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Define and ship cloud-based Quality Management System software for regulated industries like manufacturing, medical devices, and pharmaceuticals, using Salesforce and Agile practices.
Design and execute verification tests for a non-invasive neuromonitoring medical device, ensuring compliance with FDA and CE standards across hardware, software, and system levels.
Leads QMS implementations and regulatory compliance for medical device clients using an AI-powered platform, shaping future regulatory affairs strategies while ensuring high-quality standards for life-saving devices.
Sr. Equipment Automation Engineer (Software) Location: San Jose, California Department: Operations, Manufacturing, Supply Chain Who We Are Noah Medical is building the future of medical robotics. Our next generation…
Summary The Operations Manager is responsible for leading production operations for a portfolio of electro-mechanical medical devices. This role is accountable for delivering operational excellence through continuous…
Blatchford is a multi-award-winning, global, manufacturer of some of the world’s most advanced prosthetic technology, bespoke seating solutions and orthotic devices. Our evidence-based approach and commitment to…
Architect and develop .NET/C# microservices and cloud-native apps for medical diagnostics, leading a distributed Agile team to deliver regulated software that improves patient care.
Leads software quality assurance for genomic tech products, ensuring compliance with industry standards (e.g., IEC 62304, ISO 13485) and regulatory requirements across the SDLC while collaborating with cross-functional teams to mitigate risks and improve processes.
Leads quality assurance for an automotive stamping supplier, ensuring IATF 16949 compliance, PPAP submissions, and metrology systems while driving process improvements and customer issue resolution.
Quality Engineer III at Thermo Fisher Scientific in Marietta, OH ensures manufacturing products meet FDA, ISO, and GMP standards by leading CAPAs, audits, and continuous improvement initiatives.
Define and govern the end-to-end software architecture for a new medical robotic platform, integrating robot control, clinical workflows, AI, cybersecurity, and regulated lifecycle processes.
Precision Edge Surgical Products Company LLC As a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway— you’ll be doing things that matter, leading at every level, and…
Oversee supplier process validations (IQ/OQ/PQ) for medical-device components, audit suppliers, and drive continuous improvement in a regulated healthcare environment.
The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock…
QA Engineer at a medical-device company validating and managing CAPA, risk, and change processes for laser eye-surgery systems in Teltow, Germany.
Designs and verifies next-gen medical devices for renal denervation, integrating hardware, firmware, and software while ensuring regulatory compliance and patient safety.
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet…
Senior QA engineer in medical diagnostics builds risk-based quality systems, reviews NPI/change controls, and ensures ISO 13485 and 21 CFR 820 compliance for life-saving molecular testing devices.
At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries…
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