Descripción y detalle de las actividades
Appraise supplier credentials, agreements and survey responses
Route new supplier requests for approvals
Work with suppliers to communicate requirements and establish process controls in alignment with Engineering, Manufacturing, Quality and Business Objectives
Perform reviews with suppliers to determine manufacturability of components
Participate in the development of quality requirements for purchased component/assemblies
Review and develop risk mitigation controls for supplied parts
Assist suppliers with investigation and process improvement initiatives
Perform supplier audits (quality system, process and product audits)
Create supplier performance metrics and report on performance to suppliers and management.
Ensure alignment of supplier quality metrics with business objectives
Disposition nonconforming materials and initiate follow up activities to ensure proper corrective action and preclude recurrence of rejections.




Work with various engineering disciplines to resolve customer return issues related to supplier quality.
Work with incoming inspection to ensure proper part surveillance.
Review and approve first articles on custom fabricated components.

Experiencia y requisitos
Minimum of three years' experience in quality engineering and/or supplier management, preferably in the medical device industry.
Knowledge of manufacturing processes, procedures and production equipment.
Auditing experience and training (ASQ-Certified Quality Auditor and or Lead Auditor Training for ISO *****)
Advanced English (spoken and written) – Essential
Familiarity with Quality Standards (ISO *****, ISO ****, FDA QSR, etc.)
Demonstrated knowledge and experience with risk analysis, statistics and quality tools.
Experience with PCBs, cables, circuit boards, and circuit board assemblies
Strong problem solving ability;
Strong Analytical Skills;

Beneficios
Incentivos superiores a LFT

📌 Supplier Quality Engineer (Mexicali)
🏢 Masimo
📍 Mexicali