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Zimmer Biomet Quality Engineer / Quality Supplier Engineer m/f in Toulouse, France

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered, and recognized.

What You Can Expect

This role entails participating with projects on a global level, with a specific focus on the Quality Systems integration of newly acquired sites in alignment with Zimmer Biomet Quality Management System. General expectations are to ensure implementation of, and compliance, to applicable QMS processes, tools and procedures, and work with cross-functional departments, sites, suppliers, and experts within and outside Zimmer Biomet in order to ensure the assigned project activities are complete. This position also includes coordinating and supporting the Quality Management Processes, including but not limited to, Supplier Quality Management, Supplier Audits, Corrective and Preventive Action and Validation in order to communicate and implement Zimmer Biomet Quality Objectives.

How You'll Create Impact

  • Coordinating corporate supplier quality systems projects for the development and implementation of processes, procedures and instruction to sustain and improve the Supplier Quality Management System.

  • Supporting top management in the strategic planning of quality systems strategies and objectives.

  • Coordinating with cross-functional and cross-divisional teams in the development and implementation of corporate quality systems strategies and objectives.

  • Coordinating corporate quality systems initiatives for the development & implementation of harmonized supplier quality systems, best practices across the organization.

  • Identifying and solving continuous improvement opportunities for the improvement and increased efficiency of Zimmer’s quality systems.

  • Identifying and solving product, system and process problems.

  • Supporting various groups as needed for conducting audits and assessments of internal processes and suppliers manufacturing sites, CAPA etc.

What Makes You Stand Out

  • Ability to coordinate day-to-day operational aspects of a Supplier Quality Systems projects and scope.

  • Ability to create and execute project work plans and revise as appropriate to meet changing needs and requirements.

  • Familiar with all aspects and elements of a quality system including but not limited to purchasing controls, management responsibility, resource management, product realization and measurement, analysis and improvement processes.

  • Knowledge on aspects of quality assurance techniques such as: inspection methods, statistical sampling plans, gauging and test methods concepts, validation, and statistical process control

  • Effective application of Quality Systems methodology and project standards.

  • Ability to harmonize and effectively implement best practices for supply chain management, supplier quality and purchasing controls world-wide.

  • Technical expertise, project management and time management skills.

  • Ownership for the commitment to continuous improvement.

  • Ability to work independently and consider options for completing work.

  • Strong written and verbal communication skills.

  • Demonstrated willingness to independently identify, learn and apply new skills as needed for completing tasks.

Your Background

  • Must have at least a Bachelor’s degree

  • Bachelor’s degree in Engineering

  • Technical, engineering, and/or scientific background is strongly preferred.

  • 3-5 years of experience in Quality/Regulatory Compliance field is preferred

  • 3-5 years of experience in Project Management is preferred

  • Must be familiar with Microsoft Office Suite.

  • Familiarity with tools such as Windchill, EtQ, SAP etc. are an advantage

Who We Are

VIMS, recently acquired by Zimmer Biomet Holdings, Inc. specializes in developing and commercializing visualization systems for laparoscopic and arthroscopic procedures, offering fully integrated broadcasting solutions and 6K-7K ultra-high-definition resolution.

EOE/M/F/Vet/Disability

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