Job Information
Zimmer Biomet Supplier Quality Assurance Administrator in Remote, Poland
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
Supplier Quality assurance Administrator position is responsible for timely completion of supplier qualifications for the EMEA region supplier base. The tasks include: initiating qualification records within the electronic system, obtaining required documentation from the suppliers and assessment of the documentation provided. The role involves interaction with internal and external stakeholders
How You'll Create Impact
Communication with suppliers to obtain the required documentation in compliance with documented procedures.
Compiling Supplier documentation required based on the qualification type and supplier risk category.
Review and assessment of the supplier documentation obtained.
Review of the shared supplier list and coordinate the assignment of the site to conduct the main qualification and audit.
Initiation and evaluation of new supplier qualifications, periodic supplier requalification, status changes using electronic system.
Liaising and supporting internal stakeholders with all tasks associated with supplier qualification process.
Support in the administration of the audit schedule.
Coordination of the supplier audit meetings.
Manage data entry, maintenance of supplier documentation and tracking of upcoming qualifications to ensure qualifications are completed on time and in compliance with documented procedures
Preparation of supplier performance monitoring data required to fulfill the supplier qualification requirements.
Maintenance of supplier ISO certificates in the electronic system
What Makes You Stand Out
English language skills (fluency in reading, writing, listening, and speaking).
Strong writing and communication skills.
Responsible, professional, detail oriented.
Strong computer skills
Your Background
Bachelor’s Degree in life sciences, technical (engineering), medical sciences.
Experience of working within medical device environment preferred.
Understanding of ISO 13485:2016 requirements preferred.
EOE/M/F/Vet/Disability