacy, biology, microbiology, engineering, or other scientific discipline).

3 years of relevant experience in the pharmaceutical/biotechnology industry.

Technical skills and soft skills competencies:

• Practical and effective knowledge of main engineering and pharmaceutical technics (production processes).
• Strong knowledge in cells culture, antigens, vaccines and/or biopharmaceuticals manufacturing.
• Knowledge of GMP principles.
• Strong integrity and motivation.
• Resilient and ready for change.
• Quality-oriented and rigorous mind with a high level of flexibility.
• Ability to manage priorities, to plan and coordinate different activities.
• Strong organizational and communication skills and a demonstrated ability to work in a culturally diverse, cross-functional workplace.
• Strong commitment to customer service, and continuous improvement.
• Demonstrated excellent English and French knowledge (oral and written).

Why would you join the GMT 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.