Manual QA Tester

Siri InfoSolutions Inc

Chaska, MN, United States

14 days ago

Role details

Contract type

Permanent contract

Employment type

Full-time (> 32 hours)

Compensation

$110,000.0 - $130,000.0

Working hours

Regular working hours

Job source

Agile Methodology Systems Development Life Cycle Test Execution Engine Iq/oq/pq Test Scripts Integration Tests GXP

Analyze business and functional requirements and participate in requirement walkthroughs
Design, document, and execute test cases, test scenarios, and test scripts
Perform functional, system, and integration testing
Prepare and maintain test environments as per BCI/client guidelines
Log, track, and manage defects through resolution
Prepare test execution reports and communicate testing progress
Maintain validation documentation and QA artifacts
Ensure compliance with QA and validation standards and documentation processes
Support QA compliance activities and obtain required approvals for validation deliverables
Collaborate with business users, developers, and stakeholders throughout the testing lifecycle
Work directly with clients to support testing and validation activities, Position: Manual Tester Location: Chaska, MN (Onsite) Type: Fulltime Salary: $110K - $130K / Year + Benefits Must Have Technical/Functional Skills: Experience in manual …
2 hours ago, Role: Manual Tester Location: Chaska, MN FTE Only Job Description Must Have Technical/Functional Skills: Experience in manual test execution and defect tracking Ability…
7 hours ago
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Experience in manual testing, test execution, and defect tracking
Strong understanding of functional, system, and integration testing
Ability to analyze business/functional requirements and develop test scenarios and test cases
Experience with QA documentation, validation processes, and maintaining test artifacts
Experience in Medical Device/Medical Validation projects
Exposure to Tulip, MES, or Manufacturing Execution Systems
Familiarity with validation documentation (IQ/OQ/PQ, SDLC, GxP preferred)
Excellent communication and client-facing skills, * Experience with Medical Devices, Life Sciences, or Pharmaceutical manufacturing environments
Knowledge of MES platforms, Tulip applications, or manufacturing workflows
Understanding of GxP, FDA validation, and regulated environments
Experience working in Agile projects is a plus.