Job Information
Zimmer Biomet Supplier Quality Assurance Lead Auditor (ISO 13485:2016) in Remote, United Kingdom
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 GBS position 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 accuracy
Responsible, professional, detail oriented.
Strong computer skills.
Your Background
Bachelor’s Degree in life sciences, technical (engineering), medical sciences – required
Experience of working within medical device environment (minimum 2 years) – required
Significant auditing experience – required
Supplier audit experience - required
ISO 13485:2016 Lead auditor qualification – required
Understanding of MDR requirements – required
Understanding of other ISO standards including ISO/IEC 17025 and ISO 11135 - preferred.
Travel Expectations
- Up to 30%
EOE/M/F/Vet/Disability