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Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to…
Leads quality engineering for AI-powered medical ultrasound devices, ensuring compliance with medical device regulations and driving design controls for hardware and software.
Designs and maintains automated test frameworks to verify software updates on medical devices, ensuring safety and compliance while integrating with hardware and CI pipelines.
Who are we and why should you join us? ConcertAI is building the future of precision medicine. We use advanced artificial intelligence and real-world data to transform how healthcare and life sciences generate…
The Alliance & Market Expansion Manager, North America is responsible for supporting and expanding one of LGC Diagnostics & Genomics' largest and most strategic global partnerships with a market-leading IVD…
Oversee document control and the electronic Quality Management System for a med-tech startup, ensuring regulatory compliance and traceable records for clinical-grade wearables.
Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer electronics engineers…
Coordinates warehouse operations for a medical device company, handling inventory, shipping, and GMP-compliant logistics using ERP systems like D365.
Recruiter: Spencer Gregory Hale Supplier Quality Engineer III – Metals About this role: The Arden Hills Supplier Quality Engineering team is looking for high-energy, driven, passionate people, looking to not just…
The Quality Assurance Technician performs inspections and audits on in-process and finished products to ensure compliance with customer specifications and ISO standards. The role involves maintaining quality documentation, verifying equipment calibration, and supporting production teams in a manufacturing environment.
Recruiter: Spencer Gregory Hale Principal Quality System Engineer - CAPA About the role: As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving…
Additional Location(s): US-MN-Arden Hills; US-MA-Marlborough; US-MN-Maple Grove Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the…
About Sequel Sequel, headquartered in Manchester, New Hampshire, is a company developing the next generation of transformative drug-delivery advancements starting with diabetes. Sequel’s approach is to look at diabetes…
About Company At ENNOVI we harness the power of two megatrends - electrification and AI - to help industries innovate at speed, operate smarter, and achieve sustainable growth. By combining these transformative forces…
Quality Manager MartiDerm | HQ Cervelló (Barcelona) MartiDerm, tú eres la fórmula En MartiDerm llevamos desde 1952 cuidando la salud de la piel a través de la ciencia, la innovación y la dermocosmética de alta…
The Role Rarity Bioscience is looking for a hands-on Quality and Regulatory Manager to help transition our innovative molecular diagnostics technology from research use into clinical practice. This is a broad and…
The QMS Program Manager oversees SharkNinja's Quality Management System for medical devices, guiding New Product Development teams in creating safe and effective devices while ensuring compliance with standards like ISO 13485 and FDA regulations throughout the product lifecycle.
Senior Quality Analyst managing customer complaints, clinical risk assessments, and post-market surveillance for a healthcare diagnostic informatics company, ensuring regulatory compliance using eQMS, risk management tools, and AI-enabled analytics platforms.
Technical Project Manager bridging engineering processes with medical market requirements for an AI-supported capsule endoscopy system, working closely with the CTO on R&D of software, hardware, and medical certification.
Technical Writer owning and authoring regulatory-compliant documentation (architecture, UI specs, risk assessments) for a Software as a Medical Device product, supporting design controls and SDLC activities at an AI-powered medtech company.
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