About the Role
The Opportunity
This role ensures that all medical devices are released in full compliance with applicable regulatory requirements (ISO 13485, 21 CFR Part 820, NOM-241), internal procedures, and customer specifications. The individual oversees the documentation review process, manages the Quality Release team, drives continuous improvement initiatives, and serves as the primary decision-maker for nonconformities related to final product documentation.
What You’ll Do
Ready to Apply?
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