Quality Engineer IV

About the role

The Quality Engineer IV will work at Abbott's Coyol Free Zone location within the Vascular Division, supporting the manufacturing of innovative, minimally invasive vascular products. The role combines scientific, engineering, and analytical expertise to ensure the highest quality standards for both new and existing devices.

Key responsibilities

• Apply quality principles, analyze quality records, prepare reports and recommend improvements.
• Conduct inspection, verification, and validation of components and materials used in development processes.
• Identify and address recurring quality or testing reliability problems.
• Document quality issues and performance metrics for management review.
• Interface with internal teams and external partners to resolve quality concerns.
• Plan and execute high‑level projects, including investigations, equipment assessments, and process improvements.
• Anticipate future trends, benchmark internally and externally, and prepare proactive action plans.
• Investigate, test, gather data, perform preliminary analysis, and communicate findings and recommendations.

Required profile

• Bachelor’s degree in engineering, science, or a closely related discipline, or equivalent technical experience.
• Minimum 4 years of experience in the medical device or related industry.
• Intermediate English proficiency (B1 level).
• Quality background with knowledge of FDA and ISO regulations is desired.
• Relevant certifications such as CQE, CQA, Lean, or Six Sigma are preferred.

Required skills

• FDA/ISO regulation knowledge
• Lean methodology
• Six Sigma principles
• Statistical analysis
• Quality engineering techniques

What we offer

• Career development opportunities within a global healthcare leader.
• Recognition as a great place to work and a commitment to diversity and inclusion.
• Access to international growth pathways and professional training.