Posted:
June 14, 2026
Location:
Tijuana, Baja California, Mexico

Job Description

Work Flexibility: Onsite

What You Will Do

This role is accountable for building, maintaining, and continuously improving a Quality Management System that meets global medical device regulatory requirements. As a Senior Specialist, you will guide QMS development and execution across the organization, ensuring regulatory readiness, audit compliance, and alignment with corporate quality standards.

  • Ensure Quality Management System (QMS) compliance with applicable internal and external regulatory requirements, including site, corporate, FDA, ISO, EU MDR, and country‑specific regulations.

  • Develop, implement, and control updates to regional and local quality management system processes aligned with corporate and divisional QMS requirements.

  • Support the management and coordination of internal and external audits, including preparation, execution, and follow‑up activities.

  • Coordinate and lead Management Review f...

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    Job Overview

    Job Type: Full time
    Location: Tijuana, Mexico
    Posted: June 14, 2026
    Deadline: July 24, 2026