Quality Engineer Medical Device Manufacturing at Dynaflex Technologies Inc. Quality Engineer Medical Device Manufacturing at Dynaflex Technologies Inc. in Lake Forest, California Posted in 1 day ago.

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full-time Company Description DynaFlex Technologies Inc. is a global contract manufacturer specializing in catheter assemblies and thermoplastic extrusion for the medical device industry. The Corporate Headquarters in Irvine and Yorba Linda focuses on catheter technology development and advanced melt extrusion. A Rapid Prototyping Lab in Fremont supports quick-turn delivery systems prototyping and process development. The production facility in Taiwan provides turnkey contract manufacturing services for high-volume commercial builds, enabling end-to-end solutions from concept to scaled production. Team members collaborate across locations to deliver high-quality, innovative products to medical device partners worldwide. Role Description The Quality Engineer, Medical Device Manufacturing, is a full-time on-site role based in Irvine, CA. This role is responsible for overseeing product quality in catheter manufacturing, including developing and maintaining quality processes, procedures, and documentation in accordance with medical device regulations. Day-to-day tasks include performing inspections and tests, analyzing quality data and metrics, investigating nonconformances, and implementing corrective and preventive actions (CAPA). The Quality Engineer collaborates closely with engineering, production, and supply chain teams to ensure compliant processes, robust validations, and continuous improvement of manufacturing operations. The role also supports internal and external audits, risk management activities, and alignment with customer and regulatory requirements. Qualifications Demonstrated skills in Quality Engineering and Quality Management for medical device manufacturing. Experience in Quality Control methods, including inspection techniques, testing, and data analysis. Proficiency in Quality Assurance activities, such as documentation control, audits, and compliance with ISO 13485 and FDA regulations. Ability to manage Product Quality, including root cause analysis, CAPA, and continuous improvement initiatives. Bachelor's degree in Engineering, Science, or a related technical field; advanced degree or relevant certifications (e.g., CQE) are a plus. Familiarity with catheter manufacturing processes, extrusion, and cleanroom production environments preferred. Experience with validation (IQ/OQ/PQ), statistical process control, and risk management tools (e.g., FMEA). Strong communication skills and ability to work collaboratively with cross-functional teams in a regulated environment.