Abbott is seeking a Sr.
Quality Engineer at the Querétaro site to sustain quality systems and lead validation activities for medical devices.You will work with Manufacturing, Engineering & Regulatory teams to ensure compliance and KPI achievement, driving continuous improvement.
The role requires 3–5 years in quality engineering within the medical devices or pharma sectors, with experience in CAPAs, NCMR, audits, and strong knowledge of FDA/GMP/ISO ***** standards.
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📌 Senior Quality Engineer & Process Validation Leader (Santiago de Querétaro)
🏢 Abbott
📍 Santiago de Querétaro
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