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INTERNSHIP SCOPE The Quality Engineering Intern will be supporting critical programs related to monitoring and follow up corrective actions for the incoming inspection area. The Intern will have high exposure to multidisciplinary teamwork and relationships. This role will develop and implement best practices focused on preventing defects, reducing variations, and driving continuous improvement to meet protocols. EXPOSURE TO THE FOLLOWING RESPONSIBILITIES Validate compliance with ISO 13485 y 21CFR 820 quality system regulations. Analyze, review, and implement new processes that contribute to the improvement of the QMS. Document SGC and GxP control activities with mentoring from other team members. Draft and update supplier documentation through the change order process (CO-ASL) to proactively comply with applicable internal and external standards and regulations. Requirements Advanced university studies in engineering or life sciences. Demonstrate interest in career development in medical devices. Basic understanding of manufacturing, quality and engineering processes in a highly regulated industry, such as medical device, pharmaceutical, aerospace, automotive, etc. Basic computer skills required (AutoCAD desirable) Intermediate-advanced English level Benefits Interns will receive a subsidy package to support expenses such as transportantion, meals, equipment among others.