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Investigates medical-device failures by parsing software logs, reviewing service reports, and analyzing imaging data to determine root causes and support regulatory-compliant quality improvements.
Be visionary Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory…
Oversee the ISO 9001 quality system and daily shop-floor quality for medical-device manufacturing, ensuring compliance and driving continuous improvement in a regulated environment.
We anticipate the application window for this opening will close on - 13 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore…
Oversee supplier quality for medical devices, ensuring compliance with FDA and ISO standards, and improving supplier performance through audits, corrective actions, and process optimization.
Quality Engineer at Abbott in San Diego ensuring medical device quality compliance, analyzing data, and resolving nonconformances per ISO 13485 and FDA regulations.
Onsite QA specialist in a biopharma facility inspects products and documentation to ensure regulatory compliance and customer requirements are met.
Leads a team to build and scale data analytics for quality compliance and regulatory readiness in medical devices, using SQL and visualization tools to drive risk management and continuous improvement.
Optimizes and sustains manufacturing processes in a medical device facility using lean and Six Sigma tools, ensuring compliance with healthcare regulations and improving efficiency.
Leads quality assurance for medical device development in a regulated environment, ensuring compliance with FDA, ISO, and risk-management standards while mentoring teams and driving continuous improvement.
Who We Are ABOUT ENOVIS™ Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient…
Ensures laboratory equipment meets regulatory standards by managing documentation, compliance audits, and cross-functional validation projects in a precision-medicine healthcare setting.
Onsite quality engineer ensuring medical device manufacturing meets regulatory and quality standards using risk analysis, Six Sigma, and FDA/ISO compliance.
Work Flexibility: Hybrid What you will do - Join a high-impact sourcing team supporting one of Stryker's most critical manufacturing sites. As a Sourcing Manager, you'll drive strategic sourcing initiatives…
Ensures medical devices and software meet strict quality and regulatory standards by investigating issues, improving processes, and supporting manufacturing and new product launches.
Senior Quality Engineer ensures medical device manufacturing meets regulatory standards, resolves production issues, and leads quality improvements using Six Sigma and Lean methodologies.
Design Transfer Scientist at Natera to transition NGS-based IVD assays from R&D into clinical manufacturing, ensuring compliance and scalability while bridging lab work with production pipelines.
Location: On-Site in Boulder, CO (Foresight Dx business unit, a Natera company) Foresight Diagnostics is a molecular diagnostics company pioneering non-invasive cancer detection through highly sensitive, cell-free…
What You’ll Do Reporting to the Chief Financial Officer, you will lead all aspects of IT for approximately 220 employees across two manufacturing sites. Strategy and Leadership Develop and execute LSO's IT strategy…
Grover Precision | Quality Manager | Oxford, Maine Grover Precision , a family-owned business, is seeking a Quality Manager to join its team in Oxford, Maine. Since 1983, Grover has provided precision manufacturing…
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