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BASIC FUNCTION OF THE JOB: Lead a high-performing Plant Maintenance organization to ensure the reliability, availability, safety, compliance, and optimal performance of all manufacturing equipment, automated production…
Oversee supplier quality, incoming inspection, and metrology teams for a medical device manufacturer, ensuring compliance and continuous improvement in a regulated manufacturing environment.
Process Quality Engineer at Qnity in Shenzhen, managing product quality from development through mass production using APQP, PPAP, and quality tools to ensure compliance and continuous improvement.
Senior Industrial Engineer at Illumina in Singapore designs and optimizes high-volume manufacturing workflows using Lean Six Sigma, AutoCAD, and simulation tools to improve quality, efficiency, and cost in genomics production.
The Opportunity: Under moderate supervision, conducts general business support, including handling inquiries from external or internal customers, coordinating resolution of customer issues with internal departments,…
Oversee the transfer of medical-device designs into manufacturing, ensuring compliance with ISO 13485, 21 CFR 820 and other regulations while validating processes and managing risk.
On-site field engineer servicing and repairing ZOLL’s acute-care medical devices (AEDs, ventilators, etc.) at hospitals, ensuring uptime and compliance with FDA/ISO standards.
Safety Engineer ensures medical devices meet safety and regulatory standards by managing risk throughout development and lifecycle.
Integrate, test, and troubleshoot next-generation DNA sequencing systems, combining hardware, fluidics, chemistry, software, and bioinformatics to advance Illumina’s genomic technologies.
Oversee quality and regulatory compliance for medical-device design and development, ensuring adherence to FDA, ISO 13485, and ISO 14971 while partnering with R&D to embed risk management and patient safety.
Ensures medical-device quality by auditing processes, investigating deviations, and enforcing GMP/ISO standards to safeguard patient care in a regulated manufacturing environment.
Leads quality and design transfer for medical devices, ensuring compliance with regulations like ISO 13485 and 21 CFR 820 while coordinating risk management and manufacturing validation.
Quality Engineer in medtech who partners with R&D and manufacturing to ensure medical devices meet safety and regulatory standards through design control, validation, and CAPA processes.
Quality Engineer II at a medical-device startup in Bedford, MA, ensuring implantable hydrogel devices meet regulatory standards through inspections, testing, and process controls.
A Senior Quality Engineer ensures product quality and regulatory compliance for medical devices and membrane products in high-volume manufacturing, using ISO 13485/9001 standards, root-cause analysis (8D/DMAIC), and risk-based tools like PFMEA. They collaborate with R&D, manufacturing, and suppliers to drive continuous improvement and resolve quality issues.
A Senior Process Engineer at Integralife optimizes and sustains manufacturing processes for medical devices using lean and six sigma methodologies, ensuring compliance with regulations like GMP and FDA, while working cross-functionally with teams to improve efficiency and quality.
We anticipate the application window for this opening will close on - 22 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore…
Lead cross-functional engineering programs to develop, industrialize, and launch medical technologies, coordinating teams across Engineering, Manufacturing, Quality, and Supply Chain.
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…
Design Quality Engineer II reviews medical-device design changes, risk assessments, and verification/validation to ensure compliance with ISO 13485, EU MDR, and FDA QMSR while collaborating with R&D and manufacturing teams.
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