Job Information
Zimmer Biomet Supplier Quality Engineer m/w - temp 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
As a Quality Supplier Engineer (m/w) you are responsible for Supplier Qualification, Supplier Change Notification, Supplier Corrective Action and Part / Service Qualification of all Quality Impacting Suppliers.
This position is a 2 years integration project mission.
How You Create Impact
Supplier Qualification / Requalification (encompassing audit and Supplier Quality Agreement).
Supplier Corrective Actions are to be completed on time to phase and must eliminate the reoccurrence of non-conformance.
Supplier Change Notification shall be conducted in partnership with RA (Regulatory Affairs), Development Engineering, Process Engineering, Research Engineering, Sourcing, and SME (Subject Matter Expert) if applicable.
Supplier Production Process Approval shall be implemented on time and to plan. Driving continuous improvement initiatives within the supplier base to enhance the quality, efficiency, and reliability of supplied components or services.
Supplier Performance shall be monitored and reported at the Quarterly Supplier Review Board.
Support the implementation of global procedures, work instructions and forms.
What Will Make You Stand Out
You hold a Bachelor's degree in technical, engineering, life sciences or any related field.
In addition you have a proven track record in supplier quality engineering within the medical devices industry, and you have gained experience as an ISO13485 Certified Lead Auditor.
What Will Make You Successful
Effectively communicating with internal teams, suppliers, and other stakeholders to resolve quality issues, implement changes, and ensure alignment with quality objectives.
Identifying and addressing root causes of quality issues through structured problem-solving methodologies
Evaluating and selecting suppliers, assessing their capabilities, and managing relationships to ensure consistent quality of supplied components or services.
Understanding and ensuring compliance with relevant regulations and standards such as ISO 13485, FDA regulations (e.g., 21 CFR Part 820), and other international regulatory requirements.
Conducting supplier audits to assess compliance with quality standards, identify areas for improvement, and ensure adherence to specifications.
Good computer skills, including Microsoft Office Suite.
French and English fluency.
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