Senior QA Analyst – Biomedical IT (Remote, EST)

HonorVet Technologies; United States; Remote; USD 55.000 - 96.000; Teilzeit

Zusammenfassung

HonorVet Technologies is seeking a Senior QA Analyst- Biomedical for a 9‑month remote assignment working on EST business hours. You will coordinate seed data validation, execute end-to-end testing, and collaborate with multi-disciplinary teams to ensure software integrity in biomedical contexts.

The ideal candidate brings 5+ years of QA experience, strong JSON/XML testing skills, and familiarity with ERP-like environments, regulatory considerations, and SDLC processes in FDA-regulated settings.

Qualifikationen

• 5+ years in software QA end-to-end testing.
• Experience with JSON and XML, understands objects and syntax.
• Experience testing a complex ERP system with interconnections.
• Able to work in a matrixed, project-oriented environment.
• Biomedical IT testing experience strongly preferred.
• Excellent SDLC, risk and change management understanding.

Aufgaben

• Fulfill time-sensitive seed data requests for testing and validation events.
• Seed historical donor and donation data for complex testing.
• Use JSON files to seed test data for applications.
• Create mock records to populate test environments.
• Investigate testing issues and perform root‑cause analysis.
• Collaborate with seed data automation team on scripts.
• Communicate effectively on Teams chat.

Kenntnisse

QA end-to-end testing

JSON/XML testing

ERP system testing

Matrixed environment

Biomedical testing

SDLC knowledge

Risk management

Documentation

Team collaboration

FDA/regulatory knowledge

Deadline-driven

Jobbeschreibung

HonorVet Technologies is seeking a Senior QA Analyst- Biomedical for a 9‑month remote assignment working on EST business hours. You will coordinate seed data validation, execute end-to-end testing, and collaborate with multi-disciplinary teams to ensure software integrity in biomedical contexts.

The ideal candidate brings 5+ years of QA experience, strong JSON/XML testing skills, and familiarity with ERP-like environments, regulatory considerations, and SDLC processes in FDA-regulated settings.