LUIS A. CABELLO TORRES, P.E.

*** ******* *****

Auburn, Alabama 36830

(787) 636- 4382 (Mobile)

334-***-****(Work)

E-mail address: acoku8@r.postjobfree.com

OBJECTIVE

A challenging position on the Managerial, Process Excellence or

Quality field in an innovative company in which I could develop

an excellent professional career with the abilities, skills and

knowledge acquired during more than 20 years of working

experiences and educational background.

LICENSE / CERTIFICATIONS

Professional Engineer License # 12427 (Puerto Rico)

Certified Six Sigma Black Belt - AIT / The Tech Group

Certified ISO 13485 Lead Auditor - Stat-A-Matrix

EDUCATION

University of Puerto Rico, Mayaguez Campus

Bachelor of Science on Industrial Engineering - May 1991

Turabo University, Caguas Campus

Master Degree on Business Administration (Management)

December 1999

Advanced Integrated Technologies, Inc.

Phoenix, Arizona

Six Sigma / Black Belt Training Sept 2001 - March 2002

EXPERIENCE

05/2013 - present

SiO2 Medical Products - Auburn, Alabama

Sr. Supplier Quality Engineer

. Design and implement the Supplier Quality Program including

the development of the necessary procedures, work instruction

and forms.

. Review and provide input for supplier selection activities,

including supplier evaluation and quality systems audits.

. Assess supplier process capability for new components,

processes, assemblies and/or purchased finished goods.

. Monitor supplier performance and coordinate continuous

improvement activities with suppliers.

. Assist suppliers with conducting FMEA, process capability

studies and DOE.

Monitor supplier performance and maintain supplier

scorecards.

. Assist in developing and implementing methods and procedures

for inspecting, testing and evaluating the precision,

reliability and accuracy of supplier products and processes.

. Coordinate with customers and suppliers relating to quality

performance, trends and corrective actions.

. Verify compliance and effectiveness of the quality system by

performing supplier audits and surveys.

. Work with suppliers to continuously improve products and

processes through lean manufacturing and six-sigma principles

and techniques to assure the quality of goods and services

provided.

. Ensure that non-conforming material from suppliers is

disposition in a timely manner and analyze defect trends, in

order to initiate appropriate corrective action.

Page 2 of 3 (LCT Resume)

05/2012 - 05/2013

Novartis Ex-Lax - Humacao, P.R.

Supplier Quality Engineer

Responsible as Supplier Quality Engineer of the following:

. Implementing the Supplier Quality Program for Novartis Ex-Lax

. Maintain and improve quality standards of supplied

components, raw materials and ingredients.

. Lead assessment and qualification approval processes for

suppliers.

. Develop inspection criteria for raw materials and packaging

components.

. Direct supervision of the Incoming Area and personnel.

. Responsible for TPO (Third Party Operations) quality

standards maintenance and improvements.

07/2009 - 05/2012

The Tech Group - West Company - Cidra, P.R.

Manufacturing Engineer

Responsible as Manufacturing Engineer of the following:

. Project Management responsibility to complete the transfer,

validation and approval of new or transfer molds.

. Develop, execute and complete IQ's, OQ's and PQ's for new

equipments, machines and molds.

. In charge of the direct communication and projects for

different key customers like Pall, Medtronic, Cooper Vision,

Aspen and Fenwal.

. Member of the Internal Audits and Six sigma Lean

Manufacturing Team.

04/2005 to 07/2009

Bard Shannon Puerto Rico - Humacao, P.R.

Supplier Quality Engineer II/ Incoming Supervisor

Responsible as a QA Engineer of the following:

. Responsible for the Suppliers Quality Program.

. Member of the facility CAPA Team and EHS Department

Representative.

. Responsible for all the Supplier On-site Audits and Self

Assessment schedule completion.

. Responsible for the Incoming Inspection Department and the

Warehouse QC HOLD Cage management.

. Support all the machine and products transfer and validation

projects for the Plant relocation using Project management

skills including teamwork, Six Sigma, Lean, New Supplier

audits, etc..

. Member of the FDA CAPA Team to complete the response, actions

and implementation for the FDA 483 audit observations.

04/2000 to 11/2004

The Tech Group, Inc. - Cidra, P.R.

Quality Assurance Manager

Responsible as a QA Manager of the following:

. Direct responsibility of the Quality Operations and Quality

Engineering functions.

. Direct Responsible for the Applied Statistic SPC Software

implementation for all the manufacturing lines at molding and

assembly areas.

. In charge of the Green Belt and White Belt Candidates

Training and Development to assure the implementation of the

Process Excellence program at TGPR.

. On Charge of the Documentation System and ISO 9001-2000

compliance.

. Responsible of the Internal Audits System and Calibration

program.

Page 3 of 3 (LCT Resume)

04/1997-04/2000

Nypro Puerto Rico, Inc. Cayey, P.R.

Quality Operations Manager

Responsible as a Quality Operations Manager of the Following:

. On charge of the quality operations functions for the Cayey

II (Pharmaceutical) and Cayey III (Non-Sterile) Molding

Plants.

. Responsible for the improvements of In-Process and Final

Inspections area and direct supervision of the Internal

Calibration Program.

. Support all the machine and products transfer and

validations.

. Responsible of the Direct Communication with our clients to

assure the Customer Satisfaction all the time.

03/1995-04/1997

Becton - Dickinson - Micropette, Inc. San Lorenzo, P.R.

Process Engineer

Responsible as Process Engineer and Supervisor of the

following:

NGMBT Printing Improvement Project completion.

Achieve over $75,000 in labor and waste cost reduction.

Responsible for the Engineering Department Budget monitoring.

Responsible for the new process and machine validations and qualifications.

Lead Engineer for all the NGMBT new Improvement process including all

validations completion since the start-up.

. Responsible for the MBT area Production Schedules Completion.

01/1992-11/1993

Baxter Healthcare Corporation, Edwards Division, A asco P. R.

Q. A. Engineer & Supervisor

Responsible as a Q.A. Engineer of the following:

New sampling methods development and implementation.

SPC Program support and implementation.

Achieve over $100,000 on sampling cost reduction.

Product Transfer and Process Validation responsible for the LIS family

products.

Responsible as a Q.A. Supervisor of the following:

Direct supervision of twenty (20) inspectors and two (2) group leaders.

Responsible for the Product Verification and Quarantine areas.

SKILLS

. Bilingual - English / Spanish

. Six Sigma and Lean manufacturing Knowledge

. Good Team worker and problem solving.

. Self starter and good communication skills

. PC Software knowledge

. Knowledge of GMP's, GDP's and OSHA Regulations

ACTIVITIES / HONORS

P.D.A. member

A.S.Q. member

REFERENCES

Available upon request.

Contact this candidate