QA Engineer

• Conduct quality reviews of assessments and clinical documentation completed by Nurse Assessors
• Analyze reports and quality metrics to identify trends, ensure compliance, and support operational excellence
• Utilize proprietary quality assurance tools to evaluate performance and maintain program standards
• Provide constructive feedback and guidance to clinical staff
• Gather and report data to drive program improvements and support regulatory and contractual requirements
• Help ensure individuals receive appropriate services and supports through accurate and compliant assessment processes
• Collect data related to assessments and assessment outcomes
• Complete quality audits using proprietary QA tools
• Review QA data and report on trends and scores identified through quality audits
• Analyze recommended scores in relation to Clinical Assessor determinations
• Develop and complete reports tracking and trending activities and outcomes
• May provide QA training to staff
• Perform other assigned duties

Clinical QA Analyst, LPN

• Facilitate and provide QA/QC oversight for field implementation of NLR's Construction Quality Management program and related programs and procedures
• Develop working knowledge of contract documents, plans, specifications, and applicable codes
• Review project-specific QA/QC plans, scopes of work, and work procedures
• Develop engineering procedures for document control, submissions management, RFI tracking, material samples, testing schedules, and punch-list items
• Implement project-specific QA/QC plans in coordination with project safety plans
• Establish relationships with Site Operations, architects, consultants, subcontractors, and vendors
• Coordinate Quality Control procedures with project execution plans and schedules
• Improve strategies and tools for documenting, tracking, and recording compliance
• Facilitate third-party inspections and testing; analyze and report results
• Oversee punch lists, corrective work, project close-out, and quality reports
• Monitor, assess, trend, and report management systems data
• Participate in ESHQ assessments, readiness verifications, inspections, and essential meetings
• Plan, perform, and coordinate ISO assessments, DOE surveillances, self-assessments, and observational monitoring
• Lead or support corrective actions and causal analysis resulting from investigations and assessments
• Manage, verify, and perform effectiveness reviews for corrective actions
• Identify measuring and test equipment and calibration requirements; establish protocols and track status
• Develop and disseminate best practices and lessons learned
• Develop or provide quality-related training to facility operations staff
• Support configuration management, change control, and facility maintenance management processes
• Contribute to lab-wide quality process development, implementation, and improvement
• Provide quality assurance for Integrated Safety and Management and Environmental Management Systems
• Review and verify training and qualification records for staff and subcontractors
• Support special projects and initiatives led by the ESHQ Office

Quality Assurance Professional IV

• Improve strategic suppliers' quality performance for Trane manufacturing sites and final customers
• Ensure compliance with the Global Supplier Quality Manual under the Trane Technologies Business Operating System
• Provide servant leadership for the supplier corrective action program
• Increase tool usage across sites and improve efficiency and effectiveness for non-conforming material, return material authorization, and corrective action requests
• Provide suppliers technical oversight in process development, PFMEA, control plans, PPAP, measurement systems, standard work, and error proofing
• Coordinate initiatives between manufacturing site SQEs and suppliers for effective problem solving
• Assist in managing supplier-caused quality escapes, including on-site intervention
• Support supplier recovery initiatives involving warranty, concessions, and production interruptions
• Leverage enterprise supplier development and commodity-based expertise
• Coordinate supplier-initiated temporary or permanent change requests affecting multiple manufacturing sites
• Promote supplier quality maturity and drive applicable KPIs
• Collaborate with field quality, operations, engineering, and procurement in a matrixed organization

Regional Supplier Quality Engineer

• Design, implement, and maintain automated UI and end-to-end test suites using Playwright and TypeScript across React and Angular applications
• Write automated API tests against C# / ASP.NET Core REST endpoints, validating request contracts, response schemas, business logic, and error handling
• Build and maintain integration tests for service-to-service interactions and application data flows, including SQL Server / Azure SQL validation
• Design repeatable, isolated test data setup and teardown for reliable parallel test execution
• Use AI-assisted tools such as GitHub Copilot and Claude to accelerate test scaffolding and generation
• Critically evaluate AI-generated tests for coverage completeness, assertion quality, and false confidence
• Contribute to Azure DevOps CI/CD pipelines and maintain automated suites as mandatory quality gates
• Identify, document, and track defects in Jira with reproduction steps and test evidence
• Participate in sprint ceremonies, test planning, risk assessment, and acceptance criteria definition with the Technical Product Owner
• Partner with offshore QE engineers to scope test cases, provide review feedback, and maintain shared quality standards
• Report to the Manager, Quality Engineering

Quality Engineer, AI-Native

• Lead and develop a team of quality engineers, automation engineers, and testers
• Set team priorities, goals, and expectations aligned with delivery and quality outcomes
• Drive AI-powered design, generation, maintenance, and execution of automated tests across API, UI, integration, and end-to-end workflows
• Evaluate and implement AI-assisted capabilities to improve automation speed, coverage, stability, and maintainability
• Establish standards and guardrails for responsible AI use in test development, execution, and defect analysis
• Guide AI use for regression optimization, defect triage, failure analysis, and test maintenance
• Lead improvements to automated test frameworks and coverage
• Stay hands-on with automation design, AI-assisted test generation, framework decisions, and workflow improvements
• Improve regression strategy based on product risk, release timelines, and quality goals
• Partner with engineers to embed AI-enabled automation and quality practices earlier in the development lifecycle
• Support release quality processes, including test readiness, defect review, regression status, and go/no-go input
• Identify quality risks and escalate issues with recommendations and supporting data
• Define and track quality metrics, including automation reliability, regression effectiveness, escaped defects, release readiness, and defect trends
• Use data to prioritize improvements and communicate quality health to leadership
• Report to the VP/Director, Engineering

Manager, AI-Native Quality Engineering

• Develop and maintain comprehensive strategies for risk management activities
• Collaborate cross-functionally to ensure product quality and patient safety
• Create and maintain the risk management file, including plans and reports, and conduct regular risk reviews
• Lead hazard and risk analysis activities to identify potential risks and implement risk controls
• Lead Design Failure Modes and Effects Analyses (DFMEAs) with project teams
• Analyze and review product complaints to anticipate and prevent future issues
• Integrate product security measures addressing potential vulnerabilities into the risk management file
• Participate in Process FMEA/User FMEA development and integrate them into the risk management file
• Lead design reviews and maintain the risk management file throughout the product lifecycle
• Develop and manage post-market surveillance plans
• Lead field issue evaluation during initial launch, including root cause analysis, risk evaluation, and product containment strategy
• Ensure traceability between the risk management file, requirements, and design outputs using a requirements management tool
• Evaluate safety risk implications of design changes
• Define and implement engineering and statistical processes supporting product quality and compliance
• Ensure compliance with FDA, ISO 14971, ISO 13485, IEC 62304, FDA Part 820, and other international standards
• Participate in regulatory audits and inspections
• Oversee design validation and design verification activities, including test plans, protocols, test methods, and reports
• Ensure thorough and accurate documentation of test results, risk assessments, and reports

Risk Management Quality Engineer I – New Product Development, Surgical

• Develop and maintain comprehensive risk management strategies
• Collaborate cross-functionally to ensure product quality and patient safety
• Create and maintain risk management files, plans, and reports
• Conduct regular risk reviews
• Lead hazard and risk analysis activities and implement risk controls
• Lead Design Failure Modes and Effects Analyses (DFMEAs)
• Analyze and review product complaints to anticipate and prevent future issues
• Integrate product security measures and vulnerabilities into the risk management file
• Participate in Process FMEA/User FMEA development and integrate results into the risk management file
• Lead design reviews and maintain the risk management file throughout the product lifecycle
• Develop and manage post-market surveillance plans
• Lead field issue evaluations, including root cause analysis, risk evaluation, and product containment strategy, during initial launch
• Ensure traceability among the risk management file, requirements, and design outputs using a requirements management tool
• Evaluate safety risk implications of design changes
• Define and implement engineering and statistical processes supporting product quality and compliance
• Ensure compliance with FDA, ISO 14971, ISO 13485, IEC 62304, FDA Part 820, and other international standards
• Participate in regulatory audits and inspections
• Oversee design validation and verification activities, including test plans, protocols, methods, and reports
• Ensure accurate documentation of test results, risk assessments, and reports

• Serve as onsite quality representative on one or multiple projects under quality leadership
• Review and manage submittals during preconstruction and coordination meetings
• Verify approved submittals, materials, and installations before and during construction
• Monitor construction processes and identify and resolve quality issues
• Execute and document inspections, audits, and testing according to ITPs, project quality plans, and procedures
• Maintain accurate and current drawings, specifications, submittals, and quality documentation
• Track quality observations, deficiencies, and non-conforming work through resolution
• Coordinate corrective actions and verify completion
• Manage hold points and verification inspections
• Assist with special and third-party inspections
• Use the Quality Management System for auditing, reporting, and documentation
• Manage To-Do Lists, punch lists, and observation tracking through closeout
• Read, interpret, and apply quality manuals, inspection procedures, and project-specific quality plans
• Support corrective actions and perform other duties supporting project and quality objectives
• Indirectly manage subcontractor Quality teams and direct quality-related tasks for field/project engineers and field assistants