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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…
Lead end-to-end development and market introduction of new intraocular lenses, coordinating global teams across R&D, regulatory, quality, and supply chain to deliver compliant, patient-focused medical devices.
Leads software quality engineering and cybersecurity for a robotic surgical platform, ensuring compliance with FDA, ISO, and cybersecurity standards across AI/ML, SaMD, and embedded systems.
Intellisense Systems, Inc. is a privately held company with a proven track record of developing and deploying innovative products that successfully operate in the most extreme environments. We are a fast-growing…
QA Engineer I at a medical device manufacturer performing routine quality engineering work including risk management documentation, ECN reviews, nonconformance disposition, and quality system maintenance in a regulated manufacturing environment.
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we…
We anticipate the application window for this opening will close on - 4 Sep 2026 At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living…
Job Description Summary Under limited supervision, supports engineers in the design, implementation, maintenance, and continuous improvement of manufacturing processes, tooling, fixtures, and production equipment.…
The Senior Manager, Quality Engineering (2nd Shift) is a people leadership and manufacturing quality role responsible for providing quality and compliance oversight across second-shift operations. This leader will…
As a part of the Quality for Combination Products and Medical Devices (CP/MD QA) department, the Associate Quality Engineer will support Quality activities in global teams involved in the design, development,…
Working at Freudenberg: We will wow your world! Responsibilities: Apply quality standards to support the development, qualification and manufacturing of products to meet internal and external requirements. Apply…
Location: McMinnville, Oregon Job ID: R0143109 Date Posted: 2026-08-27 Company Name: HITACHI AMERICA, LTD. Profession (Job Category): Other Job Schedule: Full time Remote: Yes Job Description: Manager, Manufacturing…
About the Role We are seeking an experienced Regulatory Affairs professional to lead IVD (in vitro diagnostic devices) regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways…
About the Role We are seeking an experienced Regulatory Affairs professional to lead medical devices and combination products regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory…
Internal Job Description MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we…
PulseMedica is advancing the next generation of ophthalmic medical device technology, and we’re looking for a Project Manager who’s energized by complex, multidisciplinary engineering. You’ll join a team working at the…
Performs quality control inspections and tests on medical devices and components, documenting results and supporting CAPA activities in a regulated GMP environment.
Lead embedded software development for advanced medical monitors at Baxter, owning the full SDLC from architecture through sustaining support using C/C++, RTOS, and Embedded Linux in a regulated, safety-critical environment.
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and…
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