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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.
About MISUMI Americas MISUMI Americas, a division of MISUMI Group, is a leading provider of standard, configurable, and custom manufacturing solutions. By integrating a vast catalog of components with a world-class…
Oversee training programs and quality assurance initiatives for a biotech company, ensuring employees meet clinical and regulatory standards while improving operational efficiency.
Oversee training programs and quality assurance initiatives to improve operational efficiency and employee performance in a biotech/lab environment, ensuring compliance with healthcare regulations.
Are you ready to work for a company that truly cares about making a meaningful difference in this world? A little about us: Praxis Technology is a manufacturing company that designs and develops titanium parts for…
Date Posted: 2026-08-25

 Country: Singapore

 Location: SG-01-SINGAPORE-039 IHUB ~ 39 Changi N Cres ~ 39 IHUB BLDG

 Position Role Type: Onsite At RTX, the world's…
Quality Assurance Manager role at Takeda Vietnam in Ho Chi Minh City with no further details provided in the posting.
Brooks is a leading provider of automation solutions with over 40 years of experience in the semiconductor industry, offering precision robotics, integrated automation systems, and contamination control solutions that…
ZEISS in India ZEISS in India is headquartered in Bengaluru and present in the fields of Industrial Quality Solutions, Research Microscopy Solutions, Medical Technology, Vision Care and Sports & Cine Optics. ZEISS…
Define and own automated test strategy and frameworks for clinical dashboards, microservices, and data pipelines using C# and Selenium at Philips' Image Guided Therapy Systems division.
Leads quality assurance for Philips’ Pune manufacturing sites, ensuring compliance with FDA/ISO regulations and patient safety. Oversees quality systems, regulatory inspections, and cross-functional collaboration to drive operational excellence and continuous improvement in medical device production.
Designs and owns system architecture for Philips’ Azurion Eye Sensing Lab, integrating hardware, AI, data pipelines, and cloud for real-time clinical workflow automation in regulated medical environments.
Acute Care Technology At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical…
Salary: Up to $5,000/month Employment Type: Permanent Working Hours: Office Hours Job Scope: Lead laboratory operations and supervise Lab Analysts and Technicians Review analytical results, investigate quality issues,…
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for…
Job Summary The Customer Service Representative serves as the primary point of contact for customers by providing exceptional service throughout the order-to-delivery lifecycle. This role is responsible for processing…
The Regional Lead Quality Engineer CP/MD is responsible for leading a regional team comprised of Medical Device and Packaging QA Staff (Advisor) that supports design, development, manufacture, and regulatory approval…
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