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Work Flexibility: Hybrid Staff Advanced Quality Engineer Portage, MI Join a team focused on advancing quality throughout the product development lifecycle in a regulated medical device environment. As a Staff Advanced…
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and…
What You Will Own: Program Leadership: Own the full NPI program from transfer through production launch — driving the integrated program plan, milestone tracking, risk management, and cross-functional alignment across…
Assess connected medical devices and digital health software for security compliance with EU CRA, FDA guidelines, and IEC 81001-5-1, guiding secure development and risk management.
Build and maintain automated tests for a digital health platform using JavaScript/TypeScript, Cucumber, and Playwright to ensure reliable releases and high software quality.
Manager, Software Engineering Location: Bothell, WA, US Employment Type: FULL_TIME Company Overview Verathon is a global medical device company focused on supporting customers by being their trusted partner, delivering…
Senior Systems Engineer Location: Bothell, WA, US Employment Type: FULL_TIME Company Overview Verathon is a global medical device company focused on supporting customers by being their trusted partner, delivering…
Designs and maintains secure medical-device systems by leading threat modeling, security architecture, and regulatory compliance for Verathon’s connected products.
Oversee medical-device laser-processing projects from prototyping to production, ensuring compliance with FDA/ISO standards and coordinating cross-functional teams to meet delivery and quality targets.
Lead quality assurance for medical-device development, ensuring compliance with ISO and FDA standards while collaborating with R&D to design and validate new products.
Maintain and improve Biocodex’s quality management system by writing procedures, tracking KPIs, running audits, and training teams on GMP/ISO standards for pharmaceutical products.
Support clinical quality assurance for medical device trials, ensuring regulatory compliance with EU MDR and ISO standards while maintaining clinical study documentation and auditing processes.
Global Supplier Quality Engineer II Location: US-NJ-Plainsboro-105-Facility, US-NJ-Princeton-100-Headquarters Time Type: Full time Job Description Changing lives. Building Careers. Joining us is a chance to do…
Build and own automated QA infrastructure using Playwright, TypeScript, and AI evaluation tools, integrating tests into CI/CD while ensuring platform reliability and compliance.
Manages technical projects for metal powder production, ensuring quality, safety, and regulatory compliance while coordinating with global teams and supporting additive manufacturing processes.
Develop and verify C++ software for real-time urology medical devices, writing automated tests and ensuring FDA-compliant documentation and risk management.
Lead the design and control of irrigation and aspiration systems for kidney stone treatment devices, integrating pumps, valves, sensors, and embedded software while ensuring regulatory compliance.
General Description: The Quality Engineering Co-op will work with Advanced Quality Engineers (AQE) and Post-Market Quality Engineers (QE) to ensure we develop the right products up front – evaluate risk, ensure our…
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