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Metro location and a generic QA title increase competition, niche DICOM/V&V requirements partially reduce it.
High because DICOM, medical imaging workflows, and regulatory V&V require strong domain-specific experience.
High due to explicit 10+ years requirement, mandatory healthcare imaging experience, and regulatory V&V demands.
Plan, design, and execute manual test cases for healthcare software focusing on DICOM workflows, medical imaging annotations, and system interoperability.
Perform system, integration testing, and Verification & Validation (V&V) compliant with medical device regulations including FDA and HIPAA standards.
Collaborate with product, development, and clinical teams to validate system behavior, ensure regulatory compliance, and mentor junior QA engineers.
10+ years of hands-on manual testing experience.
6+ years of experience in healthcare or medical imaging domain.
Strong knowledge of DICOM standards, annotations, medical imaging workflows, and V&V processes for regulated environments.
Experience with hardware setup and configuration testing; knowledge of hospital information systems (EMR/EHR, HL7, HIS/LIS/RIS).
Deep domain expertise in healthcare software testing and medical imaging, including clinical workflows and regulatory compliance.
Experience working in regulated healthcare environments involving FDA and HIPAA requirements.
Proven ability to handle complex test planning and execution, interpret clinical data, and provide technical guidance to junior team members.