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Quality Engineering

Location:
San Antonio, TX
Posted:
June 03, 2016

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Resume:

Janay Becerril Escamilla

**** ******* *** *** *******, TX 78258 210-***-**** acu2wm@r.postjobfree.com mx.linkedin.com/in/becerriljanay

Quality Management Process Engineering Project Engineering

Highly skilled professional with bi-lingual and multi-cultural experience and with an emphasis in multinational manufacturing companies – molding, assembly & packaging.

A well-motivated individual who stands ready to assume any position of responsibility, and self-starter who is able to work in a fast-paced environment within the European, American and Hispanic cultures.

Quality Assurance Systems

Loss Elimination Strategies

Cross-functional Collaboration

Manufacturing Operations

High Productivity with Collaborative Approachability

Project Management

Cost Reduction

Injection Molding

High Performance Organization

Process Improvement

Professional Experience

PROCTER & GAMBLE MEXICO Estado de Mexico, Mexico December, 2008 – January, 2016

Multinational consumer goods Company with $8B in sales and 65 brands.

Materials, Process and Delivery Expert (2015 -2016)

Responsible for savings projects through raw and pack material changes and material specification’s maintenance for Manual and Power Oral Care brushes and dental floss for North America, Eastern European, Middle East, Asian and Latin American markets.

Cost reduction:

oDelivered $800M USD of savings by designing and implementing a refined inter-plant inventory transfer process, utilizing aged materials in other plants to ramp-up production in Mexico. Various SAP ERP design models were used to execute a material qualification plan involving the Manaus Plant in Brazil, and Manual Oral Care area in Alce Blanco Plant in Mexico.

oDeveloped a material qualification plan and experimental test parameters for plastic resins change valued on 1.2M USD in savings.

oExecuted and achieved successful results using material test parameters on three separate packing lines for a PVC to PET material change project on manual Oral Care.

Materials Specification Maintenance:

oMaintained the Incoming Inspection System, focused on plastic resins and electrical components:

Reviewed and aligned specifications with Research and Development departments located in Europe, assuring that critical characteristics of the materials were met and verified.

Verified compliance of suppliers, system quality requirements, and technical specifications of materials through the Certificate of Analysis initiative.

Managed the communication system and communication with suppliers.

oDeveloped 24 packing specifications for a new initiative which included artwork changes, involving 11 finished goods for dental floss and equipment replacement for manual Oral Care products.

Quality Area Leader for Manual and Power Oral Care (2010 – 2014)

Responsible for bristling, assembly and packaging quality system for Manual and Power Oral Care in North American & Latin American markets.

Quality Assurance Systems for Manual and Power Oral Care

oAwarded with the “Quality Promise Award” on the Health Care Category as a result of the work developed for regulations compliance consisting of:

Developed the inspection plan for finished goods for manual toothbrushes with Research and Development organization, QA Global Innovation, QA Go to Market and brushing plants: Iowa City, Newbridge and Manaus plants.

Established an inspection plan for finished goods for power toothbrushes with Research and Development organization, QA Global Innovation, QA Go to Market and Marktheidenfeld brushing plant.

Improved Process Capability from 60% to 85% on end-rounding (classified as consumer critical parameter).

Trained and certified the quality analyst’s group and progressive maintenance personnel on end-rounding test.

Developed, trained and implemented the complete staff in Manual Oral Care in the renewed process control strategy for the bristling process.

Implemented quality inspection logbooks.

oDesigned and Implemented the Device Master Record System involving work-in-process product release, records management and finished product release on manual and power Oral Care and dental floss areas.

oSimplified the material verification process and traceability using SAP System.

oSimplified the number of quality standards from 230 to 6 in manual and power toothbrushes, increasing quality analysts’ capability.

oAccountable for the quality System on manual and power toothbrushes, representing 50% of the plant organization, achieving zero critical observations and zero repetitive major observations on internal and external audits: ISO 9001, ISO 13485, FDA, UL, VDE (power toothbrushes) and Mexican Board of Health.

oResponsible for the corrective actions and preventive actions for manual and power Oral Care keeping 100% of action plans on track.

oAuthored and maintained the following standard operating procedures: Laboratory Controls, Goods Manufacturing Practices, Line Clearance and Documentation.

oManaged 28 people.

Quality Engineer for Manual Toothbrushes (2008 – 2010)

Responsible for bristling and packaging quality system for manual Oral Care throughout Latin America.

Loss Elimination Strategies and Quality System

oImproved quality capability from 52% to 80% by solving critical and major observations related to:

Developed and implemented the validation System, creating a validation model across the site (critical repetitive observation).

Implemented 3M audits – mislabel, miscode and mismatch to eliminate major observations.

Lead loss elimination events to improve process capability on brushing and packing processes.

oResponsible for consumer complaints for Manual Oral Care keeping 100% of action plans on track.

Education

B.SC. Industrial Engineering

INSTITUTO POLITECNICO NACIONAL – UPIICSA

Mexico City, Mexico

Statistical Process Control Postgraduate

INSTITUTO POLITECNICO NACIONAL – UPIICSA

Mexico City, Mexico

Leadership Training

• Corrective Actions Preventive Actions (CAPA) Bootcamp training

• Basic Trackwise Training

• Nom-241-SSA1-2012 Good manufacturing practices for facilities dedicated to manufacturing of medical devices

• ISO 9001:2008 & 13485:2003

Language Expertise

Spanish, Native

English, Fluent



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