HOT REQ Urgent requirement for QA Analyst at Pea pack, NJ/Iselin, NJ

Hi,

 

Hope you are doing great!

USG direct client is looking for QA Analyst at Pea pack, NJ/Iselin, NJ

Job Title: QA Analyst

Job Location: Pea pack, NJ/Iselin, NJ

Domain: Pharma

Type: Contract

Interview: Telephonic & Skype

Experience Required: 9-12 Yrs.

Role Description:

·         9 - 12 years of experience in testing domain.

·         Documenting functional and integration requirements

·         Creation (or change of existing) RSV documents

·         RSV updates, configuration changes and related testing

·         Final Verification testing

·         Creation of all supporting documentation: technical design, installation documents, integration deployment documents, interface mapping documents

·         Strengths should include functional knowledge of various testing types & technologies, client interactions, handling teams, project planning and co-ordination of team in varied geographies.

·         Excellent oral and written communication as well as analytical and interpersonal skills.

·         Experience in working with clients from various backgrounds and at various geographical locations.

·         Expertise in QA, Requirement Analysis, Team Management, Planning, Estimations, Scheduling, and Defect Management (using ALM-QC).

·         Should have experience on Test Planning, Testing Effort Estimation and Test strategy creation.

·         Ensure compliance of all testing artifacts and processes

·         Coordination with stakeholders, BA, testing team and Quality team.

·         Provide status to program team on testing activities of on-going applications

·         Reviews and root cause analysis of testing activities.

·         Experience within a delivery role

·         Experience with client facing consulting engagements.

·         Knowledge of Pharma domain.

·         Working knowledge of performance testing and tools

·         HP Quality Center /ALM; MS Dynamics

·         Should be well versed with the Pharma domain – terminology & industry standards.

·         Should have knowledge of 21 CFR Part 11– Computer Systems Validation and other compliance processes.

Please share your updated resume at shivani.g@usgrpinc.com or feel free to contact me at 614-401-5196

 

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