Jesus Damian Monarrez Aguilera

Soy una persona trabajadora, organizada y responsable. Tengo más de cinco años de experiencia en calidad y procesos. También me considero una persona resolutiva, con liderazgo, capaz de resolver problemas y buscar
mejora continua

Sonoco
Quality Supervisor 
May 2022 - Oct 2024 

*Continuously improve and maintain the QMS aligned with the certifications and regulations required by customers. (ISO 9001/13485). 
*Conducted internal, corporative, client and supplier audits Lead and executed Six Sigma projects, applying DMAIC methodologies to improve operational efficiency and reduce defects. 
*Follow up and resolve CAPAs (corrective actions and preventive actions),using mehodologyes such as PDCA, Ishikawa, FMEA, 8D Method, 5 Whys. Developed and executed evaluation processes to select suppliers. 
*New model introduction validation (IQ,OQ,PQ). 
*Provide support to the internal area of manufacturing, quality, R&D, purchasing, to resolve problems that come from a supplier. Participate in KAIZEN with the other departments to solve company problems. 

Hisense Electronica de Mexico 
Quality Engineer 
Feb 2020 - May 2022

*Utilized statistical tools and data analysis to identify patterns, trends, and areas for improvement in quality processes. (Histogram, Scatter Plots, Pareto Analysis, Capability Indices, Statistical Process Control and Gage R&R). 
*Supervised and coordinated the incoming materialsinspection process, ensuringcompliance with technical specifications. 
*Lead validation projects from the planning phase through to implementation, ensuring timely Develop and implemented processes to assess the quality of incoming materials suppliers. 
*Implemented selection criteria and conducted supplier audits

Benchmark Electronics Jr. 
Process Quality Engineer 
Oct 2018 -Feb 2020

*Support projects to reduce cycle times, improving production capacity and minimizing labor costs. 
*Support on investigations into quality issues, identifying and addressing root causes to continually improve quality standards. 
*Collaborate on the training of staff on issues related to quality and good manufacturing practices. Support in the identification of non-conformities and in the implementation of corrective and preventive actions to eliminate the root causes of the identified problems. 
*Collaborate in the creation and maintenance of quality documentation, including manuals, procedures, instructions and records.

*CETYS Diploma in Medical Manufacturing Engineering- 2024 
*ASQ Six Sigma Green Belt - 2023 
*CANACINTRA ISO 9001:2015 Leader Auditor - 2023/2024 
*Universidad Autónoma de Baja California Industrial Engineering - 2015-2020