Francs

Programa para adultos (16 aos en adelante)

Duracin: cuatro (4) niveles bsicos, dos (2) niveles intermedio y dos (2)
niveles avanzados.

Modalidad: regular (4 horas semanales), intensivo: (10 horas semanales) y

sper intensivo: (12 horas semanales).

Dirigido a

A directivos de alto nivel, con formacin profesional diversa y experiencia en gestin, que estn interesados en
adquirir y/o mejorar sus habilidades directivas y competencias en gestin. Los diferentes mdulos del programa
estn orientados a fomentar el desarrollo de habilidades directivas y competencias de gestin, a travs del
estudio y realizacin de proyectos multidisciplinarios, de intervencin en empresas, lo cual les permitir
adquirir una visin integral de la organizacin, acorde con la realidad actual.

Perfil del Ingresante

Poseer un ttulo universitario, de grado de licenciatura o su equivalente

Haber obtenido una calificacin promedio acumulativa de no menos de 3.0/4.0

Tener experiencia profesional pertinente, en posiciones gerenciales de, al menos 4 aos, para aquellos con
grado de licenciatura o su equivalente. Para solicitantes con postgrados o maestras, se exige una experiencia
mnima de 3 aos.

Perfil del Egresado

El egresado de Maestra en Administracin de Negocios de la Escuela de Gestin de la Universidad de Quebec

en Montreal (UQAM) & UNAPEC debe estar en capacidad de:

Liderar y gestionar empresas inmensas en entornos globales, competitivos y dinmicos habr obtenido una
slida formacin terica y metodolgica en las reas administrativas y de gestin, y habr desarrollado una
gran capacidad de reflexin que le permitir abordar con xito las diferentes problemticas que se presenten en
su entorno laboral, tomar decisiones estratgicas para su empresa u organizacin e implementar las acciones
necesarias para fomentar el bienestar general.

Participar en espacios acadmicos de discusin y anlisis y desempearse como profesionales

investigadores de las Ciencias Administrativas, porque habr desarrollado capacidad de anlisis y de
investigacin.

Establecer las directrices y las estrategias de negocios tendentes a posicionar a su empresa y sus productos
dentro del mercado global.

Valorar y entender los fenmenos que inciden en el desarrollo de la actividad empresarial.

Conocer los derechos y obligaciones establecidos en la legislacin nacional.

 Estar consciente de su responsabilidad en el proceso del desarrollo social y econmico del pas.

Desarrollar sus actividades empresariales apoyadas por principios ticos y responsabilidad social.

Requisitos de Admisin
Si es egresado de una universidad en Repblica Dominicana:

1. Acta de nacimiento legalizada

2. Certificacin de grado legalizada por el MESCYT
3. Rcord de notas universitario legalizado por el MESCYT
4. Curriculum vitae, sin anexos
5. Certificacin mdica oficial debidamente firmada y sellada
6. Tres (3) fotografas 22
7. Fotocopia de la cdula de identidad y electoral

Si es egresado de una universidad en el extranjero debe adicionar a todo lo anterior:

Fotocopia del ttulo de los estudios del Nivel de grado apostillado/legalizado. (Sustituye
el punto 2 de los requisitos arriba citados)
Rcord de notas apostillado/legalizado donde realiz sus estudios y por el Ministerio de
Educacin de Educacin Superior Ciencias y Tecnologa (MESCYT). (Sustituye el
punto 3 de los requisitos arriba citados)
Si es extranjero debe adicionar a todo lo anterior:

Fotocopia del pasaporte y visa de estudiante o cdula de residente dominicano

Si es egresado de UNAPEC:

Certificacin de grado legalizada por el MESCYT

Rcord de notas universitario legalizado por el MESCYT
Curriculum vitae, sin anexos
Certificacin mdica oficial debidamente firmada y sellada
1 fotografa 22

CAPA and Complaint Engineer II
Nombre de la empresaBaxter International Inc.
Fechas de empleomay. de 2017 actualidad

Duracin del empleo4 meses

UbicacinParque Industrial Itabo

Collaborate with the preparation and realization of the metrics reported at

periodic meetings like Product Quality Data Review (PQDR / Indicators),
Management Review Board (MRB) and CAPA Review Board (CRB) of both
CAPA and Complaints system.
Provide support such as coaching, instruction, mentoring and / or consultation
for the CAPA-complaints process. Support maintenance of indicators for
decision making purposes in different areas and update of Trackwise 8 (TW8).
Keep in compliance with SOPs, GQPs, GMP, GDP, FDA, ISO requirements,
and other Regulatory Agencies regarding CAPA and Complaints processes.
Standardized, consolidate investigations of different types of process /
products deviations in order to ensure consistency among them, proper
classification of non-conformance, as well as to ensure that proposed actions to
correct them do not contradict actions already implemented.
Perform CAPA complaints trainings at the facility when applicable.
Assure that the receipt, revision, investigation, response and documentation of
the complaint is according to local and corporate requirements.
Perform Risk evaluations as required.
Responsible for receiving and handling complaints samples. Samples should
be locked and handled with the precaution and cares required by local and
Corporate EHS as some of them might be decontaminated.
Responsible for an immediate notification and awareness to Quality
Management of potential Quality situations.
Submit improvements and / or modifications to specifications and Standard
Operating Procedures as required.
Revise and document information related to complaints such as: Batch
Reviews, Sample Evaluation, complaint evaluation, conclusion among others in
the corresponding electronic system.
Perform the evaluations of reported trends and threshold exceeded in the
complaints system.
Handle on a timely manner any project / activity as assigned by management
or direct supervisor.

Quality Engineer
Nombre de la empresaOscor Caribe
Fechas de empleoago. de 2016 actualidad

Duracin del empleo1 ao y 1 mes

UbicacinZona Franca Industrial Las Amricas

Quality Metrics Coordinator:

-Corrective and Preventive Actions (CAPA).
-Nonconformities.
-Process Deviation.
Follow up the open CAPAS and NC.
Proceed to open the CAPAS and NC that are presented in Oscor Caribe.
Participate actively in interdisciplinary teams to solve the problems generated
by Non-Conformities.
Manage Supplier Corrective Action Request (Scars and Investigations.
Provide support during internal and external audits.
 Provide Audit Response and Implementation Action Planning.
Write procedure for GMP/ GDP Improvement.
Expand communication and exchange of information with our sister plant
(Oscor Inc.).
Participate in Cross Training of Validation Process.

Complaint Technician
Nombre de la empresaHospira
Fechas de empleojun. de 2013 dic. de 2015

Duracin del empleo2 aos y 7 meses

UbicacinParque Industrial Itabo, Haina SC

Collect and analyze trend of all data related to the customer complaints.
Conduct investigations of documents related to customer complaints.
Prepare and report all necessary information to the complaints review board.
Analyze customer complaints of the return samples in order to confirm the
failure mode and obtain the root cause of the customer complaints.
Update the procedure of customer complaints as needed.
Perform analysis of Batch Record review and Lot History Review.
Expand communication and exchange of information with corporate entities.
Participate actively in interdisciplinary teams to solve the problems generated
by Customer Complaints.
Participate in corrective and preventive actions (CAPA) and investigations of
nonconformities (NC).
Provide support during internal and external audits.
Prepare reports of metrics of the Complaints department.
Present metrics of the Complaints Department to management in the meetings
of the plant (Quality Review Board and Management Review).

MFG/Warehouse
Nombre de la empresaRockwell Automation
Fechas de empleoabr. de 2009 mar. de 2011

Duracin del empleo2 aos

1. Material Flow Coordinator:
(Encargada del control del despacho e inventario de materiales en WIP, 15
empleados indirectos, en funcin de Material Handlers, frente a la planificacin y
desarrollo de las rutas de distribucin de cada material handlers, velando por el
correcto inventario en wip y a la vez desarrollando proyectos de reduccin de
discrepancias e inventario en WIP, flujo continuo, optimizacin de tiempos de
respuesta de abastecimiento de material en lneas de produccin) Rockwell
Automation. 2010-2011.

2. Tcnico en Lean Manufacturing:

(Encargado del rea de 5S y asistente en rea de proyectos, 3 empleados
indirectos, implementacin de estrategias Lean y six sigma, mantenimiento de las
herramientas de 5S en lneas de produccin, auditorias 5S e ISO) Rockwell
Automation. 2010.

3. Tcnico de Ingeniero de Manufactura:

(Elaboracin e implementacin de instrucciones de manufactura, Implementacin
de herramientas de ingeniera/Lean para el control de los sistemas de procesos y
Anlisis de modo de fallas, Control Plan y PFMEA, determinacin de tiempo y
estudio operacional, diseo de diagramas de flujo de operaciones y Standard
Worksheet, participacin en implementacin de proyecto Kaizen y cambios de
Layout, conduccin de entrenamientos en la implementacin de nuevos procesos,
elaboracin y realizacin de auditorias internas de 5s y EHS, resolucin de
problemas de produccin asociados al flujo y proceso de productos) (Lneas de
Safety) Rockwell Automation. 2008-2010

4. Pasante de Transferencia:
(Elaboracin y control de las instrucciones de manufactura de lneas de produccin
transferidas) Rockwell Automation. 2008

Pasante de Produccion
Nombre de la empresaIndustrias Monegro
Fechas de empleoene. de 2009 mar. de 2009

Duracin del empleo3 meses

UbicacinParque Industrial Hainamosa

Asistente de Ingeniero de Procesos:

(Soporte en rea de documentacin de procesos, diseo de flujograma de las
operaciones, desarrollo e implementacin de planificacin estratgica)
Industrias Monegro. 2008
 Experiencia

Quality Manager
Nombre de la empresaBanco BHD Len
Fechas de empleomar. de 2017 actualidad

Duracin del empleo6 meses

Define, Develop and Manage the implementation of the Data Governance

program.

NC and Quality Metrics Section Manager

Nombre de la empresaHospira
Fechas de empleojul. de 2016 mar. de 2017

Duracin del empleo9 meses

Responsible of: Non Conformances, Quality Metrics and Post-Market

Complaints Areas
- Administrate Nonconformance System and serves as appointed Meeting
Owner for plant Management Review (MR) and Nonconformance Review Board
(NCRB) along with all Complaints and Post-Market Feedbacks.
- Ensure plants established Nonconformance System, Management Review
and Complaints data gathering processes are aligned with the most current
industry practices and are in compliance with
regulatory requirements. The long-term goal is to prevent re-occurrence of
quality systems
failures, and to achieve top levels of regulatory compliance with the
Nonconformance System, Management Review and Complaints Processes.
- Plant Quality Manager delegated as Management Review (MR) Meeting
Owner to ensure Site Management Review and other Quality Operational
Review Meetings are properly coordinated
and metrics are properly compiled.
- Lead monitoring and analysis of existing Quality Data Sources and developing
 standard reporting models with visualizations to aid decision making and overall
strategy.
- Overall administration of plants Nonconformance System and Complaint
System to ensure a Nonconformance and Complaints Handling Process are in
place, per Global Requirements, for identification of quality issues that could
jeopardize product quality and other events that impacts the quality system and
also serves as a chair of site NCRB and CRB.
- Prevent re-occurrence of quality systems failures, and to achieve top levels of
regulatory compliance with the Nonconformance System, Management Review
Process and Complaints Handling program.
- Communicate with peers and staff to evaluate quality events, ensure proper
segregation, documentation, evaluation and disposition in the Nonconformance
system and Complaints Program.
- Serves as a site SME of the Infinity QS system for data collection and track
and trending of nonconformance and other quality metrics.

Validation Section Manager

Nombre de la empresaHospira
Fechas de empleoago. de 2014 jul. de 2016

Duracin del empleo2 aos

- Manager of Validation Engineering department in HDR facility.

- Responsible for conducting validation activities to verify feasibility of a change
and / or improve the process prior to implementation by using engineering and
statistical analysis tools.
- Manage projects process changes aimed at reducing market complaints,
optimize the use of resources, cost reduction, among others.
- Leading research and analysis process when deviations or defects are
detected, ensuring the implementation of containment, corrections, corrective
and preventive actions.
- Support Corporate Projects.
- Act as Validation SME during all regulatory assessments.

 Senior Process Engineering Supervisor

Nombre de la empresaHospira
Fechas de empleoago. de 2011 ago. de 2014

Duracin del empleo3 aos y 1 mes

UbicacinDominican Republic

- Head of Process Engineering department of the facility, responsible for

evaluating the improvements of different manufacturing processes performed in
the plant.
- Responsible for conducting feasibility assessments to verify feasibility of a
change and / or improve the process prior to implementation by using process
analysis tools.
- Manage various projects process changes aimed at reducing market
complaints, optimize the use of resources, cost reduction, among others.
- Leading research and analysis process when deviations or defects are
detected, ensuring the implementation of containment, corrections, corrective
and preventive actions.
- Support Corporate Projects.

Technical Process Quality Supervisor

Nombre de la empresaHospira
Fechas de empleojul. de 2009 ago. de 2011

Duracin del empleo2 aos y 2 meses

UbicacinRepblica Dominicana

Responsible for the areas of: Technical Process Quality, Quality Assurance
and Statistical Software Quality Engineering.
- In charge for ensuring regulatory compliance within validation system. Assures
conformance with regulations of the FDA and other international regulatory
agencies.
- Accountable for ensure the proper verification of the validation processes for
equipment and machinery, technology transfer, design and introduction of new
products by assuring that project management and validation protocols (DQ, IQ,
OQ, PQ, PV) meet specifications, guidelines and policies established by the
Corporate and external entities such as FDA and ISO.
- Assess and document the impact of the introduction of new computer systems
 to our quality system or changes to the existing ones.
- Confirm by using statistical tools that the validated systems are kept in
control.
Leading continuous improvement initiatives through Lean and Kaizen events.
Members of different plant teams (for transfers from other sister plants).
Leader in the implementation of significant projects in plant quality; including
the introduction of use the risk management tools within the Validation System.

Incoming, Supplier and Process Quality Supervisor

Nombre de la empresaHospira
Fechas de empleodic. de 2008 jul. de 2009

Duracin del empleo8 meses

UbicacinRepblica Dominicana

Responsible for the following areas:

- Incoming Quality, ensuring verification of the raw material used in the plant,
ensuring that they meet specifications.
- Supplier Quality, maintaining direct contact with suppliers of the raw materials.
Managing supplier notifications and ensuring that they establish corrective and
preventive action when a non conformance is notified by plant. Negotiate with
suppliers for the proper disposition of nonconforming or suspects materials.
- Process Quality, analyze process metrics such as DPM, manufacturing quality
data, materials and final product variance, defects analysis and investigations,
control sterilization and testing programs. Evaluate test equipment and
instruments. Monitor product data to identify statistically significant trends and
risks.
Implementation of improvements to costs reduction.
Plant representative in Corporate Supplier Quality Board.

Quality Validations Engineer

Nombre de la empresaHospira
Fechas de empleonov. de 2007 dic. de 2008
 Duracin del empleo1 ao y 2 meses
UbicacinRepblica Dominicana

Responsible for the verification of the validation process for equipment,

technology transfer, design and introduction of new products. Assures
conformance with regulations of the FDA and other international regulatory
agencies.
Review and Approve validation packages for software validation, facilities,
utilities, laboratory equipment and processes.
Participate in product transfer equipment, equipment, instruments, processes,
and software testing.
Member of the Calibration Committee, Statistical Team and Quality Verifiers
Team.
Leader in the implementation of improvements using benchmarking tool with
other sister plants.

Manufacturing Engineering Technician

Nombre de la empresaHospira
Fechas de empleooct. de 2006 nov. de 2007

Duracin del empleo1 ao y 2 meses

UbicacinRepblica Dominicana

Responsible of the following processes:

o Validation of equipment and tools
o Technology transfer support
o New product introduction
o Project management and validation package administration (DQ, IQ, OQ, PQ,
PV).

Production Assistant
Nombre de la empresaParmalat SA (Pty) Ltd
Fechas de empleoene. de 2006 oct. de 2006
Duracin del empleo10 meses
UbicacinRepblica Dominicana

Generate reports and conducting statistical analysis in order to evaluate the

KPI (Key Performance Indicators). Prepare management reports.
Support Operations Manager and Senior Production Supervisor on
administrative duties.
Management of all plant documentation.
Support Production supervisors activities including act as Production
Supervisor.
Support the creation of Production module within the internal system
developed by the company.

- 13 years experience in industry and 9 years in the pharmaceutical industry specifically

in medical device industry.
- Experience with ISO, GxP, FDA, Japan or other key regulatory bodies.
- Knowledge of Quality Management Systems and experience on Design Transfer,
Validation, Document Control, Incoming, Process, Supplier and Software Quality.
- Knowledge of engineering tools for analysis and process improvement.
- Focus on teamwork, results-oriented, project management, commitment,
responsibility, leadership, conflict management, negotiation and good human relations.

Quality, Operations and Engineering Professional, ASQ CQE

REQUIREMENTS
These are the requirements, experience and exam specifics for a Certified Quality
Engineer.

Work Experience
Candidates must have eight years of on-the-job experience in one or more of the areas
of the Certified Quality Engineer Body of Knowledge.

A minimum of three years of this experience must be in a decision-making position.

"Decision-making" is defined as the authority to define, execute, or control
projects/processes and to be responsible for the outcome. This may or may not include
management or supervisory positions.

Candidates must have worked in a full-time, paid role. Paid intern, co-op or any other
course work cannot be applied toward the work experience requirement.
 For candidates who were certified by ASQ as a quality auditor, reliability engineer,
supplier quality professional, software quality engineer or quality manager, the
experience used to qualify for certification in these fields applies to certification as a
quality engineer.

Education
Candidates who have completed a degree from a college, university or technical school
with accreditation accepted by ASQ, part of the eight-year experience requirement will
be waived, as follows (only one of these waivers may be claimed):

Diploma from a technical or trade school one year will be waived

Associate degree two years waived
Bachelors degree four years waived
Masters or doctorate five years waived

Degrees/diplomas from educational institutions outside the United States must be

equivalent to degrees from U.S. educational institutions.

Expectations
These are the minimum expectations of a Certified Quality Engineer.

Will have a fundamental understanding of quality philosophies, principles, systems, methods,

tools, standards, organizational and team dynamics, customer expectations and satisfaction,
supplier relations and performance, leadership, training, interpersonal relationships,
improvement systems and professional ethics.
Will have a fundamental understanding of a quality system and its development,
documentation and implementation to domestic and international standards or requirements.
Will have a basic understanding of the audit process including types of audits, planning,
preparation, execution, reporting results and follow-up.
Will be able to develop and implement quality programs, including tracking, analyzing,
reporting and problem solving.
Will be able to plan, control and assure product and process quality in accordance with quality
principles, which include planning processes, material control, acceptance sampling and
measurement systems.
Will have basic knowledge of reliability, maintainability, and risk management, including key
terms and definitions, modeling, systems design, assessment tools and reporting.
Will have a thorough understanding of problem-solving and quality improvement tools and
techniques. This includes knowledge of management and planning tools, quality tools,
preventive and corrective actions, and how to overcome barriers to quality improvements.
Will be able to acquire and analyze data using appropriate standard quantitative methods
across a spectrum of business environments to facilitate process analysis and improvements.
 BODY OF KNOWLEDGE
The topics in this Body of Knowledge include subtext explanations and the cognitive
level at which the questions will be written. This information will provide useful
guidance for both the Exam Development Committee and the candidate preparing to
take the exam.

The subtext is not intended to limit the subject matter or be all-inclusive of that material
that will be covered in the exam. It is meant to clarify the type of content that will be
included on the exam. The descriptor in parentheses at the end of each entry refers to
the maximum cognitive level at which the topic will be tested. A complete description
of cognitive levels is provided at the end of this document.

Download the Certified Quality Engineer Body of Knowledge

DOW NL O AD P DF (55 KB)

PREPARE FOR THE EXAM

ASQ designed these resources to help you get ready to take the exam. Have you already
reviewed these items? Then choose an exam date below.

Review a list of references that provide the basis for the exam questions. These items
give you a better idea of the material covered in the exam.

Take an interactive sample exam to receive additional feedback on the questions that
appear in the sample exam. Print out the paper-and-pencil sample exam (PDF, 259 KB)
to see the actual test format, including instructions and test questions from past exams.

ASQ offers many books and training opportunities to help you prepare.

Training
Certified Quality Engineer Certification Preparation - Classroom or Web-based
Certified Quality Engineer Question Bank: Certification Preparation
Introduction to Quality Engineering
More Related Training

Books
The Certified Quality Engineer Handbook, Fourth Edition
The ASQ CQE Study Guide
Practical Engineering, Process, and Reliability Statistics
Practical Attribute and Variable Measurement Systems Analysis (MSA): A Guide for Conducting
Gage R&R Studies and Test Method Validations
Practical Reliability Engineering, Fifth Edition
 Quality Audits for Improved Performance, Third Edition
The Uncertainty of Measurements: Physical and Chemical Metrology: Impact and Analysis
Concepts for R&R Studies, Second Edition
Reliability Statistics
Failure Mode and Effect Analysis: FMEA From Theory to Execution, Second Edition
ANSI/ASQ Z1.4-2003 (R2013): Sampling Procedures and Tables for Inspection by Attributes
ANSI/ASQ Z1.9-2008 Sampling Procedures and Tables for Inspection by Variables for Percent
Nonconforming
The Quality Toolbox, Second Edition
Juran's Quality Handbook, Sixth Edition
Supplier Management Handbook, Sixth Edition
Search for more ASQ books

Examination
Each certification candidate is required to pass an examination that consists of multiple-
choice questions that measure comprehension of the Body of Knowledge.

Computer Delivered - The CQE examination is a one-part, 175- multiple choice

question, five-and-a-half-hour exam and is offered in English only. 160 multiple choice
questions are scored and 15 are unscored.

Paper and Pencil - The CQE examination is a one-part, 160- multiple choice question,
five-hour exam and is offered in English only.

All examinations are open book with the exception of the constructed response (essay)
portion of the CMQ/OE exam. Each participant must bring his or her own reference
materials. Use of reference materials and calculators is explained in the FAQs.

Senior Executive HR
Nombre de la empresaFord Motor Company
Fechas de empleomar. de 2014 actualidad

Duracin del empleo3 aos y 6 meses

Handling all HR Policies, Procedures and Functions including Talent

Management & Acquisition, recruitment, onboarding, employee records,
database management, attendance and leave management.
Discipline and grievances
KRA and PMS
Statutory Compliances
Employees Relations
HRMIS
 HR Audit
Exit Management

Edesur Dominicana, Torre Serrano, Av. Tiradentes #47, Ensanche Naco, Distrito Nacional
10124, Repblica Dominicana

Encargado Inteligencia de Perdidas

Nombre de la empresaEdesur Dominicana, S.A

Disear las estrategias de estudio y anlisis del consumo y la informacin comercial de

los clientes para reducir el ndice de prdidas a travs de la deteccin de
irregularidades y la propuesta de mejoras a la gestin existente en los clientes no tele
medidos.

11
Contraer la seccin de cursos

cursos
Nombre del cursoAdvanced Quality Planning (AQP) Workshop
Nombre del cursoDesign Control Training
Nombre del cursoDesign of Experiments Training
Nombre del cursoDiplomado "Mejoramiento Continuo": Modulo SPC (Control
Estadstico de Proceso)
Nombre del cursoGood Technical Writing Training
Nombre del cursoGreen Belt Training
Nombre del cursoMedical Devices: Quality Management Systems: International
Standard ISO 13485:2003 and 21 CFR Part 820
Nombre del cursoMinitab and Basic Statistics Training
Nombre del cursoPQ and PPQ Training
Nombre del cursoSelf Track Training: The Oz Principle
Nombre del cursoTest Method Validation Training
 1
Contraer la seccin de certificaciones

certificacin
TtuloPMP
Fecha de la certificacinmar. de 2016 mar. de 2019 Licencia 1913787

Autoridad emisora de la certificacinProject Management Institute

INFOTEP
Nombre de la titulacinEvaluacin de Proyectos
Fechas de estudios o fecha de graduacin prevista2016 2016

Anlisis econmico de los proyectos

INFOTEP
Nombre de la titulacinTcnicas de Negociacin
Fechas de estudios o fecha de graduacin prevista2016 2016

Universidad Iberoamericana
Nombre de la titulacinPreparacin para Certificacin en Project
Management Professional
Fechas de estudios o fecha de graduacin prevista2015 2015

INFOTEP
Nombre de la titulacinFacilitador de la Formacin Profesional
Disciplina acadmicaEducacin
Fechas de estudios o fecha de graduacin prevista2014 2014
Escuela de Organizacin Industrial
Nombre de la titulacinMaster Business Administration
Disciplina acadmicaMaster Ejecutivo en Administracin de Empresa
Fechas de estudios o fecha de graduacin prevista2009 2010

Mster Especializado para el desarrollo de habilidades directivas,

especializacin en Planificacin, Estrategias, Finanzas, Marketing, Recursos
Humanos y Cadena de Abastecimientos.

Docente
Nombre de la empresaInstituto Especializado de Estudios Superiores
Loyola (IEESL)
Fechas de empleomay. de 2009 actualidad

Duracin del empleo8 aos y 4 meses

UbicacinRepblica Dominicana

- Docente de Introduccin a la Ingeniera

Project Engineer III

Nombre de la empresaFenwal, Inc., a Fresenius Kabi Company
Fechas de empleomar. de 2010 actualidad

Duracin del empleo7 aos y 6 meses

UbicacinRepblica Dominicana

Ingeniera de Proyecto
- Evaluacin Financiera de Proyectos
- Business Case
- Preparacin de documentacin de inicio, estimacin, planificacin y
presupuesto.
- Identificar riesgos y elaborar planes de respuesta.
- Liderar el equipo de proyecto, incluyendo gestin de los dems
departamentos de soporte.
- Seguimiento de las actividades.
- Alertar y tomar acciones correctivas y preventivas sobre desviaciones.
- Organizar y facilitar las reuniones de seguimiento.
- Modificacin de planes para incluir cambios de alcance acordados.
- Validacin de procesos, maquinarias y equipos
- Mejora de Proceso

Facilitador
Nombre de la empresaINFOTEP
Fechas de empleooct. de 2015 actualidad

Duracin del empleo1 ao y 11 meses

Facilitador autorizado de las acciones formativas: Gestin de Proyectos,

Procesos y Procedimientos.

Cesarina Ramirez, MBA, PMPOcupacin del miembroProject

Management / Continuous Improvement

English Language Instructor

Nombre de la empresaEnglish Learning Center
Fechas de empleooct. de 2015 may. de 2016

Duracin del empleo8 meses

UbicacinSan Cristobal, San Cristobal

To facilitate the learning of the English language at different levels and ages
(children, young people and adults) so that they are able to communicate with
people from English speaking villages.

Mateo 21 : 21-22 Les aseguro que si ustedes tienen fe y no dudan - les respondio
Jesus- 22 SI USTEDES CREEN,RECIBIRN TODO LO QUE PIDAN EN ORACIN

Supply Chain Professional with more than 12 years of experience in Operations

management, Inventory Planning, Strategic Purchasing and implementing improving
systems like Sales and Operations Planning in Multinational companies importing
materials and finished goods from diverse suppliers in the world. I strive for continued
excellence and have achieved several International Certificates in Logistics
Management and Planning. Very fluent skills speaking and writing in English and
Spanish and vast experience in Administrative functions as well.