Manual Test Consultant [clinical/Biotech/Bio Pharma Domain is Mandator

Manual test consultant [Clinical/Biotech/Bio pharma domain is mandatory] is required to on one of our clients, a large system integrator to join their client project team based in Germany.

MANDATORY PARAMETERS

Manual testing and Clinical/Bio Pharma domain experience

JOB SPEC:

-Minimum of 8 years of experience providing Software QA and Testing services.
-Proven track record to perform all aspects of Quality Assurance, such as planning QA activities, providing input into requirements/specification/design.
-Create or support the creation of test plans, scenarios, test cases and test data, execute approved test plans and report/document results of executed test plans.
-Document and manage software defects, using a bug tracking system, and report defects to the respective team members.
-Experience in Bio pharma/Biotechnology/Clinical Research Organization is a plus.
-Familiarity with FDA regulations such as 21 CFR Part 11 and GxP desirable.
-Experience with various SDLC processes and how various QA activities and quality-centered best practices fit into such product development life cycles.
-Experience with agile software practices and managing work across more than one project.
-Experience in waterfall methodology preferred.
-Knowledge of and experience with best practices in configuration and change management of software components and packages including defect/issue reporting and tracking.
-Good knowledge of SQL is must.
-Must have knowledge of HP Quality Center 10.x or higher version.
-JIRA exposure is a plus.
-Any software testing certification is a plus.
-Manual Testing team member to manage functional, Regression, End to End testing.
-Experience working with onsite/offshore model.
-Solid written and oral communication skills in both conversational and technical English.
-Clinical logistics, Warehouse/supply management experience
-Mobile Application Testing