Quality Engineer II
Cartago, Cartago, Costa RicaJobPosted 1w agoStill listed 1w ago
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Job overview
The Quality Engineer II supports the Quality Management System for new and existing medical devices, ensuring regulatory compliance and high quality standards. The role analyzes quality data, investigates nonconformances, identifies root causes, and drives corrective and preventive actions while collaborating with cross‑functional teams on continuous improvement and product/process validation.
Skills & qualifications
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Full job description
Summary The Quality Engineer II supports Quality Management System (QMS) activities for new and existing products, manufacturing processes, and quality controls to ensure compliance with regulatory requirements and quality standards. This role analyzes quality data, investigates nonconformances, identifies root causes, and drives corrective and preventive actions to improve product and process performance. Working closely with cross-functional teams, the Quality Engineer II contributes to continuous improvement initiatives, supports product and process validations, and helps ensure the delivery of safe, effective, and high-quality medical devices.
Qualifications Requires a bachelor’s degree in engineering or a related field,
3+ years of experience in quality engineering.
Proficiency in English.
Requires familiarity with QSR, ISO, and other applicable regulations and laws.
Manufacturing experience.
Medical device industry experience.
Demonstrates excellent verbal, written, and interpersonal communication skills.
Proficiency in MS Word, Excel, and PowerPoint.
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