Location
Mexico
Job Type
Full-time
Posted
June 20, 2026
Job Description
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
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Submit your application for Sr Quality Release Engineer - Queretaro Site at Abbott
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