Verification and validation
Each requirement and risk control has a test, a result and a sign-off that can be traced.
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In clinical and device software, testing is part of the regulated record. QA here means verified requirements, documented risk controls and evidence an auditor can follow from a hazard to a passing test.
Reply within one working day. NDA before we see your backlog. Shortlist in about 4 working days.
The risks that matter most in this industry, and the checks we put in place for each. Engineers are matched on these, not only on tool names.
Each requirement and risk control has a test, a result and a sign-off that can be traced.
Role-based access, audit trails and de-identified test data for protected health information.
HL7 v2 and FHIR messages exchanged with hospital systems, labs and devices, tested against real-world payloads.
Hardware-in-the-loop tests, alarm handling and fail-safe behaviour on embedded devices.
Each role links to the hiring page and to the role guide. Pay shown is the US median for mid-level, gross per year.
Owns the verification plan and audit trail.
Traces requirements to risk controls and tests.
Test protocols and validation reports.
Regression for clinical web and mobile apps.
Usability for patients and clinicians.
We staff 15 QA roles in every industry. Tell us the one you need and the stack it runs on.
All QA rolesTools common in healthcare and MedTech QA. We staff against your stack, so this list is a starting point and not a limit.
Each tool page shows demand, pay and a learning path. Licences stay in your name.
These standards describe obligations that usually apply to the product or the client. PassRidge does not hold them on your behalf and nothing here is legal advice. Your compliance owner sets the scope.
US rules for protected health information, including access control and audit logging.
The software life-cycle standard for medical device software, including verification and the software safety class.
Quality management for medical devices, and risk management applied to them.
Requirements for electronic records and signatures, which testing must cover for systems that keep them.
The European medical device regulation, which includes software as a medical device.
Our engineers work inside your controls, on masked or synthetic data, and produce test evidence in the format your reviewers ask for. How security works in every engagement.
Evidence, strategy and traceability are a service you want one accountable owner for. It is a starting recommendation: all five models are available for healthcare and MedTech work.
We run QA end to end and report against agreed SLAs.
Add vetted QA engineers to your team, under your management.
A stable QA squad that works only on your product.
Fixed scope, fixed price: a release tested, an app audited.
Real listings with pay shown. Looking for a job in this industry? Browse them all.
Our regulated-industry testers have worked inside those quality systems and follow your procedures. We do not hold your device certification. Your quality system stays yours.
We do not need it. Test environments should use de-identified or synthetic data. Where access to real data is unavoidable, we sign the agreements your privacy officer requires and restrict access to named people.
Yes. Technical writers and business test analysts write test protocols, execute them and produce summary reports in your document templates.
Usually managed qa (qaaas). Evidence, strategy and traceability are a service you want one accountable owner for. Managed QA (QAaaS) starts in about 21 days, mid-level rates begin at $48 an hour and the minimum term is 6 months. The five models are compared at /outsourcing/.
Send the product, the stack and the release cadence. An engagement manager answers with a team outline, a recommended model and a price range.
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