Anand R. Venkinani
**** ******* **** ***** . ************, IN 46239
317-***-**** . cell 317-***-**** . abjepr@r.postjobfree.com .
abjepr@r.postjobfree.com
Quality Engineer / Validation & Test Coordinator
Articulate communicator, technical resource and forward-thinking
professional experienced with strategic planning, quality, test
management, validation vendor interface, change management, document
management, operational sustainability, disaster recovery and contingency
planning
Comprehensive knowledge of information management, testing methodologies,
data storage and analysis, software development & methodologies,
requirements facilitation, security and optimization
Certified Software Test Engineer (CSTE); Quality Center ReqPro,
ClearQuest, Team Foundation Server, RAD, RUP, Waterfall, Agile & Critical
Chain Methodologies, TOAD, SQL, Documentum, Remedy, LotusNotes
Proficiencies
PROJECT PLAN DEVELOPMENT SOFTWARE EVALUATION AND TESTING
Business Process Testing & Validation Test Script Engineering and
Execution
Risk Management and Mitigation Defects Tracking & Monitoring
Periodic Review and Business Continuity Disaster Recovery
Planning/Development
Requirements Traceability Quality Engineer-Test
Coordinator
Test Script Engineering and Execution Validation Coordinator
Technical Skills/Environment:
. HAD HANDS ON EXPERIENCE TESTING WEB-BASED, CLIENT /SERVER APPLICATIONS
THAT ARE DEVELOPED USING .NET, JAVA, PERL, LOTUSNOTES, INFOPATH,
SSIS/SSRS TECHNOLOGIES.
. Involved Testing experience with IBM Mainframes and Development
Experience using COBOL, JCL
. DB2, Oracle, SSRS, COBOL, JCL, SSIS, Quality Center, ReqPro,
ClearQuest, TFS, MS Office, CCPM, SharePoint, Informatica, Windows XP,
HTML, MVS
Experience
QUALITY ENGINEER-VALIDATION/TEST COORDINATOR: ELI LILLY,
INDIANAPOLIS, IN - JUN 00 TO PRESENT
Systems Analyst: DIS, Inc (Eli Lilly Contractor), Dallas, TX - May 97 to
May 00
. Defined business process and procedures integrating new technology into
existing infrastructure; engineered database design changes enabling
users to access critical data
and generate reports
. Identified and corrected critical program compliance deficiencies;
received prestigious Solution Achievement Award and numerous Spotlight
and Quality Advocate awards
. Coordinated validation testing for 25 R&D high risk, IT systems; lead
project teams responsible for collecting and analyzing data and
preparing project plans prior to system transitions
. Quality Engineer and project manager for numerous internal remediation
teams; created test methodologies, validation plans and detailed summary
reports
. Point-of-contact responsible for maintaining SDP website; integrated
policies, methodology and resource webpage that provides instant access
to key data necessary for quality and testing process development
. Instrumental in testing of clinical trial data test scripts in
accordance with GcP documentation procedures
. "Build to Last" team member responsible for identifying global test and
validation processes and tools; provided guidance/examples on software
test & requirements
. Guided testing teams in preparing test data. Wrote Data migration test
strategy for a complex application; Involved with review and approval of
system and performance/load tests;
. Extensive involvement with unit, integration, system & user acceptance
testing; also experienced with data migration, regression and
performance testing activities.
. Lead testing efforts for a complex and critical system that is
implemented in different zones (US, OUS) and mostly is a primary
structure drawing tool for Lilly Research scientists. Acted as Quality
Engineer and SME in regards to Testing, and other quality related
questions/issues. Worked directly with global project team operated from
US and local teams that are responsible for a particular country or site
in resolving number of issues;
. Hands on experience with requirements facilitation, design reviews,
requirements traceability and defining defects monitoring strategies.
. As part of Quality Remediation team which is responsible for auditing
and complete action items from audit, I worked with Lilly project teams
and our vendor TCS (onsite and offshore). Involved with bringing about 5
GcP (that are subjected for internal or external (FDA) audits) Systems
back to Lilly CSV compliance.
. Involved with creation, review and approval of validation documents that
includes but not limited to - Test Strategy, Methodology, Guidelines,
Test Plans, Validation Plans, Risk assessments, Test summary and
validation reports, RTM's, Support plans, Vendor evaluations, Periodic
reviews, System retirement plans, BCP, DRP documents, NTF's and Security
plans.
. Acted as Testing Point of Contact for LRL R&D IT (responsible for
solving testing related issues along with making any necessary changes
to test templates and documentation)
System Analyst: Cadalyst Info - Aug 95 to Apr 97
. Responsible for coding, testing and implementing billing system
software; provided ongoing support and systems training for production
personnel
. Involved with error log verification and work on resolving defects
. Created test scripts, requirements traceability, test metrics and test
summary reports
. Helped developers creating unit and integration test checklists. Using
that experience created UAT checklist which is kind of unique approach
for the entire Quality dept.
Education, Training and Awards_____________________________
BS: INDUSTRIAL PRODUCTION, MANIPAL INSTITUTE OF TECHNOLOGY, MANIPAL,
INDIA
Certified Software Test Engineer - certification from QAI, Florida
Solution Achievement Award
Quality Advocate Award
Multiple program management awards
References Available Upon Request