Client: Zensar

Experience: 8-12 Years

Location: Hyderabad.

Responsibilities:

• You should have BS or equivalent degree in math, science or engineering
• At least one-year experience in software testing, preferably in FDA-regulated environments
• Familiarity with 21 CFR 11 and Annex 11

Technical Skills required to contribute:

• Operating System: Windows and UNIX.
• Languages: SQL, SQL*Plus, HTML, XML, Java Script, ABAP and TSL
• ERP: SAPS/4HANA
• Development Tools: Visual Basic, Power builder and Developer2000.
• Software Packages: MS Word, Excel, Power Point, Outlook, Frame maker, Internet Services Automated Test Tools: QTP, Quality Center, PVCS Tracker 6.0 & Continuous.
• Internet Technologies: Internet Basics, HTML & Concepts of Networking

Responsibilities 

• Performed end to end validation process for One Pharma project (Blue print to Go-live) in SAP S/4HANA
•  Developed validation Plan for One SAP Project, CSV Risk Assessment, Summary reports and Traceability Matrix.
• Developed validation protocols based on SOP's - IQ, OQ, PQ 
• Developed Test Scripts in SAP QM, BW, MM, SD and FI/ Confidential modules.
• Interacted with Functional, Development Team to develop Test Scripts according to the requirements and Business Print Procedure.
• Validated BPP's, URS and FRS as per GMP.
• Involved in Unit Test, Integration, Regression and UAT.
• Using Master date to create data sets for test and validation process.
• Validated RICEF as per BPP specifications.
• Performed pre & post approval reviews for SAP test scripts:
• Reported the defects in HP Quality Center and involved in Regression Testing.
• Conducted Audit trails - 21 CFR part 11 for GMP.
• Involved in Test script development and data validations.
• Used SAP solution Manager and Documentum for document management.
• Tested Reports, interfaces, Conversions, Enhancements and Forms.
• Worked closely with Functional, Development Team to solve the defects reported in Test Director.
• Validated QTP for test automation.