Equipment and CSV QC Coordinator/TL

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.

Cette nouvelle opportunité au sein de Zoetis est pour vous !

Position summary
The Equipment and CSV QC Coordinator/TL coordinates and actively contributes to the qualification and maintenance of laboratory equipment, leads Computer System Validation (CSV) activities, and manages, supports and coordinates a team of equipment and digitalization specialists. The role also includes strong involvement in projects for the implementation of digital tools in the QC lab, such as digital scheduling systems and Laboratory Execution Systems (LES). This role supports laboratory operations, drives continuous improvement, ensures data integrity within the QC environment, and ensures compliance with regulatory standards.
Main responsibilities
• Maintain all QC laboratory equipment, ensuring proper calibration, qualification, and preventive maintenance according to schedule.
• Oversee and actively participate to troubleshooting and resolution of equipment-related issues to minimize downtime and ensure uninterrupted laboratory operations.
• Lead Computer System Validation (CSV) activities for laboratory instruments and software, ensuring compliance with GMP, FDA, and other relevant regulations.
• Implement CAPEX Master Plan for QC equipment and highlight and anticipate obsolescence and replacement needs for both equipment and software.
• Coordinate equipment installations, upgrades, and decommissioning in collaboration with vendors and internal stakeholders.
• Develop, review, and approve equipment qualification protocols, validation plans, and related documentation.
• Train laboratory staff on equipment use, maintenance procedures, and CSV requirements.
• Monitor and report key performance indicators (KPIs) related to equipment reliability, validation status, and compliance.
• Ensure data integrity and security of electronic records generated by laboratory systems.
• Participate in audits and inspections, providing expertise on equipment and CSV topics.
• Lead and supervise projects for the implementation of digital tools in the QC lab, such as digital scheduling systems and Laboratory Execution Systems (LES), ensuring successful deployment, user training, and continuous improvement.
• Supervise, manage, and coordinate a team of equipment specialists, fostering their development and ensuring effective team performance.
• Drive continuous improvement initiatives to optimize laboratory efficiency and compliance.
Education and experience
• Master’s degree in Life Sciences, Engineering, or related field.
• Proven experience in QC laboratory equipment management and Computer System Validation (CSV) within a regulated environment (pharmaceutical, biotechnology, or similar industry).
• Experience in team management or supervision is a plus.
Technical skills and competencies
Strong knowledge of GMP, FDA, and other relevant regulatory requirements.
Excellent organizational, problem-solving, and communication skills.
Ability to lead projects and work collaboratively in cross-functional teams.
Fluent in English (written and spoken) 
Working Language French
Experience with electronic data management is highly desirable.

Notre offre:
Vous ferez partie d'un environnement de travail international avec de la place pour l’ownership et le développement personnel.
Nous offrons un excellent package de rémunération (chèques-repas, écochèques, frais de déplacements, package assurances et Fonds de pension…)
Un équilibre vie privée et vie professionnelle 

Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.

Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.