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Mfg. Engrs - Project Manager COMPANY OVERVIEW Viant Medical is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life…
Senior QA engineer ensuring medical-device quality via risk management, design controls, and regulatory compliance (FDA 21 CFR 820, ISO 13485) for a diagnostics manufacturer.
Senior DevOps & Release Engineer designs and maintains secure Linux-based DevOps infrastructure for regulated medical software, ensuring compliance with FDA and ISO standards while automating build, release, and deployment pipelines for on-premise clinical systems.
Work Schedule Other Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in…
Design Quality Engineer for medical devices in the Sports Medicine franchise, executing risk management, design controls, and verification/validation per ISO 14971 and IEC 62304.
Senior Software Engineer at Cytiva (Danaher) building and improving life-saving software for cell therapy R&D using C# and C/C++ in a regulated medical-device environment.
We anticipate the application window for this opening will close on - 24 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore…
Imaging Service Engineer III St Louis, MO • Full-time • On-site About Tri Imaging Solutions Tri Imaging Solutions has merged with DirectMed Imaging, uniting two trusted names in the medical imaging industry under one…
Imaging Service Engineer I St Louis, MO • Full-time • On-site About Tri Imaging Solutions Tri Imaging Solutions has merged with DirectMed Imaging, uniting two trusted names in the medical imaging industry under one…
Lead quality-assurance investigations and risk-management for medical devices, ensuring regulatory compliance and patient safety through root-cause analysis and corrective actions.
Ensure compliance and drive improvements for Plexus’s quality management systems, handling audits, corrective actions, and documentation for healthcare and industrial products.


 We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It…
Perform quality assurance reviews of raw materials and batch manufacturing records for oligonucleotide production in a GMP lab, ensuring compliance with ISO 13485 and regulatory standards.
Ensure pharmaceutical manufacturing meets ISO and GMP standards by supporting quality audits, investigations, and documentation for a global life-sciences company.
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our…
Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Join a high performing distribution and operations team where your leadership will directly impact inventory…
Scope: The Senior Computer Systems Validation Engineer is responsible for validation of global computer systems, monitoring changes with regulations, and assists team members for CSI’s corporate Computer Systems…
Career-defining. Life-changing. At iRhythm, you’ll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere…
We anticipate the application window for this opening will close on - 11 Sep 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore…
Lead quality-improvement programs for medical devices, coordinating cross-functional teams to enhance product quality, compliance, and patient outcomes in a regulated healthcare environment.
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