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 talented 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 inspired, invested, cared for, valued, and have a strong sense of belonging.

What You Can Expect

This Supplier Quality Assurance Administrator is responsible for timely planning and completion of supplier audits for the EMEA region. The role involves interaction with internal and external stakeholders to ensure supplier audits are scheduled and completed on time, including required follow ups and resource assignment. This position requires strong understanding of medical device industry requirements and significant auditing experience (ISO 13485:2016 Lead auditor qualification – required).

How You'll Create Impact Creation and maintenance of the supplier audit schedule for the EMEA region.Planning and conducting the audits in line with the defined requirements.Compiling supplier audit reports within set timeline.Facilitate training of newly trained auditors.Compiling Supplier documentation required based on the qualification type and supplier risk category.Coordination of SCARs raised from supplier audits.Provide input into the metrics review meeting, ensuring any issues related to supplier audits are raised and addressed.Preparation of supplier performance monitoring data required to fulfill the supplier qualification requirements.Maintenance of supplier ISO certificates in the electronic system.Support site supplier quality teams with PMML, SCNs and DRMs.What Makes You Stand Out English language skills (fluency in reading, writing, listening, and speaking).Strong writing and communication skills.High level of accuracyResponsible, professional, detail oriented.Strong computer skills.Your Background Bachelor’s Degree in life sciences, technical (engineering), medical sciences – requiredExperience of working within medical device environment (minimum 2 years) – requiredSignificant auditing experience – requiredSupplier audit experience  - requiredISO 13485:2016 Lead auditor qualification – requiredUnderstanding of MDR requirements – requiredUnderstanding of other ISO standards including  ISO/IEC 17025 and ISO 11135 - preferred.   Travel Expectations

EOE/M/F/Vet/Disability