Ingénieur Qualité; H​/F - Dispositifs Médicaux

Job Title

Chez Zimmer Biomet, nous croyons qu'il faut repousser les limites de l'innovation et faire avancer notre mission. En tant que leader mondial de la technologie médicale depuis près de 100 ans, la mobilité d'un patient est améliorée par un produit ou une technologie Zimmer Biomet toutes les 8 secondes. En tant que membre de l'équipe Zimmer Biomet, vous partagerez notre engagement à fournir mobilité et vie renouvelée aux personnes du monde entier.

Pour soutenir notre équipe de talents, nous nous concentrons sur les opportunités de développement, les groupes de res sources d'employés (ERG) solides, un environnement de travail flexible, des récompenses totales compétitives spécifiques au site, des incitations au bien-être et une culture de reconnaissance et de récompenses de performance. Nous nous engageons à créer un environnement où chaque membre de l'équipe se sent inclus, respecté, responsabilisé et reconnu.

VIMS is a company based in Villeneuve-les-Bouloc (31), recently integrated into the international group ZIMMER BIOMET. The company develops, manufactures, and markets gainable videoscopy solutions (medical-surgical equipment) to clinics and hospitals in France and internationally. It synergizes with the visualization systems of implants and equipment dedicated to arthroscopy.

At our production site in Villeneuve-les-Bouloc, you ensure the implementation and organization of quality activities. You ensure the application of the Quality Management System (QMS) requirements and guarantee the respect of the quality procedures in force.

• Contribute to the maintenance and continuous improvement of the production site's Quality Management System (QMS).
• Participate in change management (Change Control) and support teams in their implementation.
• Prepare and support external audits as a quality expert (SME), ensuring the coordination of associated activities.
• Lead non-conformities, investigations, and corrective/preventive actions (CAPA) via the ETQ quality system.
• Manage the procedures for blocking, vigilance, and product recall to ensure patient safety and regulatory compliance.
• Ensure the writing, updating, and management of quality documentation and associated data in place systems.
• Coordinate technical evaluations of customer complaints and participate in supplier qualifications in collaboration with concerned teams.

• Master's degree in medical devices, pharmaceutical industry with a quality specialization, or engineering degree with a quality specialization.
• Significant experience in a quality function within the medical industry.

• Good mastery of the documentary management of a Quality Management System.
• Knowledge of problem-solving methodologies and associated quality tools.
• Knowledge of medical device sector standards and regulations, including ISO 13485 and Regulation (EU) 2017/745 (MDR).
• Experience with quality management software (ETQ or equivalent).
• Professional proficiency in French and English, both written and spoken.
• Strong team spirit, organizational skills, and ability to work across different services.

Then apply online by sending your application dossier on our website. We look forward to receiving your application!

For more information about us, visit (Use the "Apply for this Job" box below)..fr

EOE/M/F/Vet/Disability