Project Manager Test
Resume:
Manuela Olaya
Professional Summary
. Experienced in Software Development Life Cycle (SDLC), Manual Testing,
White Box and Black Box Testing, Validation and Verification testing.
. Experienced in testing Software, Web Applications, System Components, and
Database
. Experienced in System Performance, Unit, Functional, Regression,
Integration and User Acceptance Testing.
. Participated in writing and implementing Test Plans, Test Cases and Test
Scripts/Protocols and Traceability Matrix. Executed Test
Scripts/Protocols and documented Test Results. Edited and re-tested Test
Scripts/ Protocols and signed off (Pass/Fail)
. Participated in Requirements gathering, Code Reviews/ Walk Trough.
. Hands-on experienced in Automated Test Tool -Mercury Win Runner, Load
Runner and Test Director.
. Created defect tracking (manual repository), maintained and updated
defect statuses and timelines.
. Exposure in Risk Assessment and Testing Methodologies.
. Exposure in FDA, IEEE, SEI, Six Sigma, ISO standards and regulations.
. Hands on use of LIMS, Trackwise, ePAS, DMS (Data Management System),
Documentum EDMS, Citrix, AMM (AS/400), Citrix and Cognos, HL7 - Logix
OE, Logix OE, Documentum.
Technical Experience
Testing Platforms:
. Windows NT, Windows 95/98, Windows 2000, Windows XP, Windows Vista, UNIX
(Sun Solaris), PC Mainframe
. PC Anywhere, Lotus Notes
. Oracle, SQL and DB2 database
. IIS Service Packs, Apache, Lynix
. MS Word, Access, Excel and Power Point
. Java, C++, Visual Basic, HTML, XML, Java Script, Pearl, ASP, APIs, EDI
. Laboratory Information and Management System (LIMS), Cognos SQL Database
Languages: HTML, Java Script, Java, Visual Basic, VB Script, C/C++, COBOL,
Assembler, Systems Analysis and Design
Databases: SQL Server, Oracle, Sybase, DB2,
Platforms/Tools: Windows NT, Windows 95/98, Windows 2000, Windows XP, UNIX
(Sun Solaris), Win 2000 Server, Win2003 Server, Oracle and SQL,
Visio, Excel and Access
Mainframes: DOS/JCL, DOS/VSE, VSAM
Testing Tools: Weblink Validator, Bugzilla, JIRA (Defect Tracking)
Professional Experience
On Site QA/ QC (Field Technician) Carefusion/ Adecco
January 2011 -Ongoing
Product Release / Finished Product Implementation
Software/Firmware Installation and Upgrade - Alaris IV Infusion Pump
Modules (Medical Device)
End Clients: Elmhurst Mem. Hospital, Alexian Brothers, Advocate Condell
Med. Center, St Alexius Hospital, Advocate Center-Lutheran, Christ
Hospital, Good Shepherd, IL. Masonic Childrens Memorial, Cook County Hosp.
(various hospitals)
. Performed test of Software/ Hardware/Firmware interface (wireless
communications) of Alaris medical device products for conformance to
specifications such as data sets, tolerances, calibrations,
deviations, scales, pressures etc. and other customer's requirements.
Ensured results conforms with specifications.
. Performed Installation Qualification (IQ), Operations Qualifications
(OQ), Process Qualifications (PQ) Validation and Verification of
protocols, test procedures and documentation of test results for
device and software conformance to specifications and requirements to
justify that Device is safe to use.
. QA Analyst, Savo Group
06/2009 - 08/2009
E-Commerce (Sales and Marketing Asset Management web based
software)
. Wrote/ Authored Test Cases/ Test Protocols based from Functional
Requirements
. Executed Test Cases/ Test Protocols. Pormed front end and back end
testing life cycle for web applications - Functional, Regression and
User Acceptance testing. Performed Data Setup, Execution of Test Cases
- Usability, Functional, Regression and User Acceptance testing in
earlier and later versions of IE and Firefox web browsers.
. Reported, reproduced and managed bugs into JIRA bug repository.
Monitored bugs till closures.
. Worked closely with Test Lead and the team to resolve issues found.
. Updated Test Cases per new requirements and enhancement requests.
QA Analyst, Walgreens Headquarter, Deerfield, IL
06/2007 - 10/2008
E-commerce (web-based)
. Responsible for verifying that the applications meet functional,
technical and design requirements. Ensure all department systems meet
organizations standards and end-user requirements. Ensure that section
508 is implemented (for low vision impaired)
. Assists with testing efforts in hosted/ multi platform environments -
Test Cases/Scripts creations and execution.
. Performed Functional and integration testing for embedded software
(credit card processing)
. Performed Functional, Regression, System Integration, User Acceptance
and Usability testing for enhancements, new programs and patches in
staging and pilot / production environment in English and Spanish site
based from Business Requirements. Maintained test results into
Bugzilla (defect tracking) and issues lists - Pass/Fail
. Performed Functional, Usability, Regression, User Acceptance testing
on Email Campaigns, Daily and Weekly Marketing campaigns,
Prescriptions (Rx) - Medicare Part A and Part B (Hipaa compliant)
. Composed clear and informative defect reports into Bugzilla. Ensured
defects are fixed in timely manner.
. Assisted in risk assessment, managing and maintaining release issues
lists till closures. Follow up with the support and development team
in diagnosis and correction of the problem.
Baxter Healthcare - Deerfield IL
1/2007 - 3/2007
Systems Validation Engineer- Clintec Nutrition, Medical Delivery - Medical
Device (Phase ll)
Logix OE, Logix CM, HL 7
. Participated in writing or re-writing of Protocols based from Change
requests. Routed Protocols for approval.
. Participated in setting up test environment/ system configurations,
Server/ Client in test machines to perform functionality Ad Hoc (black
box) testing based from functional and design specifications.
Identified root cause of issues found.
. Performed Regression Testing,User Interface and System Interface
after code fixes/ build (new install/ new build) in HL7 environment.
Run SQL Queries to pull out data in HL7 environment, verified
referential integrity from the generated reports and analyzed output
labels vs. equations, algorithm, formulas and deviations. Reported and
communicated issues to Team Leads and recommended for fixes (for
conformance).
. Participated in the design and execution of systems stress testing
(multi-users) and facilitated feedback to developers and engineers to
resolve issues.
. Responsible for the majority of GDP reviews (audit) of the entire
system Validation and Verification, ensure that system and process are
in compliance with FDA regulations -GMP, CGMP, GAMP, GXP, QSI, 21 CFR
Part 11 and CFR Part 820.
. Executed IQ (Installation Qualification), Operational Qualification
(OQ) Performance Qualification (PQ) Protocols/ Test Scripts. Verified
test results conform with specifications (expected results).
Documented test results to justify that device is fit to use.
Abbott Laboratories, Lake County, IL
12/2005 - 11/2006
Validation Analyst (Tester) GPO Projects
(Multiple Projects)
PCA Data Migration - Product Complaints Data Verification (Data Migration
Testing)
Integration/ Testing
. Updated /Edited existing Test Cases/ Test Protocols based from
Modification Requests (MRs)
. Routed Modification requests (MRs) for approval
. Created Data Setup/ Filters to be used for data queries in Cognos
Database
. Ran SQL queries to obtain reports (Ex: Search by Complaint QA
Received)
. Performed Database Migration Testing. Executed Test Cases /Protocols
and logged and documented test results - Pass/ Fail and signed off.
Reported defects to developers for fixes and updated status matrix.
. Verified reports against Complaint Data Upload spreadsheet (DataMart)
in each sites for any inconsistencies.
. Facilitated feedback and recommendations to Project Manager for any
inconsistencies/issues found (test result/ test cases) and resolved
them.
. Updated test matrix to reflect test status. Communicated with the
approvers to ensure test cases are approved and timelines are met.
LIMS Support - ABL Calculations Qualifications
. Manually calculated Assays to verify if calculated results match
system generated results and to justify that system formula are
consistent. To be incompliant to CGMP, generated reports to justify
that system generated results matches with manually calculated result
. Worked closely with System Owners and users to verify formulas
consistency
Product Complaint Analysis (PCA) 3.2
Unit/ Functional Testing
. Performed Unit Test in PCA Investigation Form for each sites (done in
Lotus Notes) - Executed Test Cases and logged test results in defect
tracking tool.
. Ran SQL queries to verify Investigation form matches with translated
fields within the SDD_PCA_GWD_Translation Matrix (in Packet Tracker).
Communicated with the team if issues are found and recommend them for
fixes.
. Performed functionality/regression test after code fixes (black box),
updated requirements tracking tool to reflect test status and signed
off (pass/fail).
Validation Analyst - Thermo LIMS Release 4.0 (Global Pharmaceutical
Operations)
. Reviewed SDLC documentations, System Components and Prototypes.
. Reviewed functional requirements, and process flow requirements,
Quality System Regulations, GMP, CGMP. GAMP.
. Authored Process Flow and Validation Protocols (wrote test cases and
test scripts) based from the user-defined requirements, implementing
21CFR part11 and CFR 820.
. Routed Validation Protocols to approvers and monitored them to ensure
they are approved in timely manner. Val Protocols stages -
Authoring, Review and Approval are managed using Documentum - check in
/ check out.
. Performed Functional Test (black box) - Ran protocols/ test cases and
communicated with the developers and team to update test results; made
sure that the requirements are successfully met and issues are fixed.
. Dry ran (peer review) Protocols and identified issues for fixes.
. Closely worked with Project Managers, Developers and System owners,
Team Leads and the Test team to discuss business process, project
updates, timelines, and open issues and resolved them.
. Performed Regression test after code fixes and updated test reports
and traceability matrix.
Validation Analyst/QA - Global Pharmaceutical Operations - QDMS
. Reviewed QDMS application functional requirements, SOPs and other
documentations
. Wrote/ Authored Validation Protocols (Test Cases and Test Scripts)
based on the requirements
. Performed Functional test (black box) and maintained test tracking
status.
. Worked closely with Developers and Validation lead to discuss project
updates, timelines and made sure that requirements are successfully
met and issues are communicated and resolved.
. Performed Regression testing after code fixes and updated test report.
BAXTER HEALTHCARE, Round Lake, IL
3/2005 - 5/2005
Quality Internal Auditor -Field Force Complaints Investigation - Hematology
- Blood Separator
Medical Device (CAPA)
. Reviewed Field Force customer complaints database (JCL/DB2),
. Performed internal audits/investigation and risk analysis against
reported complaints.
. To be incompliant with FDA regulations such QSR, GMP, CGMP, GAMP,
21CFR part11 and CFR Part 820, ensured that all issues are being
addressed and protocols are being followed.
. Ensured that system and process are in conformance with Manufacturing,
Service and Design documentations, against the applicable Baxter
Standard Operating Procedures and Regulations SOPs.
. Participated in creating and updating tracking complaints spreadsheet
for Blood Separator Medical Devices, logged Corrective and Preventive
Actions for quality improvements (CAPA).
. Participated in creating overall reports (excel spreadsheet) to
justify that non conformance -device or procedural is below the
acceptable deviations (below 2%)
Abbott Laboratories, Lake County, IL- ADD - FDA Regulated
5/2004 - 12/2004
Technical Writer, Quality Systems P-42 Reference Material DMR Remediation
. To be in compliance with FDA regulations such as QSR, GMP, CGMP, GAMP,
21 CFR Part 11 and Part 820, participated in writing and editing
Change Requests (CRs) for ADD products in different platforms.
. Routed CRs for approvals in ePAS. Monitored CRs to ensure they are
approved in timely manner (Documentum check in/ check out)
. Run queries from databases (CAPA, LIMS, AMM and DMS) in order to
write Specification Justification Packages and Selection Plan.
. Reviewed SOPs, TMVs, TMAWs, SCPs, TCPs, STPs and PSCPs documentations
and indentified issues that are found. Wrote documentations Change
request received from various departments or organizations. Interfaced
with Cross Functional Teams (CFT), SMEs, to resolve issues set
priorities and timelines.
. Facilitated Statistical Analysis report based from Input/ Output
acceptance criteria, historical data and documentations.
. Created project tracking sheet to facilitate project status and
timelines to the manager.
(routed, approved/unapproved CRs)
Environment: Windows 2000, Lotus Notes, LIMS, DMS, ePAS AMM, AS400, JCL,
DB2
Abbott Laboratories, Lake County, IL - ADD - FDA Regulated
3/2004 - 5/2004
CAPA/ Material Review Technician - Team Lead
. Primary point of contact on MRT group projects- internal audits (CAPA)
. Coordinated with Managers, System Owners and CAPA Board to understand
potential Quality problems, business specifications/ requirements and
timelines.
. Delegated MRT work to the group, set up timelines and priorities,
interfaced with Cross Functional teams to discuss project status,
issues and deliverables.
. Opened CAPA Ticket of Non Conformances in Trackwise System. -
Corrective Action / Preventive and Justification Reason as an
Objective Evidence. Monitored and communicated all submitted Ticket in
trackwise to ensure they are approved in timely manner.
. Wrote EDCs - Non Conformances including Deviations, Procedural
Errors, Non Procedural, and Risk Eval. -Product Impact and Non Product
Impact - Corrective Action / Preventive Action using Trackwise.
. Used Trackwise to write Change Requests for CAPA documentations (DMS,
Smart Form) to update libraries. Routed Change requests for approval
and ensured they are approved in timely manner.
. Created project status matrix to facilitate timelines and project
status report to the manager
Environment: Windows 2000, Lotus Notes, LIMS, DMS, ePAS AMM, DMS, CAPA/MRT,
CORE and EDC (i.e. M428, A509, M150), AS400, JCL/DB2, Trackwise
Abbott Laboratories, Lake County, IL - ADD - FDA Regulated
9/2003 - 11/2003
QA Specialist - Quality Systems Initiative - CAPA- 4
. Calculated probability analysis of Test Method Application Worksheet
(TMAW) according to the Test Method Assessment of Validity Criteria
(Doc. B563). Identified products that did not meet the default of
invalid rate of 2%, now in DMS production form 05165.
. Reviewed LIMS and Non LIMS historical data and generated Test Summary
Report for passes, Fails, No Tests and number of Runs in a particular
Test Specs.
Environment: Windows 2000, Lotus Notes, LIMS, DMS, ePAS AMM (AS/400)
Abbott Laboratories, Lake County, IL - HPD - FDA Regulated
1/2003 - 7/2003
Test Engineer - Manufacturing Engineering
Beckman LIMS (Laboratory Information Management System) upgrade designed to
schedule and track laboratory information on samples taken by EC and BQA
Laboratory with the intent of implementing 21CFR Part 11 - Electronic
Signatures and CFR Part 820.
. Reviewed User's Software and System requirements - Functional
Requirements Specification (FRS), Detailed Design Specification (DDS),
Quality System Regulations, (QSI), Standard Operating Process (SOP),
Good Manufacturing Process (GMP), GAMP, and Traceability Matrix
stored in QDMS and Trackwise .
. Participated in Beckman LIMS, LDBMS and Crystal Report trainings.
. Participated in reviewing, modifying and execution of protocols (test
cases) that comply with FDA 21 part 11 standards - Installation
Qualification (IQ), Operation Qualification (OQ), Performance
Qualification (PQ)
. Executed Test Cases and documented Test results (Pass/Fail) Wrote
exceptions on issues found.
. Wrote Test Protocols (test cases) and test scripts (test steps) for
Phase 11 testing and route them for approval.
. Modified Traceability Matrix to reflect test status.
. Performed Functionality and Regression testing. Validation and
Verification of Test Cases, Test Scripts, make sure that Test
Objectives are successfully met. Interfaced with the team to resolve
issues/ defects.
Environment: Windows NT/2000, LIMS, LDBMS, Oracle, Crystal Report
Exodus Communications Inc - (E-Business)
3/2000- 5/2001
Internet Data Center Infrastructure/ Network Monitoring
. Acted as a team Lead in Data Center Monitoring. Responsible in
creating resource schedules. Ensured that Data Center is staffed 24/7
. Performed Network Monitoring for normal performance of servers,
network components, firewall, and applications while customers are
shopping on-line.
. Performed Network Monitoring for normal performance of servers,
network components, firewall, and applications while customers are
shopping on-line.
.
. Maintained Analysis Report- Response Time, Bottlenecks and Batch file
execution, etc. Interfaced with Network Engineers if issues are found
- Network or Application specific.
Senior QA Analyst ( QA Lead) - Internet / Intranet, Applications, System
Testing - Web Testing
Web-Based applications testing for B2B, B2C commercial Websites (shopping
Cart) - Compatibility, Configuration, Visibility (Look and feel),
Functionality, User Interface, Regression, Integration and User Acceptance
Testing, System, Firewall, and Version Controls.
. Primary contact in all testing efforts, provided Test Schedules, Time
Estimates and Resources to Project Managers and Marketing Team.
Monitored testing efforts for completion till closures.
. Participated in requirements walkthrough- Design, Technical, and
Functional specifications, raised issues about timelines and
deliverables vs. budget.
. Participated in creating Test Plan, Test Cases/ Test Conditions and
Test Scripts from business requirements. Executed Test Scripts logged
and documented test results in defect Tracking Tool. Tests executions
are done earlier and later versions of IE, Netscape and AOL.
. Performed Sanity Test in System Components and Application, and
Embedded Software (middleware). Performed Functional testing,
identified and reported issues found to developers. Performed
Integration /Regression after code fixes. Tests are done in staging
environment. Performed Users Acceptance Test before modules are moved
to production. Performed Beta Test in production environment. Defects,
severity, priority/ timelines and documentations are maintained in
Defect tracking Tool. Made sure that defects are fixed and re-tested.
. Performed White Box and Block box testing and Validation Test, ran SQL
queries to test and verify referential integrity of the database vs.
schema and data model and e-mail confirmations. Analyzed test reports
and produced documentations.
. Worked closely with Project Managers and Developers and Business
Analyst to discuss test status, open issues, defects for fixes,
timelines, budget, deliverables, risk assessments, and possible
solutions.
. Assigned priority and severity to defects
Environment: Windows NT, 98, 2000, UNIX (Sun), Web Browsers, Source Safe
Version Control, IIS Service, Web Security Controls, Firewalls, Client/
Server, Development Tools: C++, Java JEE, Java Swing, HTML, XML JavaScript,
ASP Pages, Java2, Ms SQL, Oracle and Active Directory servers.
Involved in the following Projects/ Websites as a QA Analyst
. Spacesavers.com - Shopping cart applications, Addiction Solution.com
- Medical applications, Wasso.com - Sports applications,
Fobpaper.com - Shopping cart applications
. KPMG.com / Cisco - Communications Solutions, Cooleh.com - Shopping
cart applications (URL changed after development), Broadcloud.com -
Shopping cart applications
Johnson Controls, Milwaukee, WI - Manufacturing Engineering
10/1999 -12/1999
QA Analyst - Software and System Testing
Test Analyst - Migration Testing using an existing Directory server from
Win NT 4.0 Service Pack 3 to Win NT 4.5 Service Pack 5 - Web-Based
application (Intranet), GUI-testing, Black Box and White Box Testing,
System Testing, Unit (Functionality), Regression, Integration, User
Acceptance Test and System Testing.
. Reviewed requirements and goals from End User's perspective, make sure
that both software and system upgrade are working and they are Y2K
compliant.
. Reviewed System and its network Architecture (Topology), Dataflow
Diagrams and Schema.
. Initially developed/created and implemented Test Methodology using
Matrix (Matrices), Test Plan, Test Cases, Executed / Validated and
documented test results (pass/fail).
. Tested software's functionality release 1.2 (before upgrade) vs. its
system, and subsystems, an intranet-based Global Directory that holds
40,000 Johnson Controls employees.
. Coordinated with Manager and developers, identified problems and
suggested alternatives
. Tested Software and System upgrade release 1.3 after enhancements/code
changes, system's new components to make sure that software still runs
the way it should be and didn't introduce side effects.
Environment: Windows NT, Cisco, LDAP, SQL server, Oracle Server Development
- Ms Visual Interdev, HTML, Java Script, VB Script, ASP pages, C++ and Java
Harris Bank, Chicago, IL 7/1999
- 8/1999
Web Tester / Software
Internet Banking System (mbanks PC banking, Cash Flow) Web and GUI - based,
in
Client/ Server, and mainframe database server
. Tested the Homepage and it's links and hyperlinks for browser
dependencies (Netscape, IE and AOL)
. Tested input controls, applications, forms, cash flows, deposits,
withdrawals, money market, etc. are transmitted in the Mainframe
Database - DB2 via Embedded Software written in EDI.
. Generated test data to immolate end user interface, to test if
information keyed by a bank customer could be captured via On Line
System (web) and transmitted via Batch System in the backend (remote)
an EDI software, which subsequently merged and accessed internally
using DSW as the main host (vended by ALLTEL).
. Generated SQL queries to test if data were transmitted to the database
and to test software and system interface (front end and back end) and
report generation.
. Tested Transitions test dates (system generated dates if they are Y2K
compliant).
. Validated forms, created and executed Test Cases/Test Scenarios, Test
Scripts, logged test issues in a defect tracking tool and reported
them to managers and developers for fixes.
Environment: Windows NT, IIS Service Packs, CICS, EDI Development - HTML,
Java Scripts, Visual Basic, Java,
DSW (EDI imbedded program)
CCC Information Technology, Chicago, IL
3/1999 - 4/1999
Software/GUI Tester/QA
. Reviewed input and output requirements (data types), Tested GUI
controls/ Screen based input controls.
. Generated test data to execute and test the user interface versus
existing matrices and deliverables to ensure correct functionality.
. Executed Test Scripts and documented results (Pass/fail). Maintained
test results documentations in Lotus Notes.
. Run SQL queries from the Data Flow Diagram, Schema to test referential
integrity of the database. Validate results (pass/ fail)
Lucent Technologies / IBM Global Services, Lisle, IL
7/1998 - 11/1998
Software/System Tester - Manufacturing Engineering
Product: Focus Prime (Product Realization Integrated Manufacturing
Environment)
(A system that communicates with the assembly of circuit packs of a wired
telecommunications).
Achieving SEI-level 3 assessment in Software Engineering (Software
Development)
Release 3.0.0 'C' code with imbedded Sybase SQL using 'Unify Database'
Release 4.0.0 'C++' code with imbedded O2 SQL 'Object Oriented SQL'
. Reviewed requirements from the Test Specifications, Modification
Requests /Enhancements.
. Participated in Writing and Maintaining Test Plan, Test Cases, Test
Procedures from the Test Specifications before and after code fixes
(builds) enhancements.
. Performed Functional Test (black box) on the entire system using Lab
View. Reported bugs/ issues to project manager. Performed Regression
Test after builds, ensured that the entire application and its
dependencies (modules / functions), system and subsystems still run
after code fixes, modifications/enhancements.
. Run SQL queries from Data Flow Diagram, Treads, and Schema to test
referential integrity of the database if maintained.
. Coordinated with Developers, Project Mangers, and Test Leads to
discuss code problems, reported test status, and time estimates.
. Validated and documented Test Conditions and Signed Off Results (Pass/
Fail)
Environment: UNIX Sun Solaris, Windows NT, Windows 95, Microsoft Office 97,
C++, Sybase SQL, Object Oriented SQL (NOVEL)
Northrop Grumman (Bill of Material /Configuration Management), Rolling
Meadows, IL 6/1997 - 7/1998
Database Migration/ Maintenance
. Participated in Data Migration of a Manufacturing Engineering
application. Investigated online system and its functionality if it's
working after the migration.
. Prepared Bill of Materials from various information sources for a
procurement of Manufacturing and Engineering of DSD products to fully
document production in order to provide visibility of assemblies and
piece parts in their proper position and location.
. Maintained DBMS files using PC Pro for Bill of Materials, PWB and CAD
drawing Modifications
. Created DBMS (an inventory database) for transition software using MS
Access
Environment: Lotus Notes, CICS, Assembler, C/C++, and MS Access
UNISYS, Oak Brook, IL
5/1996 - 6/1996
Quality Control Clerk Online GUI System (Hardware/Software - Shipping)
. Participated in migrating database from EDI Tracking System into
UNISYS client server using Excel, PC Pro, Microsoft Word and Maper
(Internet) in UNIX platform. These applications were being used to
transmit and update information.
Environment: UNIX, EDI, UNISYS, MAPER (WEB), PC PRO, and Windows 95
Abbott Laboratories, lake County, IL - FDA Regulated
9/1996 -10/1996
Manufacturing Engineering
Software /System Tester - Medical Device to test blood impurities
GUI Testing - Functionality, Regression, Integration, Users Acceptance and
system interface
Responsibilities:
. Reviewed User, Software and Hardware specifications and
documentations.
. Performed manual and automatic test to emulate blood samples and to
generate Assays,
. Tested instruments interface in different platforms - FPC 2.0, PPC
8.0, BBS
. (Instruments to test blood impurities like HIV)
. Tested System Configurations and Applications interface - Menus, Sub
Menus/Pop up Menus, Screen Controls and DBMS.
. Executed Test Cases (home grown), Test scripts to test User's vs.
System Interface that comply with FDA 21 CFR part 11 standards.
Interfaced with test coordinators and developers to discuss open
issues. Documented results (pass/fail) and Signed Off.
Environment: UNIX, C, and C++
MFS Telecommunications, Oak Brook, IL 8/1996
- 9/1996
Software Tester, User Acceptance Testing (UAT)
MFS acquired a Telecommunications CO. at that time and they both merged
their Billing System using MFS System and platform. The program was re-
coded from C to C++.
Responsibilities:
. Involved in Data Migration of Billing System into MFS platform
. Manually generated test data to create database (End User's environment)
and to test referential integrity of database is maintained. Test Keyed
billings using different iterations (scenarios) to test system vs.
software interface (after code changes). Coordinated with developers to
report and discuss problems.
Environment: UNIX, C, and C++
Education:
Bachelor of Science in Business Administration
Business Administration Major: Economics
UNIVERSITY OF THE EAST Manila, Philippines
COLLEGE OF DUPAGE, Glen Ellyn, Illinois (in process)
Major: Applications Programming (C, C++, Java, VB, WEB - HTML, Java
Scripts)
Network Administration - Windows NT, Windows 2000, Professional and
Advanced Server,
Directory Server and Security Network (for MCSE Certifications)
Training (Ongoing)
HP Automated Test Tools: QTP, Quality Center
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