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About 누적 투자액 800억 규모, 시리즈 C 투자 유치 인공지능 기반 웨어러블 의료 솔루션 선두기업 HUINNO 휴이노는 전세계 사망률 1위인 심뇌혈관질환에 맞서고 있는 수많은 환자와 가족, 의료진을 돕는 서비스를 만들고 있습니다. 웨어러블 기기로 주요 생체신호(혈압, 심전도, 심장 박동수 등)를 측정하고, 이를 자체적으로 개발한 인공지능 솔루션으로 분석해 의료진이 신속하고 정확한…
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description This position is responsible for 8 sites globally, > 130 team members, and Quality teams performing critical Quality operational…
Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every…
We anticipate the application window for this opening will close on - 3 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore…
Quality Engineer II ensures medical-device quality by reviewing complaints, leading investigations, and enforcing GMP/ISO standards to safeguard patient care.
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to…


 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…
Job Description Summary The Regulatory Affairs Device Manager (m/f/d) role is a global role within Sandoz Regulatory Affairs. In this role you will be responsible for delivering and maintaining global compliance and…
Oversee quality systems for UPS Healthcare’s freight forwarding, ensuring compliance with regulations and auditing carriers while managing risk and stakeholder communications.
Lead a team to optimize GE Healthcare’s manufacturing lines by applying industrial engineering methods, Lean/Six Sigma, and automation to boost productivity, quality, and throughput in a regulated medical-device environment.
Oversee and improve the quality of parts and materials from external suppliers for a medical-device manufacturer, ensuring compliance with FDA and ISO regulations.
Develops and maintains quality visual aids, conducts audits, and leads root-cause analyses to improve manufacturing processes and yields for Jabil’s clients.
Lead the architecture and testing of next-generation robotic medical systems, coordinating cross-functional teams to ensure requirements coverage and system integration from components to full product launch.
Oversee quality systems and regulatory compliance for medical device manufacturing, ensuring adherence to ISO 13485, FDA QSRs, and other standards while leading quality teams and driving continuous improvement.
Owns product strategy and go-to-market for a new whole-blood collection system, driving roadmaps, competitive analysis, and sales enablement in the life-sciences market.
Design Assurance Engineer at Covaris (PerkinElmer) in Woburn, MA, leading quality and compliance activities for new product development and sustaining engineering in life-science instrumentation and consumables.
Junior Software Engineer embedded in a medical-device R&D team to ensure software validation and regulatory compliance under ISO 13485 and FDA 21 CFR Part 820.
Oversee UPS Healthcare’s carrier certification and quality systems, ensuring compliance with global regulations and conducting supplier audits.
Manufacturing Quality Engineer ensures product quality and process compliance for automated diagnostic instruments in healthcare. Daily tasks include investigating defects, improving manufacturing quality, auditing, and collaborating with engineering and suppliers on validation and regulatory requirements.
Oversee supplier quality for medical devices by auditing vendors, applying ISO 13485/21CFR systems, and using risk tools to ensure compliant materials.
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