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
Ready to Apply?
Submit your application today and join our talented team at Abbott.
Submit ApplicationJob Details
- Location Mexico, Querétaro
- Job Type Full-time
- Category Engineers
- Posted Date June 19, 2026
- Application Deadline July 29, 2026