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Resume: Quality / Validation Engineering Contractor / Subcontractor

Author: Cezar Lucki

Date: 2000/10/10

Forum: alt.jobs

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Please view my site for more information -> http://qeval.homestead.com

Providing work as any of the following:

* ISO / OSHA / GMP / QSR / QS / DEA / FDA (facility / documentation /

validation) - AUDITOR

* Industrial Hygienist

* Design Control Specialist (FMEA, FTA, hazard analysis)

* MRP / ERP developer

* Statistician

* Quality / Validation Engineer

* Quality Assurance Specialist

* Technical Writer

* Regulatory Specialist Specialist

* CE Marking Specialist

* Metrologist

Working for these industries:

* Pharmaceutical

* Medical Devices

* IVD's

* Biotech

* Diagnostics

* Food

* Aeronautic

* Automotive

* Electronics

* Information Technology

* Manufacturing

Just some of the things I can do for your company:

1. Reduction in Quality Costs.

2. Enhancement in Quality Practices.

3. Enhancement in Research Techniques.

4. Reduction in wasted labor and material.

5. Satisfaction of Federal and Local Government compliance in

your company.

6. Introduction of new technologies, techniques and innovations.

7. Increase in speed, safety and efficiency.

In the end what all this means to you:

1. Increased inter and intra-departmental performance.

2. Increased Profit.

3. Increased Customer Satisfaction.

4. Reduced wasted capital, time and effort.

Cezar is not intimidated by projects outside his area of expertise. He

is motivated, energetic, and resourceful. Cezar will excel in any

environment. I am greatful that he is on my team.

Grace Kwan, Director of Quality & Regulatory Affairs at QDI

There were times when work was chaotic and overwhelming, but his

perseverance and cunning had always prevailed... He

seems to be always sharp and in the lead. He is ambitious and there seems

to be no obstacle that he cannot overcome...

Dr. Robert Gordon PFP,VMD, http://www.monetarystress.com

Cezar is a self starter and always insured that his projects were

completed on time. His communication skills are excellent and he also

helped with departmental training. In addition to his professional

activities, Cezar is very active in many community causes, which he donates

his time working with kids. Cezar's dedication to his job, motivation and

job knowledge makes him a wonderful candidate for future career challenges.

Nannette Monreal MSQA, V.P. of Quality Assurance, Leiner Health Products

Resume Page -> http://qeval.homestead.com/resume.html

Skills Page -> http://qeval.homestead.com/skills.html

References Page -> http://qeval.homestead.com/references.html

Validations Completed -> http://qeval.homestead.com/MyValidations.html

Letters of Recommendation -> http://qeval.homestead.com/testimonial.html

My approach to projects -> http://qeval.homestead.com/testimonial.html

Type of Services provided -> http://qeval.homestead.com/service.html

My rates and conditions -> http://qeval.homestead.com/salary.html

ESUME

Cezar Lucki

abpyay@r.postjobfree.com

http://qeval.homestead.com

OBJECTIVE: To provide professional consulting services.

Competencies: cGMP/GLP/OSHA/QSRValidations Material Control / Inspections /

Purchasing

Internal / Vendor Audits Metrology / Maint. Product Failure analysis /

R&D

IT Management Personnel Training Environmental / Micro. / Chem.

techniques

Pharmaceuticals Solids / Semisolids Medical Devices (I,II, III) / IVDs

NRC / Nuclear Env Ctrl PLC / Sftwr. Val. FMEA / FTA / Design Controls

EXPERIENCE:

MBI / UroCor through Perigon / PTS, Oklahoma City, OK6/00 - 7/00Quality Assurance / Validation Specialist

-

Consulting

MBI / UroCor is a medical device manufacturer of

nuclear sources implants. Supported all Quality Assurance and Validation

functions. Wrote, SOP's for quality assurance, maintenance, calibration,

and use of equipment. Management: Stanley Mills PhD, Jacqueline Mills,

Tarance Grisso, David Caravaglio.

OSHA / IH facility audits and corrective action implement. SOP generation

and revision (20+)

Internal GMP, Documentation and Facility Audits Design Control Development

Project planning for quality issues, PLC and Software Vals. FMEA / FTA /

Hazard Analysis

Managed, created, executed and summarized Equipment and Process

Validations Trained personnel in QSR, GMP, OSHA, design ctrls, latest FDA

req.'s

Oread Pharmaceuticals through QST / Oxford, Palo Alto,

CA2/00 - 6/00Quality Assurance / Validation Specialist

-

Consulting

Oread is a contract pharmaceutical manufacturer of

parenterals, liquid, semi-solid, and solid dose drugs. Supported any

Quality Assurance and Validation functions for contract manufacturer.

Supported technology transfer. Projects were performed for clients such

as: ICN, Roche, Agouron, Praecis, BioMedicines, Guilford, Nissan, Dura,

Unimed and Xoma. Management: Beth Rice, Marji Prows, Tony Brown, Ken Miles

PhD, Arlene Blakes.

Equipment and Process Validations SOP generation and revision

Cleaning Validations Batch Verification

Stability Trending Audit Responses

Internal GMP, Documentation and Facility Audits Investigations /

Troubleshooting

Qualisys Diagnostics, Inc. Irvine / Carlsbad, CA11/98 - 1/00Quality Engineer / Product Support Lead

/ IT Support

Qualisys / Qualigen is an IVD manufacturer for

immunoassay kits by means of electronic assaying devices. Validated lab and

manufacturing equipment, test methods, facility, and mnfg processes.

Oversaw V&V and design transfer. Technical training and assistance.

Supplier and vendor audits. CPA, MRB, Quarantine and Approval process.

Purchasing (over $750K), receiving, and inspections. Control of material

via MRP system. Database development. Industrial hygiene, safety and GLP

establishment. Metrology and basic maintenance. Implemented QSR's and

ISO9000's to all phases. Heavy technical and computer support and

development. Supervisor: Grace Kwan, Glenn Walker, Gary Alvey.

IQ,OQ,PQ execution and protocol generation / V&V SOP generation and

revision

DOE & statistics in clinicals, validation and manufacturing Internal &

Supplier Audits

PMA & 510K assistance / stability management Metrology & Maintenance

Personnel training (QSR's, GLP's, cGMP's, computer) Material Management /

MRP control

Allergan (R&D dept.) (through Kimtec)

Validations Specialist Contractor

Allergan - equipment val. / SOP's / validation records audit

9/98 - 10/98

B. Braun McGaw, Validations / QE Dept., Irvine 4/97 - 8/98Quality Engineer Associate II

B.Braun McGaw is a manufacturer of paranteral

pharmaceuticals and medical devices. Validated/requalified systems, new or

revised products, systems, PLC's, and facilities. Investigated product

complaints. Technical training and assistance. Performed plant shutdown

operations. Supervisor: Nannette Monreal & John Smith / previously Blair

Smith

IQ,OQ,PQ execution and protocol generation SOP generation and revision

Chairing of product eval. and plant coordination meetings DOE, R&R,

Stats. and Mil. Std's

Personnel training (validations, requal, computer, app., etc.) Facility

Audit

Allergan

(QC dept.) (through Lab Support), Irvine

12/96

- 4/97

Environmental Monitoring Microbiology Laboratory /

Chemistry Technician

Allergan is a munufacturer of pharmaceuticals,

medical devices, and cosmetics. Performed environmental monitoring and

chemical analysis. Endotoxin testing of medical devices. 209E forms and

trending. Supervisor: Rod Patterson

Viable testing of water, air, and surfaces. LAL (clot) testing on devices

Gas Chromatography / IR Spectorscopy Non-viable testing of air.

McGaw

(QC dept.) (through Lab Support), Irvine3/96 - 11/96 (f/t) & 11/96 -

4/97

(p/t)

Environmental Monitoring Technician / Media and

Sterility Technician

McGaw is a manufacturer of paranteral

pharmaceuticals and medical devices. Performed environmental monitoring.

Assisted in sterility testing of final product. Led investigations and

performed trending. Supervisors: Myron Civils & Wendy Ricapito

Viable testing of water, air, and surfaces.Non-viable testing of air

SKILLS: COMPUTER

Applications/O.S.: DOS, SigmaStat, SigmaPlot, some UNIX, Access,

Windows2000/95/3.X/NT, Excel, Word, BASIC, Power Point, Lotus Notes &

Organizer, LIMS, Statgraphics, Mathematica 2.2, Harvard Graphics, Project,

TurboCAD 6.0, CorelDraw, network (Novell)

LANGUAGES Basics: Spanish and French

EDUCATION: B.S

. Biological Sciences, specializing in

microbiology, emphasis in chemistry and psychology

.

University of California

at Irvine.

PERFORMANCE HIGHLIGHTS

Tasks at Qualisys Diagnostics, Inc

.

Class II level medical device diagnostics manufacturing facility

1. Quality and Validations Engineering

1.1. Design of Experiment

1.1.1. Conducting own experiments

1.1.2. Taguchi methodology

1.1.3. Process capability, normality analysis, and sample analysis.

1.2. Product design improvements planning

1.3. Product and raw material prospective evaluation.

1.4. Statistical Process Capability (SPC) charting.

1.5. Statistical Quality Control (SQC) implementation.

1.6. FMEA, FTA, HA (Failure Modes and Effects Analysis, Fault Tree

Analysis, Hazard Analysis)

1.7. Feasibility and Stability runs.

1.8. Validations

1.8.1. IQ/OQ/PQ

1.8.1.1. Lab Equipment and production equipment

1.8.1.2. Test Method validations

1.8.1.3. Cleaning

1.8.1.4. Process Validations

1.8.1.5. Validations & Verifications - assisted outside

contractors with software validations.

2. Training

2.1. Training personnel in QSR, cGMP's, GLP, OSHA and ISO9000's

2.2. Computer applications training.

3. Information and Technical Systems

3.1. Customized databases for collecting and controlling information from

instrumentation, metrology, maintenance, documentation, purchased chemical

control, indentured lists, and other controlled systems.

3.2

. All aspects in rolling in new systems and peripherals.3.3

. All technical support - (hardware and software)

3.4. Programming (Excel, Access, and VBA related

)

3.5

. Troubleshooting

3.6

. Training and assistance

3.6.1

. Word, Excel, Access, Win95/98/NT, Project, Luminometer software,

etc.

3.6.2

. Rosys Anthos Robotics (AutoLucy)

4. Production and Process Engineering

4.1. Making suggestions for improvement of process.

4.2

. Implementing facility design into projected product production area

4.3. Challenging designed process plans.

4.4

. Feasibility runs.

5. Documentation

5.1. Revision of existing SOP's and generation of new.

6. Incoming Material Inspection

6.1. Development of database tracking system.

6.2. Development and implementation of labeling system.

6.3. Development of QC sampling and testing, stability retention,

approval, quarantine, MRB assignment.

7. Purchasing

7.1. Responsible for tracking and purchasing lab supplies, information,

and equipment

7.1.1. Responsible for over $750,000 purchased in capital.

7.1.2. Budgeting purchases

7.1.3. Correspondence with suppliers

7.1.3.1. VWR, Scientific Products, Fisher, OHAUS, Omega, etc.

8. Inventory Control

9. Quality Assurance

9.1. Certification of new suppliers/vendors.

9.2. Purchased Chemical Control

9.3. Supporting two 510(k) processes and a PMA.

9.4. CE mark and MDD (Medical Device Directive) support.

9.4. Industrial Hygiene and Safety:

9.4.1. Have created and implementing the following:

9.4.1.1. Biohazard program with blood-borne pathogens

9.4.1.2. Waste management program, identification and

documentation

9.4.1.3. GLP's and all associated safety mechanisms

9.4.1.4. Fire safety program and documentation

9.4.1.5. Emergency evacuation program

9.4.1.6. EPA (Hazardous Waste and OSHA regulations).

10. Metrology

10.1. Corresponding with local contracting agencies in

the implementation of calibration system.

10.2. Assuring NIST traceability is maintained with all

applicable instrumentation

10.3. Exploring cost vs. in house calibration

alternatives

10.3.1. Implementing Handbook 44 and 130 in calibration procedures.

10.4. Accounting all equipment is traced and applicable

calibration schedule is maintained.

10.5. Performed Calibration and R&R.

10.5.1. Pipettes

10.5.2. Balances

10.5.3. Mixers

10.5.4. Thermometers

10.5.5. Graduated Cylinders

11. Maintenance (preventive and emergency)

11.1. Creating and implementing of maintenance program

for lab equipment and production equipment as they are being acquired.

Quality / Validation Engineering - B Braun McGaw

Product complaints investigation - Product Service/Incidence Report

(PSR/PIR)

Decontamination processing of returned product (hazardous materials

approach)

Physical evaluation

Coordination of product testing with laboratories (e.g. chemistry,

microbiological, BTC, engineering, etc.)

Summarization of laboratory results in technical reports

Issuance of corrective action if applicable

Identifying areas of common product issues

Presenting suggestions for product improvement and trend analysis

Validations (Installation, Operational, and Performance Qualification)

PLC, systems (retrospective), facilities, equipment and product

Protocol generation and execution

Coordination of validations with applicable departments

Validation summarization

Product Test Run Authorization execution and creation of testing method

Some - Design of Experiment generation, coordination and execution

Statistical evaluation with respect to Cpk, confidence level, military

standards, etc.

Final deposition of product based upon the statistical evaluation and

product performance

Quality Control Release Verification (QCRV) coordination

Review of Maintenance Orders and assignment of Change Control

Validation or QCRV

Coordination of sampling plans and required testing with laboratories

Release of classified and controlled facilities,

distilled/deionized/softened water, compressed air, pumps, steam,

sterilizers, etc. upon receipt of applicable data in compliance with company

and government regulations

Addressing problem facilities/systems/products and identifying trends

Tracking the maintenance progress and laboratory results

Meeting presentations - As Acting Chairperson

Product investigation updates and statistical evaluation

Validation updates and coordination

QCRV / Change Control Request coordination meetings with maintenance

department and laboratories

SOP generation/revision and Document Orders

Revision of Standard Operating Procedures, Technical Information

Standards, etc.

Creation of quantitative sampling plan with aid of mil. standards or

other statistical approach

Knowledge of Plastics and LVP fabrication / filling

EXCEL, DUPLEXT, PAB, Glass, PICT, Add-A-Vial, addEASE,

Compounding, SafeLine, Injection Molding, Blow Molding, Film Extrusion

Technical Training of Personnel

Computer training - Windows/NT, Excel, Word, Network (Novell), Lotus

Organizer & Notes

New Test Methods, Validation, QC Release Verification

Technical Assistance

Computer, applications, network, printer and other assistance

Requalification / Validation approach and procedures

Internal Audits

Routine and unscheduled facilities and process audits

High Involvement Team member

Involved with teams, in efforts of modernizing and improving specific

aspects of the company

Laboratory

Chemistry

Infra Red Spectrum analysis - Perkins Elmer

Liquid and Solid

Gas Chromotography - Hewlette Packard 6890 II

Standards and Sample testing

Obtaining results within a minimum of 99% correlation of obtained

Linear Regression

Maintenance of machine, peripherals, computer, printer, gas delivery,

headspace, gas tanks

Troubleshooting

Ultra -violet Spectrum

Spectrophotometer

pH analysis

Electronic

Titration method

Atomic Absorption analysis

Biological

Biochemical

Electrophoresis

Western Blotting

Immunoblotting

Microbial

Limulase Amebocyte Lysate (clot) testing of surgical devices

Auxonographic testing of Antibiotic affectivity

Bioburden testing of air water, plastics, surgical devices, and

solutions

Filtration and incubated growth on TSA plate

Heat Shock

Inoculating

General biochemical ID techniques

Gram Staining, acid-fast stain, OF-Glucose, Oxidase, Catalase, etc.

Microbial Enumeration

Surface testing

RODAC

Swab

Sterilizer use - Castle / Amsco

Environmental Monitoring

Particulate Matter monitoring in water and air using HIAC or MetOne

Velocity of air using AIRVELO

Pressure, temperature, and humidity monitoring

HEPA hood leak testing

Data trending

LIMS

Completed Validations and Sub-Validations

1. QCRV - Quality Control Release Verification

1.1. WFI -water for irrigation lines

1.2

. Power Plant

1.2.1

. Holding Tank

1.2.2. Sterilizers

1.2.3. Still

1.2.4

. Compressed Air

1.2.5

. Steam and Condensate return lines

1.2.6

. Co-gens

1.3. Clean Room repairs and upgrades

2. PTRA - Production Test Run Authorization

2.1. Conveyor PLC change and proximity switch installation

2.2. New Inkjet Printer Installation

2.3. Boxing equipment change and installation

3. Process

3.1

. Compounding

3.1.1

. Antibody

3.1.2. Microparticle

3.1.3

. Wash buffer

3.2

. Filling Precision and Accuracy

3.3. Pouch Fabrication

3.4

. Bag Fabrication

3.5

. Bottle injection molding design specifications

4. Equipment

4.1. Manufacturing

4.1.1

. Bag washers and rinsers

4.1.2

. Washing machines

4.1.3. Fillers

4.1.4

. Component Washers and Driers

4.1.5

. Injection molding machines

4.1.6

. Film extrude

4.1.7

. Blow Molders

4.1.8

. Labeling and printing machines

4.1.9

. Boxing and ink dispensers

4.1.10

. Conveyors and associated mechanisms

4.1.11

. Ultrasonic welders

4.1.12

. Component assembly machines

4.1.13

. Hoods

4.1.14

. Stills

4.1.15

. Filters (including integrity tests)

4.1.16

. Homogenizer

4.1.17

. Steam, compressed air and WFI lines

4.1.18

. Facility

4.2. Lab

4.2.1

. FPLC

4.2.1.1

. Against standards

4.2.2. Refrigerators

4.2.3. Freezers

4.2.4. Incubators

4.2.5. Spectrophotometers

4.2.6

. Purified and Deionized water

4.2.7

. Bag parallel and cylindrical burst pressure testers

4.2.8

. Plunger activation machine

5. Cleaning

5.1. Compounding Equipment

5.2. Facility Sanitation

6. Sterilization

6.1. Sterilization Tank Validation assistance

6.1.1. Viable and non viable testing

6.1.2. Pressure and Filter Integrity

6.1.3. Fo Limits - Steam, EtO

6.1.4. BI testing

7. PLC

7.1. Capping machine PLC change

7.2. Bag fabrication Machine

7.2.1

. Alarms challenge

7.2.2

. Parameter challenge

7.2.3

. Proximity switches

7.2.4

. Temperature sensors

7.2.5

. Environmental Controls

7.2.6. Robotics

8. V&V (software and hardware)

8.1. FastPack Analyzer

8.1.1. FTA (fault tree analysis)

8.1.2

. FMEA (failure mode and Error analysis)

8.1.3

. Software Validation assistance

8.2. Equipment and Documentation Control System - Access dBase

8.2.1

. FTA (fault tree analysis)

8.2.2

. FMEA (failure mode and Error analysis)

9. Test Method Validation

9.1. QC methods

9.1.1. Physical

9.1.1.1

. Use of calipers in inspections

9.1.1.2

. Use of multimeter in inspections

9.1.2. Chemical

9.1.2.1

. Chemiluminescent assay accuracy and precision, using R&R.

9.1.2.2

. Streptavidin binding assay.9.1.2.3

. Chemiluminescent substrate accuracy and precision.

10. Facility Audits and Validations

10.1. Power plant

10.1.1

. Boiler room

10.1.2. WFI

10.1.3

. Compressed air

10.1.4. Steam

10.1.5

. Condensate Return

10.1.6

. Co-gens

10.1.7

. Chillers

10.2. HVAC and Air Systems

10.3. Clean Rooms (class 100K to 1K)

10.3.1

. Main manufacturing facilities

10.3.2

. Gowning Rooms

10.3.3. Airlocks

10.3.4

. Transfer Rooms

10.3.4.1

. HEPA filtration and integrity

10.3.4.2

. Room air change

10.3.4.3

. Viable and non-viable air

10.3.4.4

. Viable surface

10.3.4.5

. Smoke studies

10.3.4.6

. Positive Pressure

10.3.4.7

. Personnel PM and viable tests.

Continuing Education

Accredited Institutions

University of California

at Irvine - Bachelor's of Science, Biological

Sciences

Non-credited Training

Hazardous Waste Management Training - Allergan, 2/12/97

OSHA Lab Standard Training Course - Allergan, 2/19/97

OCRA (Orange County Regulatory Affairs) FDA IVD Workshop - Irvine CA, 2/2/99

MD&M seminar - BSI registrar and the ISO9000's - Anaheim CA, 2/10/97

cGMP's - McGaw, Inc. (quarterly 1996, 1997 and 1998)

Accredited Adjuncts

MD&M (Medical Design & Manufacturing) workshops - Anaheim CA, 2/7/99

(0.4

units)

Contents:

1. Software Verification and Validation of Embedded Systems

2. Design Transfer

3. Process Validation Guidance

4. Defining a Process During the Operational Qualification

5. Making Process Validation Continuous with Process Monitoring

6. Steps to Implement Design Controls

7. Design Controls for Product Development

MIS154B CMGT574 ( CIS Business Communications)

- University of Phoenix (3

credits)

-

ADDITIONAL SKILLS

Skill Name, Skill Level, Last Used, Experience

510k, PMA - Intermediate - Currently used1 years

Access - Expert - Currently used - 4 years

Atomic Absorption Spec. - Intermediate - +4 years ago -

2 years

Autolucy / Tecan Anthos Rosys - Beginner - Currently used1

years

Castle / Amsco Sterilizers - Expert - 1 year ago - 3

years

CE Marking, MDD, IVDD - Beginner - Currently used - 1

years

cGMP GLP OSHA QSR ISO9000, 9001 reg's - Expert - Currently

used - 4 years

Cleaning Validations - Expert - Currently used - 3

years

Comparitor - Intermediate - 2 years ago - 2 years

Corel Draw 7 - Intermediate - Currently used - 1 years

Design Controls, FMEA, FTA, Hazards - ExpertCurrently used -

1 years

DOE - Intermediate - Currently used - 1 years

DOS - Expert - Currently used - 9 years

Enzyme Immunoassay Analysis - Beginner - Currently used -

1 years

Equipment Validation - Expert - Currently used - 3

years

Ethernet LAN - Intermediate - Currently used - 2 years

Excel - Expert - Currently used - 7 years

Facility Validations - Expert - Currently used - 3

years

FPLC (Pharmacia) - Beginner - Currently used - 1 years

Fractionating (Pharmacia) - Beginner - Currently used - 1 years

Fractionator (Pharmacia) - Expert - Currently used - 1 years

French - Intermediate - 3 years ago - 4 years

Gas Chromotography HP6890 II - Expert - 1 year ago - 1 years

HIAC / MetOne PM counters - Expert - 1 year ago - 3 years

HPLC - Waters - Beginner - 1 year ago - 1 years

IBM PC - Expert - Currently used - 13 years

IMx Spectrophotometer - Beginner - Currently used1 years

Instron (fatigue &tension)Beginner2 years ago3 years

Internal / Vendor AuditsExpertCurrently used3 years

IR spectra - Perkins ElmerExpert1 year ago1 years

IT Training and SupportIntermediateCurrently used2 years

LAL (Endotoxin)Intermediate1 year ago2 years

LIMSExpert2 years ago2 years

Lotus Organizer / NotesExpert1 year ago2 years

Material Control / Inspection / InventoryExpertCurrently used2 years

Mathematica 2.2Intermediate3 years ago2 years

Metrology and Basic MaintenanceIntermediateCurrently used1 years

MicrocalipersExpertCurrently used4 years

MS Frontpage 2000ExpertCurrently used1 years

MS OutlookExpertCurrently used2 years

MS ProjectIntermediateCurrently used1 years

Novell NetworksBeginner1 year ago2 years

NRC regulationsIntermediateCurrently used1 years

Oscilloscopes (various)Beginner+4 years ago2 years

Personnel trainingExpertCurrently used3 years

pH / Conductivity Meters (Accumet)ExpertCurrently used4 years

PLC ValidationsIntermediateCurrently used3 years

Polish (& other Slavic/Cyrillic)IntermediateCurrently used25 years

Power PointExpertCurrently used3 years

Process ValidationIntermediateCurrently used3 years

PurchasingIntermediateCurrently used1 years

R&RExpertCurrently used2 years

SigmaStat / SigmaPlotExpertCurrently used1 years

SoftQuad Hotmetal Web Hosting & DesignIntermediateCurrently used1 years

Software ValidationsBeginnerCurrently used1 years

SpanishIntermediateCurrently used5 years

StatgraphicsExpert1 year ago2 years

Sterilization ValidationIntermediate2 years ago2 years

Stratus and Proteus (ERP system)Intermediate2 years ago2 years

StroboscopeExpertCurrently used3 years

TensiometersExpertCurrently used4 years

Test Method ValidationIntermediateCurrently used1 years

TurboCADIntermediateCurrently used1 years

Typing and 10 KeyExpertCurrently used10 years

UNIXIntermediate1 year ago2 years

V&VBeginnerCurrently used1 years

Vendors&Parts (MRP system)ExpertCurrently used1 years

Visual BasicBeginnerCurrently used1 years

Visual Basic for ApplicationsIntermediateCurrently used3 years

Windows 9X/3.X/NTExpertCurrently used7 years

WordExpertCurrently used6 years

Zylux LuminometerExpertCurrently used1 years

Brachytherapy methodologyIntermediateCurrently used1 years

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WarmBlood Imports / Horse Imports http://www.warmbloodimports.com &

http://www.horseimports.com- Our services include:

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