Quality Assurance Specialist

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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.

Interested in end-to-end vaccines and other injectable drug products manufacturing process?
Looking for a more diversified activities challenge?
It’s time to expand your area of expertise!

Join the Team and become the swiss knives of the Quality Operation Department by supporting our Manufacturing, Engineering, Packaging and Quality controls departments.

Mission

Member of the Quality department, you ensure QA oversight of a wide range of non-batch related topics across the end-to-end vaccines manufacturing processes such as equipment qualification, change management, deviations, trends monitoring and improvement projects.

Next to these supportive activities, you will also work on structural project to strengthen our systems and ensure compliance with Corporate Quality Guidelines.

Key accountabilities

Prepare and participate to regulatory inspections, including CAPA management.

Lead and execute the Data Integrity Plan.

Plan, lead and report on internal audits.

Design and improveprocesses following Corporate Quality Guidelines.

Provide the QA oversight for selected qualification / validation activities (HVAC, Sterilizers, Temperature controlled areas…).

Support quality operations to ensure quality related commitments (CAPAs, change management, deviations) are handled in a timely manner.

Maintain Site Support Documentation (e.g., Contamination Control Strategy, Site Master File);

Conduct periodic trending analysis of quality systems performance.

Bring support to develop and/or report quality performance metrics.

Who are we looking for?

Excellent effective understanding of EU GMP and FDA cGMP; able to find pragmatic solutions to implement requirements in operations.

University degree in a Science or Engineering discipline (e.g., Pharmacy, veterinary or Biological engineering).

5+ years of experiences in the sterile pharmaceutical industry, in a QA or production environment.

Experienced in managing internal audits.

Proficient in pharmaceutical quality management systems (e.g., deviations, CAPA and change control).

Knowledge of Data Integrity requirements, both for hard copies and computerized systems

Good communication skills (oral and written).

Fluent in French; full professional proficiency in English.

Why would you join the Quality Team?

You will join a fast-growing company that has become the international market leader with a corporate culture heritage from Pfizer.

By your unique background, experiences, knowledges, skills, and ideas, you will bring your stone to building an ever-stronger Quality organization.

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.